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  • Inorganic Chemistry  (8,901)
  • 42.75
  • Industrial Chemistry
  • 2015-2019  (47)
  • 1980-1984  (3,506)
  • 1975-1979  (4,160)
  • 1950-1954  (2,931)
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  • 1
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2017-02-10
    Description: Author: Jake Yeston
    Keywords: Inorganic Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2017-01-27
    Description: Author: Jake Yeston
    Keywords: Inorganic Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2017-01-27
    Description: Polynitrogens have the potential for ultrahigh-performing explosives or propellants because singly or doubly bonded polynitrogens can decompose to triply bonded dinitrogen (N2) with an extraordinarily large energy release. The large energy content and relatively low activation energy toward decomposition makes the synthesis of a stable polynitrogen allotrope an extraordinary challenge. Many elements exist in different forms (allotropes)—for example, carbon can exist as graphite, diamond, buckyballs, or graphene. However, no stable neutral allotropes are known for nitrogen, and only two stable homonuclear polynitrogen ions had been isolated until now—namely, the N3− anion (1) and the N5+ cation (2). On page 374 of this issue, Zhang et al. (3) report the synthesis and characterization of the first stable salt of the cyclo-N5− anion, only the third stable homonuclear polynitrogen ion ever isolated. Author: Karl O. Christe
    Keywords: Inorganic Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.115
    Publication Date: 2018-12-13
    Description: Oligochaete wormen komen vooral in zoet water voor. Maar in brak water en zelfs in de volle zee komen enkele soorten voor. Bij onderzoek naar marien benthos werden deze dieren traditioneel niet tot op soort gedetermineerd, omdat ze klein en lastig te determineren zijn. Ze zijn echter niet veel lastiger dan de nauw verwante Polychaeta, die ook hele kleine vertegenwoordigers kennen. In dit artikel wordt een overzicht gegeven van de 32 soorten die nu uit het zoute water in ons land bekend zijn, waarvan er hier zes als nieuw voor de Nederlandse fauna gepresenteerd worden. De vondst van Heterodrilus subtilis in de Noordzee is zeer bijzonder, omdat deze soort verder alleen bekend is van het typemateriaal, dat ongeveer honderd jaar geleden in de Golf van Napels werd verzameld.
    Keywords: Oligochaeta ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 5
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.87
    Publication Date: 2018-12-13
    Description: Het laatste overzicht van de wantsen van de Nederlandse waddeneilanden dateert van 2012. Een opsomming wordt gegeven van 43 nieuwe eilandrecords, waaronder vijf soorten die voor het eerst op de waddeneilanden zijn waargenomen. In totaal zijn er nu 380 soorten wantsen van de Nederlandse waddeneilanden bekend.
    Keywords: Heteroptera ; Nederland ; Waddeneilanden ; verspreiding ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 6
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.57
    Publication Date: 2018-12-13
    Description: Een overzicht wordt gegeven van waarnemingen van 33 soorten nieuwe of anderszins interessante soorten wantsen. Psallus aethiops (Miridae), Empicoris rubromaculatus (Reduviidae), Arocatus melanocephalus, Lygaeus simulans, Eremocoris fenestratus (Lygaeidae) en Nezara viridula (Pentatomidae) zijn nieuw voor de Nederlandse lijst, die daarmee nu 640 soorten telt. Naast nieuwe waarnemingen van zeldzame soorten wordt de recente uitbreiding van Cymatia rogenhoferi (Corixidae), Cardiastethus fasciiventris (Anthocoridae), Arocatus longiceps en Rhyparochromus vulgaris (Lygaeidae), Leptoglossus occidentalis (Coreidae), en Peribalus strictus en Rhaphigaster nebulosa (Pentatomidae) in kaart gebracht.
    Keywords: Heteroptera ; Nederland ; verspreiding ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 7
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.101
    Publication Date: 2018-12-13
    Description: In Nederland komen tien soorten ruighaarkevers (genera Dryops en Pomatinus) voor. Ze leven langs oevers van stilstaande en stromende wateren. Het was een verrassing toen in 2014 een vrouwtje van de zeer zeldzame Dryops striatellus gevonden werd bij Bakkeveen (provincie Friesland). De soort was sinds 1960 niet meer in Nederland gevonden. In 2016 werd D. striatellus op een tweede locatie nabij Bakkeveen gevonden. In dit artikel geven wij informatie over de soort en presenteren bijzonderheden over de Friese populatie en haar habitat.
    Keywords: Coleoptera ; Dryopidae ; Dryops striatellus ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 8
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.11
    Publication Date: 2018-12-13
    Description: Op 14 oktober 2015 werd een halmvlieg met fraaie zwarte vlekken op de vleugels gefotografeerd in Hoogerheide (Noord-Brabant). Na vergelijking van foto’s werd geconcludeerd dat het moest gaan om Gampsocera numerata, welke determinatie later werd bevestigd. Reeds in 2009 bleek in België een mannetje van de soort gefotografeerd te zijn in een tuin in Evere. Ook in 2010 en 2015 is de soort in België gevonden. Dit zijn de eerste meldingen van G. numerata voor Nederland en België.
    Keywords: Diptera ; Chloropidae ; Gampsocera numerata ; Nederland ; België ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 9
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.49
    Publication Date: 2018-12-13
    Description: Recently two exotic tubeworms new to the fauna of the Netherlands have been recorded in inshore waters in the delta area: Desdemona ornata and Pseudopolydora paucibranchiata. Within the Polychaeta these worms belong to the group of the Sedentaria. These construct a tube, in which the body of the worm is hidden. The head and feeding appendages protrude from the opening. Most probably these tubes are a major factor in the transport of these animals around the world, as they provide excellent shelters when they are attached to the hull of a ship or commercially traded shellfish.
    Keywords: Polychaeta ; Pseudopolydora paucibranchiata ; Desdemona ornata ; Nederland ; verspreiding ; exoot ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 10
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.31
    Publication Date: 2018-12-13
    Description: De boszandbij Andrena coitana leek verdwenen uit Nederland. Veertig jaar na de laatste waarneming in 1975 is weer een populatie van deze soort gevonden, bij Epe in Gelderland. De boszandbij is een kleine soort, die mogelijk nog op sommige plaatsen over het hoofd gezien is. In dit artikel wordt de kennis over deze bijzondere bij samengevat en gespeculeerd over de oorzaken van de achteruitgang in Nederland.
    Keywords: Hymenoptera ; Apidae ; Andrena coitana ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 11
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.1
    Publication Date: 2018-12-13
    Description: In 2015 werd Kelisia monoceros voor het eerst in ons land verzameld bij Kamperland in Zeeland. Deze spoorcicade leeft op de algemeen voorkomende valse voszegge. De vondst wijst op een recente areaaluitbreiding. Een andere spoorcicade, Ditropsis flavipes, werd al eerder uit ons land gemeld, maar verspreidingsgegevens worden nu voor de eerste maal gepubliceerd. Ditropsis flavipes leeft monofaag op bergdravik, een in Nederland zeldzaam gras.
    Keywords: Homoptera ; Delphacidae ; Nederland ; verspreiding ; biologie ; Kelisia monoceros ; Ditropsis flavipes ; herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 12
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.17
    Publication Date: 2018-12-13
    Description: Alle spinnen hebben gif in hun kaken om hun prooien te doden. Verreweg de meeste soorten kunnen de menselijke huid niet doorboren met hun kaken en zijn dus volkomen ongevaarlijk. Kogelspinnen uit het genus Latrodectus, oftewel weduwen, vormen een uitzondering. Deze exotische spinnen worden af en toe geïmporteerd in Nederland. In 2013 is het aantal vondsten van geïmporteerde Latrodectus-spinnen op een rij gezet in een risicobeoordeling, met als resultaat een lijst van tien records met bewijsmateriaal. Hier kunnen nu vier records aan toegevoegd worden. Hieronder bevindt zich een vondst van de bruine weduwe L. geometricus, die recent voor het eerst in ons land werd vastgesteld, en een eerste geval van uitgekomen eitjes van een Latrodectus in ons land, van de roodrugspin L. hasselti.
    Keywords: Araneae ; Theridiidae ; Latrodectus ; Nederland ; exoot ; verspreiding ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 13
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.27
    Publication Date: 2018-12-13
    Description: In 2015 werd tijdens een monitoringsproject van mariene bodemfauna op het Friese front de vulkaanworm Maxmuelleria lankesteri aangetroffen. Dit is de eerste vondst in Nederlandse wateren. De vulkaanworm dankt zijn naam aan de vorm van de opening van zijn leefgang, een vulkaanachtige slibheuvel. Het is opmerkelijk dat deze grote, opvallende worm (12-18 cm lang) niet eerder is aangetroffen. Mogelijk ligt dit aan de ongebruikelijke bemonsteringsmethode. Anderzijds kan de vulkaanworm daadwerkelijk zeldzaam zijn.
    Keywords: Echiura ; Maxmuelleria lankesteri ; Nederland ; verspreiding ; herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 14
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.95
    Publication Date: 2018-12-13
    Description: De kleine bleekvlekwespbij Nomada baccata behoort tot een complex van taxa rond de bleekvlekwespbij Nomada alboguttata. De kleine bleekvlekwespbij is vroeger verspreid over het land aangetroffen, maar de laatste waarneming dateerde alweer van 1992. In de afgelopen jaren werd de soort op twee plekken in ons land teruggevonden, in de Schoorlse duinen in Noord-Holland in 2012 en op de Tongerense hei bij Epe in Gelderland in 2015.
    Keywords: Hymenoptera ; Apidae ; Nomada baccata ; taxonomie ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 15
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.37
    Publication Date: 2018-12-13
    Description: De familie der sluipvliegen is één van de soortenrijkste vliegenfamilies in ons land. De larven ontwikkelen zich inwendig in ongewervelden, veelal vlinderrupsen. De groep is in ons land relatief goed bestudeerd en de afgelopen jaren zijn diverse aanvullingen op de checklist uit 2002 gepubliceerd. In dit artikel worden wederom twee soorten voor het eerst uit ons land vermeld. Hiermee komt het totaal aantal soorten dat in Nederland is vastgesteld op 336. Daarnaast wordt de herontdekking van een soort beschreven die al meer dan een eeuw niet meer waargenomen was.
    Keywords: Diptera ; Tachinidae ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 16
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.15
    Publication Date: 2018-12-13
    Description: Canacidae zijn gebonden aan de kust en zou je daarmee typisch Nederlandse vliegjes kunnen noemen. In dit artikel melden wij een nieuwe soort van deze familie: Canace nasica en presenteren we een nieuwe Nederlandse checklist voor de familie. Naar de nieuwste taxonomische inzichten wordt daarbij de familie Tethinidae als subfamilie onder de Canacidae toegevoegd. Hiermee is de Nederlandse fauna een vliegenfamilie armer.
    Keywords: Diptera ; Canacidae ; Canace nasica ; Nederland ; herkenning ; verspreiding ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 17
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.11
    Publication Date: 2018-12-13
    Description: De kassprinkhaan is een buitenbeentje onder de Nederlandse sprinkhanen en krekels. Ze komt van oorsprong waarschijnlijk voor in grotten in Oost-Azië en is door transport van eieren met plantenmateriaal over de hele wereld verspreid geraakt. Ze kan tijdelijk overleven in het kunstmatig grotmilieu van bijvoorbeeld kruipruimtes van woonhuizen, in kassen en tuincentra. Recentelijk werd een opmerkelijk grote populatie van de kassprinkhaan gevonden in het uitgebreide stelsel aan kruipruimtes onder een verpleeghuis in Friesland. De kassprinkhaan blijkt hier al ruim 40 jaar voor te komen. Het is waarschijnlijk de grootste Europese populatie van deze soort.
    Keywords: Orthoptera ; Diestrammena asynamora ; verspreiding ; exoot ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 18
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    In:  Nederlandse Faunistische Mededelingen (0196-2453) vol.46 (2016) p.43
    Publication Date: 2018-12-13
    Description: In het kader van het project ‘Duik de Noordzee Schoon’ worden scheepswrakken onderzocht, beschreven en van afval ontdaan. Scheepswrakken vormen een bijzonder leefgebied in het mariene milieu, met een hoge biodiversiteit. Dit bleek weer tijdens onderzoek van visnetten die van ver weg gelegen wrakken waren verwijderd. Hierbij werden maar liefst vier nieuwe mosdiertjes voor de Nederlandse fauna aangetroffen.
    Keywords: Bryozoa ; Nederland ; verspreiding ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 19
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.43
    Publication Date: 2018-12-13
    Description: Pauropoda of weinigpoten zijn nauw verwant aan de miljoenpoten en duizendpoten. Het is een weinig bestudeerde diergroep, die bestaat uit kleine, witte en blinde bodemdieren die nauwelijks opvallen. Het meest kenmerkende zijn de gevorkte antennen, die wat bouw betreft uniek zijn ten opzichte van andere ongewervelden. Er zijn slechts acht soorten gemeld uit Nederland, alle behorend tot het genus Allopauropus. Recentelijk is een nieuwe soort, uit het genus Pauropus, in het westen van het land aangetroffen. Het betreft dus ook een nieuw genus voor de Nederlandse fauna. In dit artikel wordt de nieuwe soort voorgesteld, beschrijven we de habitat en geven we informatie over de verspreiding.
    Keywords: Myriapoda ; Pauropoda ; Pauropus lanceolatus ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 20
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.46 (2016) p.19
    Publication Date: 2018-12-13
    Description: Slakkendodende vliegen (familie Sciomyzidae) zijn al niet zo opvallend in het veld, maar de soorten uit de genera Pherbellia en Ditaeniella worden nog minder gevonden, mede doordat ze vrij klein zijn. De 14 Nederlandse soorten lijken sterk op elkaar. Dit artikel biedt een tabel om ze te kunnen herkennen en geeft informatie over ecologie en verspreiding.
    Keywords: Diptera ; Sciomyzidae ; Pherbellia ; Ditaeniella ; Nederland ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 21
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.1
    Publication Date: 2018-12-13
    Description: Platwormen komen in Nederland vooral voor in zoet water, maar er zijn twee soorten van landbiotoop bekend. De laatste jaren duiken steeds vaker exotische landplatwormen op in Europa, vooral in kassen en tuincentra, maar sommige kunnen ook buitenshuis overleven. Uit Nederland zijn Bipalium kewense, Caenoplana bicolor en Marionfyfea adventor gemeld. Omdat ze regenwormen en slakken eten, kunnen ze een grote invloed hebben op het bodemleven, met gevolgen voor natuurlijke ecosystemen en landbouwgebieden. In het buitenland is de aandacht voor exotische landplatwormen al groeiende. Zo wordt de Nieuw-Guineese landplatworm Platydemus manokwari door de IUCN tot de 100 ergste invasieve soorten aangemerkt. In Nederland is er nog nauwelijks aandacht voor landplatwormen. Daarom wordt in dit artikel de kennis over deze groep samengevat.
    Keywords: Platyhelminthes ; Tricladida ; Nederland ; verspreiding ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 22
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.39
    Publication Date: 2018-12-13
    Description: Blaaskopvliegen zijn een van de groepen uit het atlasproject Leuke vliegen, dat in 2015 werd afgesloten. Het zijn over het algemeen opvallend gekleurde vliegen, die parasiteren bij bijen en wespen. In een overzichtsartikel uit 2014 werd de komst van Leopoldius calceatus al voorspeld en in 2015 werd soort inderdaad aangetroffen in Groeve Craubeek in de provincie Limburg en een jaar later op de Stratumse heide bij Eindhoven.
    Keywords: Diptera ; Conopidae ; Nederland ; Leopoldius calceatus ; verspreiding ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 23
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.47 (2016) p.49
    Publication Date: 2018-12-13
    Description: Astigmatic mites probably form the most diverse cohort of mites. At present the former order of Astigmatina is ranked within the suborder Oribatida or moss mites. However astigmatic mites occupy a much wider range of habitats than other oribatid mites: from marine coasts to stored food, plant bulbs and houses. The vast majority live as commensals or parasites on a variety of hosts, ranging from insects to birds and mammals, inhabiting the fur, feathers, skin and even lungs and stomach. This first checklist for the Netherlands contains 262 species, but many more are to be expected. Brief data on occurrence and nomenclature are provided for each species.
    Keywords: Acari ; Oribatida ; Astigmatina ; verspreiding ; taxonomie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 24
    Publication Date: 2016-02-09
    Description: Wing shape variation was investigated between the sexes and among four populations of the scorpionfly Dicerapanorpa magna (Chou, 1981) endemic to the Qin-Ba Mountains area, China through the landmark-based geometric morphometric approach. The results show that sexual dimorphism exists both in wing size and shape in D. magna. Significant differences exist in female wing size and shape among D. magna populations. The possible reasons of the wing variation are discussed based on the divergence time of D. magna in combination with the tectonic and climatic events in the Qin-Ba Mountains during the late Miocene-Pleistocene period. Whether reproductive isolation exists between different populations needs further research.
    Keywords: canonical variates analysis ; individual variation ; sexual dimorphism ; 42.75 ; 42.62
    Repository Name: National Museum of Natural History, Netherlands
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  • 25
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2016-09-09
    Description: Author: Jake Yeston
    Keywords: Inorganic Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 26
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2016-11-11
    Description: Author: Jake Yeston
    Keywords: Inorganic Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 27
    Publication Date: 2017-12-07
    Description: In Nederland zijn natuurlijke en semi-natuurlijke graslanden relatief slecht onderzocht op de aanwezigheid van springstaarten. In de ons omringende landen zijn deze biotopen vaak rijk aan specifieke soorten die alleen daar voorkomen. Naar verwachting kunnen in dit milieu veel nieuwe soorten voor onze fauna gevonden worden, vooral op nutriëntarme, zandige en droge ondergrond. Recentelijk zijn twee soorten uit het genus Folsomides in graslanden in het zuiden van ons land aangetroffen. Het betreft hier een nieuw genus voor de Nederlandse fauna. In dit artikel worden het genus en de twee soorten voorgesteld, beschrijven we de habitat en geven we informatie over de verspreiding en begeleidende soorten van deze springstaarten.
    Keywords: Collembola ; Isotomidae ; Folsomides ; verspreiding ; Nederland ; herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 28
    Publication Date: 2017-12-07
    Description: Psilota is een genus van kleine, zwarte zweefvliegen, waarvan de larven leven achter boomschors. In 1988 werd Psilota anthracina voor het eerst in Nederland waargenomen en lange tijd is het een zeldzame soort geweest. De laatste jaren wordt ze steeds algemener, vermoedelijk door een veranderd bosbeheer. Gaandeweg is gebleken dat er een tweede soort onder schuilging; P. atra. Toen in België een derde soort opdook was het wachten tot deze ook in Nederland aangetroffen zou worden. In 2012 was het zover. Als Nederlandse naam stellen we voor spichtige spitsbek.
    Keywords: Diptera ; Syrphidae ; Psilota ; verspreiding ; Nederland ; herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 29
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.51
    Publication Date: 2017-12-07
    Description: Het voorkomen van Badonnelia titei in ons land wordt in enkele publicaties genoemd. Deze exoot blijkt niet zeldzaam in archiefdepots overal in Nederland. In deze publicaties werd echter geen aandacht besteed aan het feit dat de soort nog niet als nieuw voor Nederland was gemeld, waar bewijsexemplaren zijn ondergebracht en hoe B. titei te herkennen is. De soort is daarom dan ook nooit doorgedrongen tot de diverse faunaoverzichten van Nederlandse stofluizen. Reden genoeg om deze zaken te behandelen in dit artikel, waarbij tevens een vindplaatsenkaartje wordt gegeven en de eerste vondsten uit woonhuizen worden gemeld.
    Keywords: Psocodea ; Sphaeropsocidae ; Badonnelia titei ; verspreiding ; Nederland ; exoot ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 30
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.44 (2015) p.1
    Publication Date: 2017-12-07
    Description: De omgeving van Ommen en Hardenberg is het enige gebied in Nederland waar alle vier de soorten rode bosmieren voorkomen, waaronder de in Noordwest-Europa zeer zeldzame stronkmier. Recent is aan de alarmbel getrokken omdat het niet goed gaat met deze soort. Aanleiding voor een nieuw onderzoek bij Ommen, waarbij alle bosmieren onder de loep zijn genomen.
    Keywords: Hymenoptera ; Formicidae ; Formica ; verspreiding ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 31
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    In:  Contributions to Zoology (1875-9866) vol.84 (2015) nr.4 p.305
    Publication Date: 2015-12-07
    Description: Firm coupling of genitalia is critical for copulation in most groups of insects. To counter female resistance that usually breaks off genital connection, male scorpionflies (Mecoptera: Panorpidae) usually provide nuptial gifts for the female and seize their mates with grasping devices. The notal organ, a modified clamp on tergum III of male scorpionflies, plays a significant role in seizing the female wings and helping maintain mating position during copulation. The mating behaviour remains unknown for the scorpionfly Furcatopanorpa longihypovalva (Hua and Cai, 2009) whose male lacks a notal organ. In this paper, we first attempt to study the mating behaviour of F. longihypovalva. The results show that the male provides liquid salivary secretion through a mouth-to-mouth mode for the female, and maintains copulation mainly by continuous provision of salivary secretion rather than by seizing the female with grasping devices. Thus the male copulates with the female in an atypical O-shaped position, with only their mouthparts and genitalia connected to each other. The salivary glands exhibit remarkable sexual dimorphism: short and bifurcated in the female, but well-developed and multi-furcated in the male. The extremely developed salivary glands of the male lay a structural foundation for the male to continuously provide liquid salivary secretion, and to help the male to mediate female resistance, being likely to serve as a compensation to his absence of the notal organ. We also investigated the functional morphology and copulatory mechanism of the male and female genitalia. The evolution of the atypical mating pattern of F. longihypovalva is putatively discussed as an adaptation in the context of sexual conflict.
    Keywords: Mecoptera ; Panorpidae ; Furcatopanorpa longihypovalva ; mating behaviour ; nuptial feeding, ; salivary glands ; genitalia ; functional morphology ; copulation ; 42.75 ; 42.62
    Repository Name: National Museum of Natural History, Netherlands
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  • 32
    Publication Date: 2015-11-10
    Description: Female genitalia are widely underrepresented in taxonomic studies. Here we investigate the morphological variation among female copulation organs for a group of scarab beetles (Sericini) with similar ecology, external morphology and copulation mechanics. We examined traits qualitatively and quantitatively based on 80 and 18 species (genus Pleophylla), respectively. Additionally we explored whether female genitalia are affected by asymmetry. The vast diversity of slerotised structures including their shapes illustrated the high taxonomic and phylogenetic utility of female genitalia in this group. The morphometric analysis of Pleophylla, confirmed that sclerotisations in the ductus bursae are very suitable for species-level taxonomic purposes. Stable interspecific variation is more hardly discernable in other parts such as the vaginal palps (shape and size) or the other membranous structures such as the shape of the bursa copulatrix. Asymmetric genitalia that arose multiple times independently among insects are found in most of the examined Sericini species. Asymmetries regarded either the bursa copulatrix, or both the bursa copulatrix and ductus bursae and comprised sclerotised and non-sclerotised structures being most common in modern Sericini. Here, highly asymmetric sclerotised structures are linked with strong asymmetry of the male copulation organs. Widespread asymmetry among megadiverse Sericini with a complex male-female genital asymmetry suggests that the shift to asymmetry is phylogenetically rather conserved. From the range of hypotheses, sexual selection seems to be the most reasonable to explain the evolution and stability of asymmetry in chafer genitalia.
    Keywords: beetles ; female genitalia ; integrative taxonomy ; Melolonthinae ; morphology ; 42.75 ; 42.64 ; 42.62
    Repository Name: National Museum of Natural History, Netherlands
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  • 33
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.39
    Publication Date: 2017-12-07
    Keywords: Coleoptera ; Brentidae ; Exapion ulicis ; verspreiding ; Nederland ; herkenning ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 34
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.44 (2015) p.11
    Publication Date: 2017-12-07
    Description: Eikelwormen zijn mariene wormen die een eigen klasse vormen, de Enteropneusta. In Nederland zijn het ook de enige vertegenwoordigers van de kraagdragers (fylum Hemichordata). Het zijn bijzondere dieren, die nauwer verwant zijn aan stekelhuidigen en gewervelde dieren dan aan gelede wormen. Het lichaam is ongeleed, met een gesteelde slurf, met daarachter een kraag en een langwerpig lichaam met tientallen kieuwspleten. De wormen leven in een U-vormige buis in zachte bodems. In de loop van de tijd zijn wel eikelwormen langs de Nederlandse kust verzameld, maar deze zijn nooit op naam gebracht. In dit artikel wordt ingegaan op de eerste vondsten van eikelwormen in de Oosterschelde.
    Keywords: Enteropneusta ; Saccoglossus ; verspreiding ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 35
    facet.materialart.
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.44 (2015) p.47
    Publication Date: 2017-12-07
    Description: The gall midges are one of the most important groups of gall makers. Emerging larvae produce stimuli and the host plant responds by producing galls, fascinating structures which provide food and shelter for the developing larvae. Most gall inducing midges are host specific: they are only able to induce galls in a few, often related, plant species. A few species have different feeding modes: among them are saprophagous, fungivorous and predaceous species and some are used in biocontrol. We recorded 416 species in the whole area; 366 species are recorded from the Netherlands, 270 species from Belgium and 96 species from Luxembourg.
    Keywords: Diptera ; Cecidomyiidae ; Netherlands ; Belgium ; Luxembourg ; distribution ; biology ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 36
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.19
    Publication Date: 2017-12-07
    Description: Het gebeurt met enige regelmaat dat er boorvliegen versleept worden met plantaardige producten. De meeste schadelijke soorten komen uit de tropen en kunnen zich niet handhaven in Nederland. Noord-Amerikaanse soorten van het genus Rhagoletis kunnen in het klimatologisch vergelijkbare Europa wel voet aan de grond krijgen. Eerder bleek dit al met de Oost-Amerikaanse kersenboorvlieg en nu staat hetzelfde te gebeuren met de walnootboorvlieg.
    Keywords: Diptera ; Tephritidae ; Rhagoletis completa ; verspreiding ; herkenning ; Nederland ; exoot ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 37
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.13
    Publication Date: 2017-12-07
    Description: Door gebruik te maken van observatiekunstnestjes is het mogelijk om regelmatig een kijkje te nemen in de nesten van bijvoorbeeld graafwespen. Zij gebruiken de nesten om zich voort te planten. Zo kunnen we meer te weten komen over hun gedrag in het nest tijdens de voortplanting. In dit artikel worden de ervaringen met de graafwesp Psenulus fuscipennis beschreven. De verschillen in levenswijze met de kleine zeefwesp en bijenwolf worden toegelicht.
    Keywords: Hymenoptera ; Crabronidae ; Psenulus fuscipennis ; biologie ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 38
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.7
    Publication Date: 2017-12-07
    Description: De gele tubebij Stelis signata was sinds 1977 niet meer in ons land aangetroffen. Men dacht daarom dat deze bij uit ons land verdwenen was. In 2013 werd de soort echter op Waarneming.nl gemeld van de Strabrechtse hei en in 2014 van Afferden. In 2015 werd een vrouwtje gevangen op de Sprengenberg op de Sallandse heuvelrug. In 2011 heeft Natuurmonumenten hier kleinschalige maatregelen uitgevoerd voor specifieke heidesoorten, waaronder de aanleg van een flink aantal steilranden. Het microreliëf dat daarbij ontstaat vormt een belangrijke nestelplaats voor bijen en wespen. De vondst van de zeldzame gele tubebij op een van deze steilranden vormt de kroon op het werk.
    Keywords: Hymenoptera ; Megachilidae ; Stelis signata ; verspreiding ; biologie ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 39
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.44 (2015) p.37
    Publication Date: 2018-12-13
    Description: In 2007 werd Diplocoelus fagi bij Wageningen gevonden. De larven van deze kever leven in dood hout. Na de eerste vondst zijn diverse andere waarnemingen gedaan en D. fagi is nu bekend uit vier provincies. Omdat de soort in de omringende landen al lang bekend was, is deze late ontdekking opmerkelijk. Mogelijk hangt dit samen met het verbeterde bosbeheer, waarbij minder dood hout uit de bossen wordt verwijderd.
    Keywords: Coleoptera ; Biphyllidae ; Diplocoelus fagi ; verspreiding ; Nederland ; biologie ; herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 40
    facet.materialart.
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    In:  Nederlandse Faunistische Mededelingen (42.75) vol.44 (2015) p.29
    Publication Date: 2017-12-07
    Description: The snail-killing fly Salticella fasciata was discovered in Belgium in 2010. Since then, several new localities on the Belgian coast were discovered and in 2014, the first record for the Netherlands was found. This is the first representative of the genus and also of the subfamily Salticellinae in the Netherlands. In this paper, records from Belgium and the Netherlands are reviewed and information on biology and habitats is summarised.
    Keywords: Diptera ; Sciomyziidae ; Salticella fasciata ; Nederland ; België ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 41
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.44 (2015) p.17
    Publication Date: 2017-12-07
    Description: Twaalf jaar geleden waren er nog geen Nelima-soorten bekend uit ons land. In 2004 en 2006 werden respectievelijk N. sempronii en N. doriae ontdekt. Beide soorten komen ten zuidoosten van ons land voor, en hebben naar alle waarschijnlijkheid Nederland recent bereikt. In 2012 werd op de Maasvlakte een derde vertegenwoordiger van dit genus gevonden: Nelima gothica. De vindplaats lijkt te wijzen op introductie door de mens. Gezien het voorkomen in de ons omringende landen is echter niet uit te sluiten dat hij van oudsher tot onze fauna behoort of recent op eigen kracht Nederland heeft bereikt. Hij zou op meer plaatsen langs de kust kunnen voorkomen. We presenteren de nieuwe soort en geven een overzicht van de vier Noordwest-Europese Nelima-soorten.
    Keywords: Opiliones ; Nelima ; verspreiding ; Nederland ; Europa ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 42
    facet.materialart.
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.1
    Publication Date: 2018-12-13
    Description: Goudwespen zijn fraaie insecten, met felle metaalkleuren in de tinten rood, groen en blauw. Ze parasiteren vaak bij bijen en angeldragende wespen. In dit artikel wordt de eerste vondst van Chrysis equestris voor Nederland beschreven, waarmee het aantal in Nederland gevonden soorten nu op 57 komt. Deze goudwesp parasiteert bij de plooivleugelwesp Discoelius zonalis. Ze wordt in haar hele areaal weinig gevangen.
    Keywords: Hymenoptera ; Chrysididae ; Chrysis equestris ; verspreiding ; biologie ; herkenning ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 43
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.91
    Publication Date: 2017-12-07
    Description: The Flevopark is one of the most special green areas of Amsterdam with a rich nature. Twelve oribatid mite species were collected here in 2014 from bark and mosses on trees. Liacarus acutus and Perlohmannia dissimilis are reported for the first time from the Netherlands. It is not clear if the newly recorded species have always been overlooked or are recent immigrants.
    Keywords: Acari ; Oribatida ; distribution ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 44
    facet.materialart.
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.77
    Publication Date: 2017-12-07
    Description: Watermijten zijn kleine spinachtige diertjes, die in zoet water leven. De aandacht voor deze diergroep is groot, omdat ze een rol spelen in de waterkwaliteitsbeoordeling. In de verspreidingsatlas uit 2000 worden 234 Nederlandse watermijten gemeld. Sinds die tijd worden regelmatig aanvullingen gerapporteerd. In dit artikel worden weer acht nieuwe soorten gemeld, wat het totaal nu op 266 brengt. Dit is een opmerkelijke toename van 13 % in 15 jaar.
    Keywords: Acari ; Hydrachnidia ; verspreiding ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 45
    facet.materialart.
    Unknown
    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.67
    Publication Date: 2017-12-07
    Description: De publicatie van de naamlijst van de Nederlandse kieuwpootkreeften in 2002 was een grote stimulans voor nieuw onderzoek. Na de publicatie met aanvullingen in 2009 zijn er weer negen soorten bijgekomen, waarmee het totaal aantal soorten kieuwpootkreeften in Nederland nu op 124 komt. In dit artikel worden de nieuwe soorten besproken en wordt ingegaan op de redenen voor deze opmerkelijke uitbreiding.
    Keywords: Crustacea ; Branchiopoda ; Cladocera ; Nederland ; verspreiding ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 46
    facet.materialart.
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    In:  Nederlandse Faunistische Mededelingen (0169-2453) vol.45 (2015) p.33
    Publication Date: 2017-12-07
    Description: Prachtvliegen zijn vrij kleine vliegen die vaak een vleugeltekening hebben waardoor ze aan boorvliegen doen denken. De meeste soorten zijn weinig opvallend in het veld aanwezig en zitten vooral op hun waardplanten. Alleen de soorten waarvan de larven leven onder schors van boomstammen zijn opvallender aanwezig door hun balts of territoriaal gedrag. Ze proberen hun stukje boomstam te claimen door snel op en neer te lopen en tegelijkertijd driftig met hun vleugels te bewegen. Tot nog toe was de zeer fraaie Myennis octopunctata (Coquebert, 1798) de enige houtbewonende prachtvlieg in Nederland. In dit artikel wordt daar Homalocephala biumbrata aan toegevoegd.
    Keywords: Diptera ; Ulidiidae ; Homalocephala biumbrata ; verspreiding ; Nederland ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 47
    Publication Date: 2015-11-07
    Description: Integrative taxonomy tests the validity of taxa using methods additional to traditional morphology. The existence of two different morphotypes in specimens identified as Chrysotoxum vernale Loew (Diptera: Syrphidae) prompted their taxonomic study using an integrative approach that included morphology, wing and male-surstylus geometric morphometrics, genetic and ecological analyses. As a result, a new species is recognised, Chrysotoxum montanum Nedeljković & Vujić sp. nov., and C. vernale is re-defined. A lectotype and paralectotypes are designated for C. vernale to stabilize this concept. An additional species, Chrysotoxum orthostylum Vujić sp. nov., with distinctive male genitalia is also described. The three species share an antenna with the basoflagellomere shorter than the scape plus pedicel and terga with yellow fasciae not reaching the lateral margins. This study confirms the value of integrative approach for resolving species boundaries.
    Keywords: Balkan Peninsula ; C. montanum sp. nov. ; C. orthostylum sp. nov. ; ecological niche ; geometric morphometry ; lectotype ; mtDNA COI sequences ; Syrphinae ; 42.75 ; 42.64 ; 42.62
    Repository Name: National Museum of Natural History, Netherlands
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  • 48
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 187-190 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Komplexe von Halogeniden der IV. Gruppe mit einzähnigen Schiffschen BasenVerschiedene Komplexe, die bei der Reaktion von N-(phenyl)benzalaldimin und seinen Derivaten mit einer Methylgruppe in verschiedenen Positionen des Anilinringes mit Halogeniden der IV. Gruppe, MX4, (M = Si bzw. Sn und X = Cl bzw. Br) entstehen, wurden hergestellt und mittels UV-, IR- und Raman-Spektren charakterisiert.
    Notes: Coordination compounds resulting from the interaction of N-(phenyl)benzalaldimine and its derivatives containing a methyl group in different positions of the aniline ring and group(IV) halides, MX4 (where M = Si or Sn and X = Cl or Br), have been prepared and characterized by elemental analyses and electronic, infrared and Raman spectra.
    Additional Material: 4 Tab.
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  • 49
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 208-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 50
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 509 (1984), S. 38-52 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus. 134. On the Triphosphanes H(t-BuP)3H' Li(t-BuP)3Li, and Me3Si(t-BuP)3SiMe3The reaction of 1,3-diiodo-1,2,3-tri-tert-butyltriphosphane, I(t-BuP)3I, with lithium aluminium hydride leads to 1,2,3-tri-tert-butyltriphosphane, H(t-BuP)3H (1). 1 reacts with n-butyllithium to 1,3-dilithium-1,2,3-tri-tert-butyltriphosphide, Li(t-BuP)3Li (2), which reacts further with trimethylchlorosilane yielding 1,3-bis(trimethylsilyl)-1,2,3-tri-tert-butyltriphosphane, Me3Si(t-BuP)3SiMe3 (3). The triphosphanes 1, 2 and 3 could be isolated in a pure state. In solution 1 forms the threo, threo and the threo,erythro configurated diastereomers 1a and 1b in a ratio of about 2:1. 3 predominantly exists in form of the threo,erythro configurated diastereomer 3b by steric reasons.
    Notes: Die Umsetzung von 1,3-Diiod-1,2,3-tri-tert-butyltriphosphan, I(t-BuP)3I, mit Lithiumaluminiumhydrid führt zu 1,2,3-Tri-tert-butyltriphosphan, H(t-BuP)3H (1). 1 reagiert mit n-Butyllithium zu 1,3-Dilithium-1,2,3-tri-tert-butyltriphosphid, Li(t-BuP)3Li (2), das mit Trimethylchlorsilan weiter zu 1,3-Bis(trimethylsilyl)-1,2,3-tri-tert-butyltriphosphan, Me3Si(t-BuP)3SiMe3 (3), umgesetzt werden kann. Die Triphosphane 1, 2 und 3 konnten in reiner Form isoliert werden. In Lösung bildet 1 die threo, threo- und threo,erythro-konfigurierten Diastereomere 1 a und 1 b im Verhältnis von etwa 2:1. 3 liegt aus sterischen Gründen hauptsächlich in Form des threo, erythro-konfigurierten Diastereomers 3 b vor.
    Additional Material: 3 Ill.
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  • 51
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 509 (1984), S. 145-152 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Oxidation Products of Intermetallic Compounds. III. Low Temperature Forms of K2Sn2O3 and Rb2Sn2O3 and a Notice about K2Ge2O3By controlled oxidation of KSn (at 320°C) and RbSn (at 410°C) with O2 the hitherto unknown low temperature forms of K2Sn2O3 (a = 8.4100(8) Å) and Rb2Sn2O3 (a = 8.6368(8) Å) are obtained, which are isotopic with cubic K2Pb2O3. Oxidation at higher temperatures (at 510-5207°C) leads to the well-known HT-forms. The Madelung Part of Lattic Energie, MAPLE, is calculated for both compounds.K2Pb2O3, Rb2Pb2O3, Cs2Pb2O3, and Cs2Sn2O3 have been prepared too by oxidation of KPb, RbPb, CsPb, and CsSn.Oxidation of KGe (at 400°C) leads to the first oxogermanate(II), K2Ge2O3 (cubic a = 8.339(1) Å, isotypic with K2Pb2O3) together with K6Ge2O7.
    Notes: Aus KSn bzw. RbSn entstehen durch direkte Oxydation K2Sn2O3 bzw. Rb2Sn2O3 bei 320°C bzw. 410°C die bislang unbekannten „Tieftemperaturformen“ (a = 8,4100(8)Å bzw. a = 8,6368(8)Å), isotyp mit kubischem K2Pb2O3. Bei höherer Temperatur (510 bzw. 520°C) entstehen die bekannten Hochtemperaturformen.Der Madelunganteil der Gitterenergie, MAPLE, wird berechnet und diskutiert.Ebenso erhält man durch direkte Oxydation von KPb, RbPb, CsPb und CsSn die Oxide K2Pb2O3, Rb2Pb2O3, Cs2Pb2O3 und Cs2Sn2O3. Durch Oxydation von KGe wurde bei 400°C erstmals K2Ge2O3 (kubisch a = 8,339(1) Å; isotyp mit K2Pb2O3) neben K6Ge2O7 erhalten.
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  • 52
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    Zeitschrift für anorganische Chemie 509 (1984), S. 174-182 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Die Reaktion des SnCl2 mit Br2 und I2 in schwachen Donor-LösungsmittelnEs wurden die Verbindungen SnCl2Br2(MeCN)2, “Sn3Cl8Br4(THF)6” und “Sn3Cl10Br2(OEt)6” durch Reaktion zwischen SnCl2 und Br2 in Acetonitril (MeCN), Tetrahydrofuran (THF) und Diethylether (OEt2) gewonnen. Die zwei letzten Verbindungen sind feste Lösungen von SnCl4L2 und SnCl2Br2L2 (L = THF, OEt2) jeweils im Verhältnis 1:2 und 2:1. Die Verbindungen wurden mit Hilfe von IR-, Raman- und Mößbauer-Spektroskopie charakterisiert. Es wurde C1-Symmetrie für SnCl2Br2(MeCN)2 und C2v mit den Liganden in trans-Position für SnCl2Br2L2 (L = THF, OEt2) gefunden. Das bisher nicht bekannte Mößbauer-Spektrum des SnBr4(THF)2 wurde gemessen und ebenfalls die Reaktion zwischen SnCl2 und I2 in denselben Lösungsmitteln studiert. Die Bildung des SnCl4L2 (L = MeCN, THF, OEt2) SnI4 und einer kleinen Menge des SnI3Cl wurde beobachtet und Raman-spektroskopisch identifiziert.
    Notes: The compounds SnCl2Br2(MeCN)2, “Sn3Cl8Br4(THF)6”, and “Sn3Cl10Br2(OEt2)6” were obtained by reaction between SnCl2 and Br2 in acetonitrile (MeCN), tetrahydrofuran (THF) and diethyl ether (OEt2). The two last are solid solutions of SnCl4L2 and SnCl2Br2L2 (L = THF, OEt2) in the proportions 1:2 and 2:1, respectively. The compounds are characterized by IR, Raman, and Mössbauer spectroscopy, a C1 symmetry being found for SnCl2Br2 (MeCN)2 together with a C2v symmetry, with the ligands in trans positions, for SnCl2Br2L2 (L = THF, OEt2). The Mössbauer spectrum of SnBr4(THF)2 was also obtained, which has not previously been reported. The reaction between SnCl2 and I2 has also been studied in the same solvents, and the formation of SnCl4L2 (L = MeCN, THF, OEt2), SnI4, and a small amount of SnI3Cl was observed, which have been identified by Raman spectroscopy.
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  • 53
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    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 509 (1984), S. 192-200 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Einige Cobalt(II)-Komplexe von 4,6-Dimethylpyrimidin-2(1H)-on (HL) wurden dargestellt und mittels IR- und Elektronenspektren magnetochemisch und konduktometrisch untersucht. Der Ligand wird über das nicht protonierte N-Ringatom angelagert und in einem Fall auch über das O-Atom der Carbonylgruppe. Die “blauen” Komplexe [CoX2 · 2HL] (X2 = Cl2, CBr, Br2, (NCS)2) und [CoX2 · 2HL] · 2HL (X = Cl, Br) haben eine verzerrte C2v-Anordnung [CoX2N2]; die Thiocyanate sind über die N-Atome an das Metall gebunden. Die „grünen“ Komplexe CoX2 · 2HL (X = Cl(4H2O), Br) besitzen eine quadratisch-pyramidale Anordnung [CoX2N2O]. Die „rosa“ Komplexe CoX2 · 4HL · nH2O (X = ClO4, n = 2, X = BF4, n = 8, CF3CO2, n = 4) und die „cremefarbigen“ CoX2 · 4HL · 6H2O (X = J, ClO4) zeigen oktaedrische Anordnung; nur CF3CO2- ist koordiniert. Die „veilchenfarbenen“ Komplexe CoAcL · 2HL · 2H2O und Co3Ac4L2 · 2HL · 2H2O haben eine mehrkernige Struktur; das Acetation betätigt sich als zweizähniger Ligand.
    Abstract: CoII-Komplexe von 4,6-Dimethylpyrimidin-2(1H)-on
    Notes: Some cobalt(II) complexes of 4,6-dimethylpyrimidine-2(1H)-one (HL) have been prepared and studied by infrared and electronic spectra and by magneto-chemical and conductometric measurements. The ligand is coordinated through the unprotonated ring-nitrogen atom and in one case also through the carbonylic oxygen atom. The “blue” complexes [CoX2 · 2HL] (X2 = Cl2, ClBr, Br2, (NCS)2) and [CoX2 · 2HL] · 2HL (X = Cl, Br) have a distorted C2v [CoX2N2] coordination; the thiocyanate ion is N-bonded to the metal. The “green” complexes CoX2 · 2HL (X = Cl(4H2O), Br) have a square-pyramidal [CoX2N2O] coordination. The “pink” CoX2 · 4HL · nH2O (X = ClO4, n = 2; X = BF4, n = 8; X = F3Ac, n = 4) and “cream” CoX2 · 4HL · 6 H2O (X = I, ClO4) complexes have an octahedral coordination; only the F3Ac- ion is coordinated. The “cyclamen” CoAcL · 2HL · 2 H2O and Co3Ac4L2 · 2HL · 2H2O complexes have a polynuclear constitution; the Ac- ion behaves as bidentate ligand.
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  • 54
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    Zeitschrift für anorganische Chemie 510 (1984), S. 31-36 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Raman Spectroscopic Investigations of Coordination Polymeric Metal TricyanmethanidesThe Raman spectra of 3d-metal tricyanmethanides M{C(CN)3}2 as well as of [Ni{C(CN)3}2py2] are investigated. The observed Raman lines are assigned, characteristic variations of position and intensity of these lines are discussed.
    Notes: Es werden die Ramanspektren der koordinationspolymeren 3d-Metalltricyanmethanide M{C(CN)3}2 (M = Mn, Fe, Co, Ni, Zn) sowie von [Ni{C(CN)3}2py2] untersucht. Die beobachteten Ramanlinien werden zugeordnet, charakteristische Variationen der Lage und Intensität dieser Linien werden diskutiert.
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  • 55
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    Zeitschrift für anorganische Chemie 510 (1984), S. 51-60 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemistry and Structural Chemistry of Phosphides and Polyphosphides. 34. Vapor Pressure Measurements in the Europium-Phosphorus SystemThe vapor pressure of the europium phosphides EuP7, α-EuP3, ß-EuP3, EuP2 and Eu3P4 were measured using the Knudsen-Effusion technique. These compounds were vaporized incongruently according to the general reaction a EuPm, (s) = a EuPn, (s) + P4, (g) where a (m - n) = 4. The following enthalpies and entropies of reaction were calculated (δH)kJ · mol-1/δS (J · K-1 mol-1)/ T(K). [δH/δS/T]: EuP7 → ß-EuP3 [191/215/698]; α-EuP3 → EuP2 [212/162/847]; ß-EuP3 → EuP2 [261/212/847]; EuP2 → Eu3P4 [209/144/868]; Eu3P4 → EuP [240/131/1110]. The temperature and pressure ranges over which these phosphides exist were determined from the above values. Standard enthalpies of formation relative to EuP(s) were calculated by combining different reaction enthalpies. The results demonstrate the relatively high stability of ß-EuP3, EuP7 and the instability of EuP2.
    Notes: Für die Europiumphosphide EuP7, α-EuP3, ß-EuP3, EuP2 und Eu3P4 wurden die Dampfdrucke der inkongruenten Verdampfungsreaktionen a EuPm, (f) = a EuPn, (f) + P4, (g) mit a(m - n) = 4 mit der Knudsen-Methode gemessen. Zur Abspaltung von einem Mol P4,(g) wurden bei den mittleren Temperaturen T(K) die folgenden Reaktionsenthalpien δH(kJ · mol-1) und Reaktionsentropien δS(J · K-1 · mol-1) erhalten: [δH/δS/T]: EuP7 β ß-EuP3 [191/215/698]; α-EuP3 → EuP2 [212/162/847]; ß-EuP3 → EuP2 [261/212/847]; EuP2 → Eu3P4 (209/144/868); Eu3P4 → EuP [240/131/1110]. Hierdurch wurden die Existenzfelder der verschiedenen Europiumphosphide in Abhängigkeit von Druck und Temperatur festgelegt. Durch Kombination der verschiedenen Reaktionsenthalpien werden die Standardbildungsenthalpien der Phosphide relativ zu EuP berechnet. Sie zeigen die hohe Stabilität von ß-EuP3 und EuP7 sowie die Instabilität von EuP2.
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  • 56
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    Zeitschrift für anorganische Chemie 508 (1984), S. 86-92 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of (PPh4)2[Mo2Cl10]The title compound is obtained in the reaction of [MoCl4(Ph—C≡C—Ph)]2 with tetraphenylphosphonium chloride in dichloro methane, forming brown crystals. It is characterized by the i.r. spectrum and a crystal structure analysis by the aid of X-ray diffraction data. The complex crystallizes triclinic in the space group P1 with one formula unit per unit cell. The cell dimensions are a = 1122 pm, b = 1137 pm, c = 1283 pm; α = 63.4°, β = 69.1°, γ = 86.5°. The crystal structure determination (2959 observed, independent reflexions, R = 4.5%) shows the constants of the unit cell to consist of on centrosymmetric anion, two cations and one disordered molecule of dichloro methane. The distance Mo—Mo in the anion is 380 pm, which excludes direct magnetic interaction between the molybdenum atoms.
    Notes: Die Titelverbindung entsteht in Form brauner Kristalle durch Umsetzung von [MoCl4(Ph—C≡C—Ph)]2 mit Tetraphenylphosphoniumchlorid in Dichlormethan; sie wird durch das IR-Spektrum und durch eine Kristallstrukturbestimmung charakterisiert. Der Komplex kristallisiert triklin in der Raumgruppe P1 mit einer Formeleinheit pro Elementarzelle. Die Zellparameter betragen a = 1122 pm, b = 1137 pm, c = 1283 pm, α = 63,4°, β = 69,1°, γ = 86,5°. Die röntgenographische Kristallstrukturbestimmung (2959 beobachtete, unabhängige Reflexe, R = 4,5%) zeigt, daß die Struktur aus zentrosymmetrischen, dimeren Anionen, isolierten Kationen, und einem fehlgeordneten Molekül Dichlormethan pro Elementarzelle besteht. Der Mo—Mo-Abstand im Anion beträgt 380 pm, was eine direkte magnetische Wechselwirkung zwischen den Mo-Atomen ausschließt.
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  • 57
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Crystal and Molecular Structure of Tris(diethyldithiocarbamato)dimethylphenylphosphinetechnetium (III)The title compound Tc(S2CNEt2)3(Me2PhP) I has been prepared by the reaction of TcCl3(Me2PhP)3 with NaS2CNEt2. The crystal structure of I has been determined by single-crystal X-ray diffraction methods at room temperature. Crystals are rhombic, space group P212121, with a = 8.708(1), b = 12.012(1), c = 29.626(3) Å and Z = 4. The compound consists of discrete I molecules. The technetium atom has a seven-coordinated environment which is best described as a distorted pentagonal bipyramid. The Tc - P distance (2.330(3) Å) is remarkably short compared with other technetium complexes with mono-dentate phosphine ligands.
    Notes: Die Titelverbindung Tc(S2CNEt2)3(Me2PhP) I wurde durch Reaktion von TcCl3(Me2PhP)3 mit NaS2CNEt2 dargestellt und ihre Kristall- und Molekülstruktur durch Röntgenstrukturanalyse ermittelt. Die Kristalle sind rhombisch, Raumgruppe P212121, mit a = 8,708(1), b = 12,012(1), c = 29,626(3) Å und Z = 4. Die Verbindung besteht aus diskreten monomeren Molekülen. Das Technetiumatom hat siebenfache Koordination, die am besten als geringfügig verzerrte pentagonale Bipyramide beschrieben werden kann. Die Tc - P-Bindungslänge (2,330(3) Å) ist bemerkenswert kurz im Vergleich zu anderen Technetiumkomplexverbindungen mit einzähnigen Phosphanen.
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    Zeitschrift für anorganische Chemie 510 (1984), S. 152-162 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermodynamics and Structure of Molten Mixtures Alkali Halide-Alkaline Earth HalideThermodynamic quantities ai, fi, GE, and SE were calculated on the basis of vapour pressures of molten mixtures of the type alkali halide-alkaline earth halide. Negative deviations from ideality were found in all systems. The influence of cations or anions on the properties of mixtures is discussed. There is a good correlation between GE and the change of polarization energy δEp. Strong ionic interactions were found in molten mixtures, especially in the system RbBr - CaBr2. The existence of stable complex ions in melts could not be shown by Raman spectroscopy.
    Notes: Aus den Dampfdrücken der geschmolzenen Mischungen vom Typ Alkalimetallhalogenid-Erdalkalimetallhalogenid wurden die thermodynamischen Daten ai, fi, GE sowie Orientierungswerte für SE berechnet. In allen Systemen treten z. T. beträchtliche negative Abweichungen von der Idealität auf. An ausgewählten Beispielen wird der Einfluß der Kationen bzw. Anionen auf die Mischungseigenschaften diskutiert. Für die GE-Werte ergibt sich eine gute Korrelation mit der Änderung der Polarisationsenergie δEp. Ramanspektroskopische Untersuchungen konnten die Existenz stabiler komplexer Ionen nicht belegen, weisen aber besonders bei den Mischungen RbBr - CaBr2 auf starke interionische Wechselwirkungen hin.
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  • 59
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    Zeitschrift für anorganische Chemie 510 (1984), S. 189-193 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Die binären und ternären Gleichgewichte im System MoO3 - TeO2 - Al2O3 wurden rötgenographisch untersucht. Bei 750°C in Luft wurden in diesem System die im Abstract angegebenen koexistierenden Bereiche gefunden. Eine Bildung ternärer Verbindungen konnten im untersuchten Temperaturbereich (450 - 750°C) nicht beobachtet werden.
    Notes: The binary and ternary equilibrium reactions of Al2O3 with TeO2 and MoO3 were studied by X-ray diffraction methods and the following compatibility ranges were determined in the TeO2 - MoO3 - Al2O3 system at 750°C in air: TeO2, Te2MoO7, Al2TeO6; Te2MoO7, MoO3, Al2TeO6; MoO3, Al2(MoO4)3, Al2TeO6; Al2(MoO4)3, Al2O3, Al2TeO6. Ternary compound formation was not observed in the temperature range investigated (450 - 750°C).Phasengleichgewichte im System MoO3 - TeO2 - Al2O3.
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  • 60
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N.M.R. Spectroscopic Studies of 15N Labelled N-Phosphorylphosphazenes and Imidodiphosphoric Acid Derivatives15N labelled compounds were prepared and investigated by means of 31P- and 15N-NMR spectroscopy. The chemical shift values δP and δN, and the coupling constants 1JPN and 2JPP are discussed and interpreted qualitatively by semiempirical quantumchemical calculations (CNDO/2) using POPLE'S ΔE-model.
    Notes: 15N-markierte Verbindungen der Substitutionsreihen wurden synthetisiert und mit Hilfe der 31P- und 15N-NMR-Spektroskopie untersucht. Die chemischen Verschiebungen δP und δN sowie die Kopplungskonstanten 1JPN und 2JPP werden diskutiert und qualitativ mit Hilfe halbempirischer quantenchemischer Rechnungen (CNDO/2) im Rahmen des POPLE-schen ΔE-Modells interpretiert.
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  • 61
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of the Two-component System Triethylphosphite/Carbon Tetrachloride with Nucleophiles Containing Hydrogen. 1. Reaction with Acyl AmidesAcyl amides react with the two-component system triethylphosphite/carbon tetrachloride yielding N-acyl phosphazenes, (EtO)3P=N—Ac. In this way (EtO)3P=N—P(O)(OEt)2, (EtO)3P=N—CN, (EtO)3P=N—C(O)Ph, and (EtO)3P=N—SO2Ph were prepared. Ethyl esters of phosphoric acid and trichloromethane phosphonic acid were obtained as by-products.
    Notes: Säureamide reagieren mit dem Zweikomponentensystem Triethylphosphat/Tetrachlorkohlenstoff zu N-Acylphosphazenen, (EtO)3P=N—Ac. Auf diese Weise wurden aus entsprechenden Amiden (EtO)3P=N—P(O)(OEt)2, (EtO)3P=N—CN, (EtO)3P=N—C(O)Ph und (EtO)3P=N—SO2Ph dargestellt. Als Nebenprodukte werden Phosphorsäureethylester und Trichlormethanphosphonsäureester erhalten.
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  • 62
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Discrete Polynuclear Metal Complexes from Polysulfide Solutions: [Cu6S17]2-, a Novel Binary Polynuclear CuI Complex with Several Remarkable Structural FeaturesThe complex [Cu6S17]2-, obtained from Cu(acac)2 and an ethanolic polysulfide solution, contains an unusual arrangement of the metal atoms and novel types of ligand coordination, particularly of polysulfido (S42- and S52-) ions. The relevance of the synthesis with respect to the “dilemma of transporting metals together with sulfur” for the process of metal sulfide rock formation is evidenced. (PPh4)2[Cu6S17] crystallizes in the space group C2/c with Z = 4 (for further details see Inhaltsübersicht).
    Notes: Der Komplex [Cu6S17]2-, der als Tetraphenylphosphonium-Salz (1) aus Cu(acac)2 und einer ethanolischen Polysulfidlösung erhalten wurde, zeigt eine ungewöhnliche Anordnung der Metall-Atome und eine neuartige Koordination von Polysulfidoliganden (S42- und S52-). Auf die Relevanz der Synthese bezüglich der Problematik der Entstehung von Metall-Sulfid-Mineralien wird hingewiesen. 1 kristallisiert monoklin in der Raumgruppe C2/c mit Z = 4 (Gitterdimensionen a = 20,270(7), b = 11,605(5), c = 26,331(9) Å, β = 109,68(4)°).
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    Zeitschrift für anorganische Chemie 511 (1984), S. 108-131 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Organosilicon Compounds. 97. About the Influence of the Si-Substituents (Me, Cl) upon the Formation and the Reactions of Ylides1,3-disilapropanes with different grade of chlorination or methylation at the silicon atoms and containing a CCl2 group cleave the Si—P bond of Me3SiPMe2. By subsequent rearrangement ylides with = PMe2Cl group are formed. The reactivity of the CCl2 group depends on the grade of Si-chlorination resp. Si-methylation. Si-methylation decreases the reactivity of the CCl2 group. The reaction of 1,3-disilapropanes and Me3SiPMe2 (molar ratio 1:1) runs in a sequence shown in “Inhaltsübersicht”. Ylid C is able either to react with the initial compound A forming B, or in competition decomposes forming D. Reacting Si-perchlorinated carbosilanes, the decomposition forming D is not to be observed. In Si-methylated ylides like (Me3Si)2C=PMe2—PMe2 and (Me3Si)2C=PMe2—P(Me)SiMe3 the ylid carbon atom is able to abstract a proton of the P—CH3 group resp. P—H groups of the trivalent phosphorus forming (Me3Si)2C(H)PMe2. The rearrangement is proved by deuterated derivatives. The different behaviour is due to the increased basicity of the ylid-C atom in Si-methylated phosphorus ylides. Quite the same behaviour show the phosphorus ylides of 1,3,5-trisilacyclohexane.
    Notes: Die am Si-Atom unterschiedlich chlorierten und methylierten 1,3-Disilapropane mit der CCl2-Gruppe ermöglichen die Spaltung von Me3Si—PMe2 unter Bildung der P-halogenierten Phosphorylide, wobei mit steigendem Methylierungsgrad die Reaktivität abnimmt. Die Umsetzungen verlaufen in folgender Reaktionsfolge: Das Ylid C kann mit der nicht umgesetzten Ausgangsverbindung A zu B zurückreagieren oder es zersetzt sich in einer Konkurrenzreaktion zu D. Bei Si-chlorierten Yliden wird die Bildung von D nicht beobachtet. In Si-methylierten Yliden wie (Me3Si)2C=PMe2—PMe2 und (Me3Si)2C=PMe2—P(Me)SiMe3 vermag das Ylid-C-Atom ein H-Atom aus der P—CH3-Gruppe oder der PH-Gruppe des dreibindigen Phosphors zu abstrahieren unter Bildung von (Me3Si)2C(H)PMe2. Die Umlagerung wird anhand deuterierter Derivate belegt. Das unterschiedliche Verhalten wird auf die erhöhte Basizität des Ylid-C-Atoms in den Si-methylierten Phosphoryliden zurückgeführt. Ganz entsprechend verhalten sich die Phosphorylide 1,3,5-Trisilacyclohexans.
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    Zeitschrift für anorganische Chemie 511 (1984), S. 176-184 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polymorphism of SrTa2O6Orthorhombic SrTa2O6 is a new low temperature modification related to orthorhombic CaTa2O6. SrTa2O6(orh.) was obtained when the wellknown modification SrTa2O6(TTB) which is related to the tetragonal tungsten bronzes was heated in the presence of a transporting agent (chlorine) or a mineralizer (melt of B2O3) at temperatures below 1150°C. It could be prepared by the reaction of a 1:1 mixture of Sr(NO3)2 or SrCO3 with Ta2O5 in a sealed quartz glass tube as well. SrTa2O6(orh.) also occurred as an intermediate phase of the reaction of the corresponding 1:2 mixture at temperatures below 900°C (e. g. 840°C). Indexing of Guinier powder patterns led to the following unit cell: a = 11.006 Å, b = 7.638 Å, c = 5.622 Å. At temperatures above 1220°C SrTa2O6(orh.) changes (in air) to SrTa2O6(TTB). A reversal of this transition could not be achieved without the presence of a mineralizer or a transporting agent. CaxSr1-xTa2O6 solid solutions of the low temperature form could not definitely be established. However, at 1300°C solid TTB solutions of CaxSr1-xTa2O6 were formed. For x 〉 0.05 the TTB unit cells are orthorhombically distorted. For x ≥ 0.85 the x-ray powder patterns of the solid solutions looked like the one of CaTa2O6(orh.) and no TTB-structure was observed at 1300°C.
    Notes: Von SrTa2O6 wurde eine neue, mit orthorhombischem CaTa2O6 strukturverwandte Tieftemperatur-Modifikation erhalten. SrTa2O6(orh.) ließ sich bei Temperaturen unter 1150°C sowohl aus der bisher bekannten, den tetragonalen Wolframbronzen verwandten Modifikation SrTa2O6(TWB) in Gegenwart eines Transportmittels (Chlor) bzw. eines Mineralisators (B2O3-Schmelze), wie auch durch Umsetzen von Gemengen (1:1) aus SrCO3 oder Sr(NO3)2 und Ta2O5 in geschlossenen Quarzglasampullen erhalten. Auch als Zwischenprodukt der Umsetzung entsprechender 1:2-Gemenge bei Temperaturen unter 900°C (z. B. 840°C) tritt diese Modifikation auf. Die Gitterkonstanten von SrTa2O6(orh.) sind aufgrund von Pulverdaten: a = 11,006 Å, b = 7,638 Å, c = 5,622 Å. Beim Erhitzen auf etwa 1 220°C (an der Luft) wandelt sich SrTa2O6(orh.) in SrTa2O6(TWB) um. Eine Rückumwandlung von SrTa2O6(TWB) in SrTa2O6(orh.) ohne Mineralisator- oder Transportmittelzusatz war nicht zu erreichen. Mischkristalle CaxSr1-xTa2O6 der Tieftemperaturform ließen sich nicht sicher nachweisen. Die bei Mischkristallen mit 0,05 〈 x ≤ 0,20 (1300°C) vorliegende TWB-Struktur ist orthorhombisch verzerrt. CaTa2O6(orh.) zeigte dagegen ab x ≥ 0,85 (1300°C) keine Entmischung.
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  • 65
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    Zeitschrift für anorganische Chemie 509 (1984), S. 167-173 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation, Isolation, and Characterization of Mixed Thiocyanato(1.3-diaminopropane) -chromium(III) ComplexesThe complexes [Cr(NCS)4dap]- and trans-[Cr(NCS)2(dap)2]+ (dap = 1.3-diaminopropane) are prepared for the first time, isolated as salts and characterized by CHN analysis, chromium contents, the electrophoretic behaviour in dimethylformamide, and by UV, VIS, and IR spectra.
    Notes: Die Komplexe [Cr(NCS)4dap]- und trans-[Cr(NCS)2(dap)2]+ (dap = 1,3-Diaminopropan) werden erstmals dargestellt, als Salze isoliert und durch CHN-Analyse, Chrombestimmung, elektrophoretisches Verhalten in Dimethylformamid sowie Spektren im UV, VIS und IR charakterisiert.
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  • 66
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    Zeitschrift für anorganische Chemie 509 (1984), S. 201-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Schwefel-Stickstoff-Chelatbildner. IV. Einige Kupfer(II)-Komplexe von Thioaminopyridinen. IR- und ReflexionsspektroskopieEine Reihe von CuII-Komplexen sind dargestellt und charakterisiert worden. Die angenommenen Strukturen beruhen auf ihren IR -und VIS-Spektren. Die Thioaminopyridine können in verschiedener Weise koordiniert sein. Im Gegensatz zu unseren Befunden an aliphatischen Thioaminen ergab sich kein Zusammenhang zwischen der Struktur der CuLX2-Verbindungen und der Art des X--Anions. Ein Hinweis auf die Struktur der CuL2+-Komplexe in wäßriger Lösung kann aus festem CuLX2 nicht erhalten werden.
    Notes: A series of solid state CuII complexes with thia-aminopyridines . S(CH2)mNH2 have been prepared and characterized. The postulated structures of these CuLX2 (X = OAc-, NO3-, ClO4- or Cl-) compounds were based on their I.R. and electronic spectra. It was found that the thiaaminopyridines may coordinate in quite different ways. In contrast with what was found for the aliphatic thiadiamines, no relation was stated between the structure of the CuLX2 compounds and the nature of the X- anion.Moreover the solid state compounds do not give a clear indication for the structure of the CuL2+ species in aqueous solution.
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  • 67
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    Zeitschrift für anorganische Chemie 510 (1984), S. 199-207 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermochemische Eigenschaften und Aufwachsen von Hg1-xCdxTe auf CdTeNach thermodynamischen Rechnungen enthält die Gasphase des epitaktischen Hg1-xCdxTe - HgI2 - CdTe Systems vorwiegend Hg(g) und HgI2(g) durch die andere Moleküle vom Ausgangsstoff zum CdTe Substrat wandern. Transportversuche im Temperaturgradienten 590° → 535°C zeigten, daß man dünne Schichten von Hg1-xCdxTe auf CdTe von einem ternären Ausgangsmaterial in Gegenwart von HgI2 erhält.
    Notes: Based on a thermodynamic analysis, the vapor phase of the Hg1-xCdxTe - HgI2 - CdTe epitaxy system consists predominantly of Hg(g) and HgI2(g) through which nutrient species migrate from the source to the CdTe substrate. Growth experiments in the 590° → 535°C temperature gradient showed that Hg1-xCdxTe layers can be grown on CdTe substrates using a preannealed, ternary source material in the presence of HgI2.
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  • 68
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical Transport Reactions of Ni-Sulfides and Some Relationships in C.T.R. of Complex Solids in the Case of Sulfides of Fe, Co, NiCrystals of α-Ni3S2, NiS, and NiS2 as well as solid solutions Fe1-yNiySx were grown by C.T.R. The coexistence equilibrium pressure of the solution equilibrium pressure p(S2), the activity of the metal component, the stability of gaseous metal halides concerning decomposition as well as their stability related on the transport agent have to be taken into account to choose a suitable transport agent, which have a sometimes opposite influence on the transport behaviour. Halogenes, hydrogen halides, and GeI2 were used as transport medium.
    Notes: Durch chemische Transportreaktionen wurden Kristalle der Phasen α-Ni3S2, NiS und NiS2 sowie Mischkristalle Fe1-yNiySx erhalten. Bei der Auswahl des Transportmittels sind der Koexistenzzersetzungsdruck bzw. Löslichkeitsdruck p(S2) und die Metallaktivität im Bodenkörper, die Stabilität der gasförmigen Metallhalogenide bezüglich Zerfall und ihre Stabilität relativ zum Transportmittel zu beachten, die z. T. gegenläufigen Einfluß haben. Geeignete Transportmittel sind Halogene, Halogenwasserstoffe und GeI2.
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  • 69
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    Zeitschrift für anorganische Chemie 511 (1984), S. 57-71 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical Transport of Zinc Oxide and the Estimation of its Phase WidthThe chemical transport behaviour of zinc oxide using different transport agents and the influence of the transport conditions (T, ΔT, p) on transport rate and deposition form was studied. The range of homogeneity of ZnO is very narrow. The best agents for deposition of ZnO with the upper phase boundary are Cl2 and Br2, for the deposition of the lower phase boundary HBr and NH4Br are more suitable. The deviation from stoichiometry depends on the deposition temperature and amounts to 10 till 250 ppm in the range of 1073 up to 1373 K.
    Notes: Das chemische Transportverhalten von Zinkoxid mit Cl2, Br2, HCl, HBr, NH4Cl und NH4Br und der Einfluß der Transportbedingungen (T, ΔT, p) auf die Abscheidungsgeschwindigkeit und Abscheidungsform wurde studiert. ZnO weist ein sehr schmales Homogenitätsgebiet auf. Zur Abscheidung von ZnO der oberen Phasengrenzzusammensetzung sind Cl2 und Br2 am besten geeignet. Für die Abscheidung von ZnO der unteren Phasengrenzzusammensetzung sind am besten HBr und NH4Br geeignet. Die Abweichung von der Stöchiometrie hängt von der Präparationstemperatur der Kristalle ab und liegt zwischen 10 und 250 ppm im Temperaturbereich 1073 bis 1373 K.
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  • 70
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    Zeitschrift für anorganische Chemie 511 (1984), S. 89-94 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXVIII. Reactions of Dibenzyl Manganese with Oxygene(C6H5CH2)2Mn · C4H8O2 reacts with oxygen forming an unstable deep violet compound which changes in a stable unsoluble yellow peroxide of the formula C6H5CH2MnO—OMnCH2C6 H5. With excess oxygen a polynuclear complex of 3 valent manganese is formed with the composition Mn4O4(OH)4(OCHC6H5)2.The compounds isolated were characterized by the products of hydrolyses and thermolyses, anaerobic reaction with iodine, magnetic moments, i.r. and e.s.r. spectra.
    Notes: Dibenzylmangan-1,4-dioxan reagiert mit Sauerstoff zu einer tiefvioletten instabilen Substanz. Diese wandelt sich in ein stabiles gelbes, schwerlösliches Peroxid der Formel C6H5CH2MnO—OMnCH2C6H5 um. Mit überschüssigem Sauerstoff entsteht daraus ein Mehrkernkomplex des 3wertigen Mangans der Zusammensetzung Mn4O4(OH)4(OCHC6H5)2.Die isolierten Verbindungen wurden durch ihre Hydrolyse- und Thermolyseprodukte, anaerobe Iodierung, magnetischen Momente sowie IR- und ESR-Spektren näher charakterisiert.
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  • 71
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    Zeitschrift für anorganische Chemie 508 (1984) 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 72
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    Zeitschrift für anorganische Chemie 508 (1984), S. 19-25 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Structure of Antimony (III) Tris (thiophosphinates)The title compounds are formed by the reaction of Sb(CH3COO)3 with thiophosphinic acids R2P(=S)OH (R = CH3 cyclo-C6H11, C6H5). The crystal and molecular structures of Sb((cyclo-C6H11)2POS)3 and Sb((C6H5)2POS)3 have been determined by single crystal X-ray methods. SbIII is pyramidally coordinated to the oxygen atoms of the R2POS ligands through short (primary) bonds with a mean length of 203 pm. The Sb—S distances of the mainly chelating ligands vary between 300 and 320 pm (secondary bonds). The lone electron pair is stereochemically active.
    Notes: Die Umsetzung von Sb(CH3COO)3 mit Thiophosphinsäuren R2P(=S)OH (R = CH3, cyclo-C6H11, C6H5) führt zu Verbindungen der Formel Sb(R2POS)3. Die Strukturen der Verbindungen mit R = cyclo-C6H11 und C6H5 wurden an Einkristallen röntgenographisch bestimmt. SbIII ist über kurze (primäre) Bindungen mit der mittleren Länge von 203 pm pyramidal an die Sauerstoffatome der R2POS-Liganden gebunden. Die Sb—S-Abstände (sekundäre Bindungen) sind ungefähr 320 pm lang. Das freie Elektronenpaar ist stereochemisch aktiv.
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    Zeitschrift für anorganische Chemie 508 (1984), S. 43-49 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: I.R. and Mass Spectroscopic Investigations on α,ω-Dihydrochloro Silanes H(SiCl2)nH with n = 3-7Mass spectra of α,ω-dihydrochlorosilanes H(SiCl2)nH were analyzed respecting to their fragmentation. This shows, that the cleavage starts with the break of SiSi bonds, by preference in the middle of the chain. This is in accordance to the results of IR spectra which show very similar frequencies like perchlorooligo silanes. Thus, the lowest force constants of SiSi bondings in α,ω-dihydrochloro silanes, can be also expected in the middle of the chain.
    Notes: Die Massenspektren der α,ω-Dihydrochlorsilane H(SiCl2)nH mit n = 3-7 werden bezüglich ihrer Fragmentierung analysiert. Es zeigt sich, daß die Spaltung mit einem Zerbrechen der SiSi-Bindung, vorzugsweise in der Mitte der Kette beginnt. Dies steht im Einklang mit den Ergebnissen der IR-Spektren, die sehr ähnliche Frequenzen zeigen, wie bei den Perchlorsilanen gefunden. Daraus kann geschlossen werden, daß auch bei den α,ω-Dihydrochlorsilanen die mittleren SiSi-Bindungen die kleinsten Kraftkonstanten zeigen.
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  • 74
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phase Determinations by X-rays on the Thermal Dissociation and the Hydrolysis of Alkali Hexafluorogermanates at Higher TemperaturesFor a better understanding of the thermal dissociation of alcaline hexafluorosilicates investigations have been done on hexafluorogermanates. In these systems the formation of new phases has been studied by x-rays in dependence of temperature. Thermal behaviour of the substances strongly depends on the starting structure. Phase transformations taking place at lower temperatures are strongly determine the reaction at higher temperature. Therefore, we found differences to the analogous thermal reactions of hexafluorosilicates.There is a high sensitivity to hydrolysis of hexafluorogermanates above 600°C. We discuss the difference in reaction of thin powder layers and of powder samples in the volume.
    Notes: Zum besseren Verständnis des thermischen Verhaltens von Alkalihexafluorosilicaten wurden Vergleiche mit analogen Germanium-Verbindungen angestellt. Die Phasenneubildung wurde als Funktion der Temperatur röntgenographisch untersucht. Es ergab sich eine starke Abhängigkeit des thermischen Verhaltens von der Ausgangsstruktur. Phasentransformationen, die bei niederen Temperaturen ablaufen, beeinflussen bei höherer Temperatur das Reaktionsgeschehen (thermische Vorgeschichte der Substanz). Deshalb resultieren gegenüber den Hexafluorosilicaten differierende Reaktionsabläufe. Durch Heizguinieraufnahmen unter getrocknetem, strömendem Inertgas wurde die enorme Hydrolysenempfindlichkeit der Hexafluorogermanate oberhalb 600°C bewiesen.Das unterschiedliche Verhalten von dünnen Pulverschichten und kompakten Pulverproben wird diskutiert.
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  • 75
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Organosilicon Compounds. 99. Separation of Carbosilane and Silylphosphane Mixtures by Means of HPLCTest mixtures of Si-methylated carbosilanes were separated by means of reversedphase HPLC (nucleosil 5-C18; CH3OH:hexane = 90:10). The corresponding SiCl-containing mixtures were successfully separated only after reductin of the SiCl groups by means of LiAlH4 (CH3OH: C6H6 + H2O = 92.5:7.5 + 4 - 8%). A model separation of the silylphosphanes Me3SiPH2, (Me3Si)2PH and (Me3Si)3P using the same material but acetonitrile: toluene = 85:15 is also reported.
    Notes: Testgemische Si-methylierter Carbosilane werden mit reversed-phase HPLC getrennt (Nucleosil 5-C18; CH3OH:Hexan = 90:10). Die Auftrennung entsprechender SiCl-haltiger Verbindungen gelingt nach Reduktion der SiCl-Gruppen mit LiAlH4 (CH3OH: C6H6 + H2O = 92,5: 7,5 + 4 - 8%). Über die Modelltrennung der Silylphosphane Me3SiPH2, ((Me3Si)2)2PH und (Me3Si)3P unter Verwendung des gleichen Säulenmaterials, jedoch mit dem Eluens Acetonitril: Toluol = 85:15, wird ebenfalls berichtet.
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    Zeitschrift für anorganische Chemie 512 (1984), S. 177-180 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactivity of Intramolecular Basestabilized Tin(II) Compounds with Halogens, Tin Tetrachloride, and TrichloromethaneIntramolecular basestabilized tin(II) compounds of the type RN(CH2CH2Y)2Sn (Y = O, S and R = Me, t-Bu) react with halogens, tin tetrachloride, and trichloromethan at room temperature by oxydative addition reaction to tin(IV) derivatives. These compounds are characterized by n.m.r. investigations and by Mössbauer studies.
    Notes: Intramolekular basenstabilisierte Zinn(II)-Verbindungen des Typs RN(CH2CH2Y)2Sn (Y = O, S und R = Me, t-Bu) reagieren bei Raumtemperatur mit Halogenen, Zinntetrachlorid und Chloroform im Sinne von oxydativen Additionsreaktionen zu Zinn(IV)-Derivaten. Diese Derivate werden durch NMR-Untersuchungen und durch Mößbauerstudien charakterisiert.
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    Zeitschrift für anorganische Chemie 512 (1984), S. 231-239 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Chalcogenolates. 137. Alkyl Esters of Isothiocyanoformic, Isothiocyanomonothioformic and Isothiocyanodithioformic AcidsThe esters RO—CO—NCS, where R = CH3, C2H5, as well as RS—CO—NCS and RS—CS—NCS with R = C2H5, nC3H7 have been prepared by three different methods. The reaction between the corresponding chloro compound and KSCN in the presence of the phase transfer catalyst 18-crown-6 gives the highest yields.The electron absorption, infrared, nuclear magnetic resonance, and mass spectra of these compounds are reported.
    Notes: Die Ester RO—CO—NCS mit R = CH3, C2H5 sowie RS—CO—NCS und RS—CS—NCS mit R = C2H5, nC3H7 wurden nach drei verschiedenen Verfahren hergestellt, wobei die Umsetzung der entsprechenden Chloroverbindung mit KSCN in Gegenwart des Phasentransferkatalysators 18-Krone-6 die besten Ausbeuten erbringt.Die Elektronenabsorptions-, Infrarot-, kernmagnetische Resonanz- und Massenspektren der Verbindungen werden mitgeteilt.
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    Zeitschrift für anorganische Chemie 508 (1984), S. 191-196 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Coordination and Extraction of Molybdenum(VI) with Bidentate LigandsA series of bidentate ligands as well as their thio derivatives from the groups of 8-quinolinols, β-diketones, acylpyrazolones, and N-acyl-phenylhydroxylamines was studied for the ability to extract molybdenum(VI) from heptamolybdate. The extraction principally runs only in acidic medium, sulfur-containing extractants having no advantage. The composition of the complexes was determined by the isolation of compounds in the solid state and also by the interpretation of distribution data.
    Notes: Eine Reihe zweizähniger Liganden sowie entsprechende Thioderivate aus den Gruppen der 8-Hydroxychinoline, β-Diketone, Acylpyrazolone und N-Acyl-phenylhydroxylamine wurde auf ihr Extraktionsvermögen für Molybdän aus Heptamolybdat geprüft. Die Extraktion ist grundsätzlich nur im sauren Bereich möglich, schwefelhaltige Extraktionsmittel bringen keine Vorteile. Die Komplexzusammensetzung wurde durch Isolierung von Komplexen in Substanz und durch Auswertung der Verteilungsdaten ermittelt.
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    Zeitschrift für anorganische Chemie 508 (1984), S. 201-207 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XXIX. 29Si-N.M.R. InvestigationsThree series of silicon-sulphur compounds (RO)3SiSR′ (I), (i-PrO)4-nSi(SEt)n (II) and cyclic Si—S compounds (III) were prepared, some of them at the first time and their 29Si-N.M.R. spectra were measured. In the series of trialkoxysilylthio derivatives (I) were the steric and inductive effects of the RO and R'S groups evaluated. In the series II were the 29Si-N.M.R. chemical shifts related to the relative paramagnetic screening constants σ* and netto charge at the silicon atom q(Si) using the EN-quantum-chemical model discussed. In the series III were the shift contribution of the (SiS)2 and 1-sila-2,5-dithiacyclopentan rings determined.
    Notes: Drei Reihen von Silicium-Schwefel-Verbindungen: (RO)3SiSR'(I), (i-PrO)4-nSi(SEt)n (II) und cyclische Si—S-Verbindungen (III) wurden dargestellt, davon einige erstmalig, und ihre 29Si-NMR-Spektren vermessen. In der Reihe der Trialkoxysilylthio-Derivate (I) wurden die sterischen und induktiven Wirkungen der RO- und R'S-Gruppen abgeschätzt. In der Reihe II wurden die 29Si-NMR-chemischen Verschiebungen in Abhängigkeit von den relativen paramagnetischen Abschirmungskonstanten σ* und der Nettoladung am Silicium q(Si) im Rahmen des EN-quantenchemischen Modells diskutiert. In der Reihe III wurden die Beiträge des (SiS)2-und 1-sila-2,5-dithia-cyclopentan-Rings zur chemischen Verschiebung ermittelt.
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    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Chalcogenolates. 134. Studies on Esters of Haloformic Acids 2. Synthesis and Properties of Se-Alkyl Esters of Chloromonothiomonoselenoformic AcidThe hitherto unknown esters RSe—CS—Cl with R = C2H5 and nC3H7 have been prepared by reaction of thiophosgene with the corresponding alkane selenol. The compounds have been characterized with electron absorption, nuclear magnetic resonance (1H, 13C, and 77Se), infrared, and mass spectra.
    Notes: Die bisher nicht bekannten Ester RSe—CS—Cl mit R = C2H5 und nC3H7 wurden durch Umsetzung von Thiophosgen mit dem entsprechenden Alkanselenol hergestellt. Die Verbindungen wurden mit Elektronenabsorptions-, 1H-, 13C- und 77Se-NMR-, Infrarot- und Massenspektren charakterisiert.
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    Zeitschrift für anorganische Chemie 509 (1984), S. 95-100 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon and Germanium. XXXIV. A Further Contribution to the Preparation of Potassium SilylThe reaction time for the preparation of potassium silyl from monosilane in glyme is abridged considerably by the use of dispersed Na/K alloy. The preparation is simplyfied by the use of pure dispersed potassium instead of the dispersed alloy. In this case a further abridgement of the reaction time is observed and the filtration of the residue after the end of the reaction is easier because there is no sodium in the residue. Crystalline potassium silyl, free of potassium hydride and glyme, is obtained by recrystallisation followed by slow crystallisation from a glyme/benzene mixture. During a storage of 30 month the crystals turned out to be stable.
    Notes: Die Reaktionszeit für die Darstellung von Kaliumsilyl aus Monosilan in Monoglyme verkürzt sich bei Verwendung von dispergierter Na/K-Legierung erheblich. Die Darstellung vereinfacht sich, wenn statt der dispergierten Na/K-Legierung reines dispergiertes Kalium eingesetzt wird. Hierbei wird eine weitere Verkürzung der Reaktionszeit festgestellt, und die Filtration des Rückstandes nach Ende der Reaktion ist durch das Fehlen des Natriums einfacher. Kaliumsilylkristalle, in denen weder Kaliumhydrid noch Monoglyme nachweisbar sind, werden durch Umkristallisieren und nachfolgende langsame Kristallisation aus einem Monoglyme/Benzol-Gemisch erhalten. Die Kristalle erwiesen sich bei einer 30monatigen Lagerung als stabil.
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  • 82
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    Zeitschrift für anorganische Chemie 509 (1984), S. 127-137 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Oxothorates of the Alkaline Metals: K3NaTh2O6For a first time single crystals of a (in addition: new) oxothorate were prepared starting with the binary oxides [1 200°C, 4d, then 1 300°C, 5d, Ni-bomb; powder: 650°C, 10d, Ag-bomb]. The colourless, transparent single crystals are monoclinic, C2/c, a = 629.64 pm, b = 1 089.93 pm, c = 1 259.75 pm, β = 99.66°, z = 4, Dx = 5.458 g cm-3 and Dpyc = 5.456 gcm-3. It is an ordered variant of the NaCl-type; MoKα, fourcircle diffractometer data (PW 1100), R = 7.67 and Rw = 7.35% for 1 083 of 1 236 I0 (hkl). The Madelung Part of Lattice Energy, MAPLE, is calculated and discussed.
    Notes: Erstmals wurden Einkristalle eines zudem neuen Oxothorates, K3NaTh2O6, aus den binären Komponenten dargestellt [1 200°C, 4d, dann 1 300°C, 5d, Ni-Bömbchen; Pulver analog: 650°C, 10d, Ag-Bömbchen]. Die farblosen, durchsichtigen Einkristalle kristallisieren monoklin, C2/c, a = 629,64 pm, b = 1 089,93 pm, c = 1 259,75 pm, β = 99,66°, Z = 4, drö = 5,458 g cm-3 und dpyk = 5,456 g cm-3. Es liegt eine geordnete NaCl-Variante vor; MoKα, Vierkreisdiffraktometerdaten (PW 1100), R = 7,67 und Rw = 7,35% für 1 083 von 1 236 I0(hkl). Der Madelunganteil der Gitterenergie, MAPLE, wird berechnet und diskutiert.
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  • 83
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    Zeitschrift für anorganische Chemie 509 (1984), S. 153-160 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrate-, Thiosulphate-, Sulphate-, and Sulphide Cancrinite1For the synthesis of the compounds to a solution of sodium aluminate there is added in excess sodium nitrate, or sodium thiosulphate, or sodium sulphite, or sodium sulphide. After heating a solution of sodium silicate is added, and the suspension is hold at 110°C for a long time, the precipatite is filtered, washed, and dried.2The white compounds are characterized in composition and crystal structure by chemical and X-ray analysis and densities.3The unimolecular hexagonal cell of the compounds has the cancrinite structure (lattice constants and densities see „Inhaltsübersicht“).4By heating of thiosulphate cancrinite at 1 000°C in air there is produced a nice deep blue coloured pigment.
    Notes: 1Zur Darstellung der Verbindungen wird zu einer Natriumaluminatlösung Natriumnitrat oder Natriumthiosulfat oder Natriumsulfat oder Natriumsulfid bei Zimmer-temperatur im Überschuß gegeben. Nach Aufheizen wird eine Wasserglaslösung zugetropft, die Suspension längere Zeit bei 110°C gehalten, der Niederschlag abfiltriert, gewaschen und getrocknet.2Die weißen Verbindungen werden in Zusammensetzung und Kristallstruktur durch chemische und röntgenographische Analyse sowie Dichten charakterisiert.3Mit 1 Molekel/Zelle kristallisieren die Verbindungen im hexagonalen Cancrinitgitter mit den Konstanten und Dichten: TextVerbindungGitterkonstanten in ÅDichten in g/ml a0c0RöntgenPyknometerNa8[Al6Si6O24](NO3)2 · 4 H0O12,68 ± 0,025,18 ± 0,012,522,30Na8[Al6Si6O24](S2O3) · 3 H2O12,73 ± 0,025,02 ± 0,032,512,28Na8[Al6Si6O24](SO4) · 3 H2O12,674 ± 0,0045,173 ± 0,0032,422,37Na8[Al6Si6O24](S) · 4 H2O12,669 ± 0,0075,187 ± 0,0032,312,244Durch Glühen des Thiosulfat-Cancrinits bei 1 000°C an Luft erhält man ein schönes tiefblaues Pigment.
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  • 84
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    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 510 (1984) 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 85
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    Zeitschrift für anorganische Chemie 510 (1984), S. 11-15 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Benzyl Nickel(II) Complexes and their ReactionsBy the oxydative addition of p-substituted benzyl chlorides to (Ph3P)2Ni(C2H4) at -20°C the violet nickel(II) complexes (Ph3P)2Ni(p-CH2C6H4R)Cl (R = CN, COOH, CH3, Cl) are, formed. In water containing solutions the carbonic acid (Ph3P)2Ni(p-CH2C6H4COOH)Cl is rearranged to the corresponding p-methylbenzoate.With carbon dioxide the complexes (Ph3P)2Ni(p—CH2C6H4R)Cl react like Grignard compounds. Diphenyl ethine and butadien-1,3 are inserted in the Ni - C bond at room temperature. Substituted nickel-σ-vinyl or π-allyl complexes are obtained. The reactivity of the nickel-σ-benzyl compounds is compared with that of other nickel(II)-alkyl compounds.
    Notes: Die oxydative Addition von p-substituierten Benzylchloriden an (Ph3P)2—Ni(C2H4) bei -20°C ergibt die violetten Nickel(II)-Komplexe (Ph3P)2Ni(p—CH2C6H4R)Cl (R = CN, COOH, CH3, Cl). Die Carbonsäure (Ph3P)2Ni(p—CH2C6H4COOH)Cl lagert sich in Gegenwart von Wasser in das entsprechende p-Methylbenzoat ein.Die Verbindungen des Typs (Ph3P)2Ni(p—CH2C6H4R)Cl reagieren mit Kohlendioxid grignardanalog. Diphenylethin und Butadien-1,3 werden bei normaler Temperatur in die Ni - C-Bindung eingeschoben. Dabei entstehen substituierte Nickel-σ-vinyl- bzw. π-allyl-Komplexe. Das Reaktionsverhalten der Nickel-σ-benzylverbindungen wird mit dem anderer Nickel(II)-alkylverbindungen verglichen.
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  • 86
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    Zeitschrift für anorganische Chemie 510 (1984), S. 46-50 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung und Kristallstrukturbestimmung von La3ReO8La3ReO8 wurde bei 1425°C dargestellt, die Strukturbestimmung ergab abweichende Resultate von einer Darstellung, die bei 900°C erfolgte (BAUD u. Mitarb. 1979). Die Hochtemperaturmodifikation kristallisiert in der monoklinen Raumgruppe P21/m mit a = 7,757(1), b = 7,777(1), c = 5,928(1) Å, γ = 111,1°, Z = 2. Die Struktur wurde durch Patterson und Fouriersynthesen gelöst und bis R(F) = 0,073 verfeinert. Die Struktur besteht aus isolierten, verzerrten ReO6-Oktaedern und Doppelketten von kantenverknüpften La4O-Tetraedern.
    Notes: The crystal structure of La3ReO8, prepared at 1425°C, is reported to be different from a previous result on a preparation at 900°C (BAUD et al., 1979). The high temperature modification crystallizes in the monoclinic space group P21/m with a = 7.757(1), b = 7.777(1), c = 5.928(1) Å, γ = 111.1°, Z = 2. The structure was solved by Patterson and Fourier methods from single crystal diffractometer data and refined to final R(F) = 0,073. The structure consists of isolated, distorted ReO6 octahedra and double chains of edge-shared La4O tetrahedra.
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  • 87
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    Zeitschrift für anorganische Chemie 510 (1984), S. 72-78 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Resonance Raman Spectrum and Structure of Matrixisolated Te3By condensing a mixture of 76% Te atoms and 24% Te2 molecules in a nitrogen matrix at 15 K followed by annealing to nearly 25 K we obtained Te3 molecules by a matrix reaction. The resonance Raman spectrum of Te3 contains 8 overtones of the symmetric stretching vibration. The following values for ω1 and x11 have been calculated for the isotopically pure species 126Te3: ω1 = 206.33 ± 0.15 cm-1; x11 = 0.24 ± 0.03 cm-1 and 130Te3: ω1 = 203.1 ± 0.2 cm-1; x11 = 0.22 ± 0.05 cm-1. Using a 1:1 ratio of 126Te and 130Te in the synthesis of Te3 the band shape of the envelopes of the superimposed spectra of all possible Te3 species could only be explained assuming a bent structure (120° ± 10°). The value of the force constant fr + frr of 210 ± 10 Nm-1 reflects multiple bonding in this molecule. The proposed structure also agrees with thermodynamical considerations.
    Notes: Wird eine Gasmischung aus 76% Te-Atomen und 24% Te2-Molekeln mit einem Überschuß Stickstoff bei 15 K abgeschreckt und anschließend kurz auf 25 K erwärmt, so entstehen durch eine Matrixreaktion Te3-Molekeln. Im Resonanzramanspektrum dieser Spezies werden 8 Obertöne der symmetrischen Streckschwingung beobachtet. Für zwei verschiedene Te-Isotope erhält man folgende Werte für ω1 und x11: 126Te3: 206,33 ± 0,15 cm-1, 0,24 ± 0,03 cm-1; 130Te3: 203,1 ± 0,20 cm-1, 0,22 ± 0,05 cm-1. Die Verwendung von Proben, die je 50% der beiden Isotopen enthalten führt zu einem Bandenmuster, bei dem die Intensität der einzelnen Banden und ihre Frequenzverschiebung für eine gewinkeltes Te3-Molekel sprechen (120° ± 10°). Der Wert der Kraftkonstante fr + frr von 210 ± 10 Nm-1 zeigt Mehrfachbindungsanteile an. Eine thermodynamische Betrachtung liefert zusätzliche Anhaltspunkte für eine offene (nicht ringförmige) Struktur vom Te3.
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  • 88
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    Zeitschrift für anorganische Chemie 510 (1984), S. 104-108 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Trialkylbismutines as Ligands in Carbonyl Complexes of Iron and Group VIa ElementsThe complexes (CO)4FeBiR3 (R = Et, Pr, Bu) are synthesized by reaction of Fe2(CO)9 and the corresponding bismutines. Complexes of the type Bu3BiM(CO)5 (M = Cr, Mo, W) are formed by irradiation of the hexacarbonyls of group VIa elements in tetrahydrofuran and subsequent addition of Bu3Bi. The novel compounds are obtained in 40 - 90% yield. They are stable in an inert atmosphere above 25°C. Their 1H-n. m. r., i. r., and m. s. data are discussed.
    Notes: Die Komplexe (CO)4FeBiR3 (R = Et, Pr, Bu) werden durch Umsetzung von Fe2(CO)9 mit den entsprechenden Bismutinen synthetisiert. Komplexe des Typs Bu3BiM(CO)5 (M = Cr, Mo, W) entstehen durch Bestrahlung der Hexacarbonyle der VIa-Elemente in Tetrahydrofuran und nachfolgende Umsetzung mit Bu3Bi. Die neuen Verbindungen werden in 40 - 90% Ausbeute erhalten. Sie sind bei Luftausschluß auch oberhalb von 25°C stabil. Ihre 1H-NMR-, IR- und EI-MS-Daten werden diskutiert.
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  • 89
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    Zeitschrift für anorganische Chemie 510 (1984), S. 143-151 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structure of Ag2Ge2O5: A New Ge2O52- Network StructureAg2Ge2O5 was prepared from the binary oxides at high O2 pressures. Single crystal X-ray diffraction work indicated monoclinic symmetry (P21/c; a = 1101.3(2); b = 1006.3(1); c = 1221.9(3) pm; ß = 94.6(1)°). The structure was determined by direct methods (3372 independent structure factors) and refined to a conventional R value of 0.084. A new Ge2O52- network structure was found with germanium coordinated octahedrally (­d(Ge - O) = 188,7 pm) and tetrahedrally (­d(Ge - O) = 175,9 pm), in equal proportions, by oxygen. The polyhedra share vertices and edges, thus forming a three dimensional channel system, which is occupied by Ag+ ions. The shortest Ag - Ag distance of 284 pm, like the pale yellow colour of the compound, indicates Ag+ - Ag+ interaction.
    Notes: Durch Sauerstoffhochdrucksynthese wurde Ag2Ge2O5 aus den binären Komponenten dargestellt. Nach Einkristalluntersuchungen liegt monokline Symmetrie vor (P21/c; a = 1101,3(2); b = 1006,3(1); c = 1221,9(3) pm; ß = 94,6°(1); Z = 12). Die Struktur wurde mittels direkter Methoden (Ag-Positionen) und Fourier-Synthesen gelöst (3372 unabhängige Strukturfaktoren); der R-Wert konvergierte bei 8,4%. Das Anion Ge2O52- bildet eine neuartige Raumnetzstruktur, wobei die Germaniumatome jeweils zur Hälfte oktaedrisch [­d(Ge - O) = 188,7 pm] und tetraedrisch [­d(Ge - O) = 175,9 pm] von Sauerstoff koordiniert sind. Die Polyeder sind in der Weise über gemeinsame Ecken und Kanten verknüpft, daß dreidimensional vernetzte, kanalartige Hohlräume entstehen, die von den Gegenkationen (Ag+) ausgefüllt werden. Der kürzeste Ag - Ag-Abstand beträgt 284 pm und gibt, wie die blaßgelbe Eigenfarbe der Substanz, einen Hinweis auf bindende Ag+ - Ag+-Wechselwirkungen.
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  • 90
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    Zeitschrift für anorganische Chemie 510 (1984), S. 175-179 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Bis- and Tris(trimethylsilyl)-methyl-aminofluorosilanesLithium-tris(trimethylsilyl)methane reacts with fluoro-silanes to give (Me3Si)3C - SiF2R (1 - 3, R = F, C6H5, CMe3). 1 and 2 react with lithiated amines to aminofluorosilanes 4 a, 5 a, 6 a, and with a 1, 3-migration of a silyl group to the structure isomeric trimethylsilylaminofluorsilanes 4 b, 5 b, 6 b, 7, 8. The disubstituted NH-compound 9 is obtained in the reaction of 1 with LiNH2.
    Notes: Lithium-tris(trimethylsilyl)-methan reagiert mit Fluorsilanen unter Substitution zu (Me3Si)3CSiF2R (1 - 3, R = F, C6H5, CMe3). Mit lithiierten Aminen reagieren 1 und 2 zu den Aminofluorsilanen 4a, 5a, 6a, und unter 1, 3-Silylgruppenwanderung zu den strukturisomeren Trimethylsilylaminofluorsilanen 4 b, 5 b, 6 b, 7, 8. In der Reaktion von 1 mit LiNH2 wird die disubstituierte NH-Verbindung 9 erhalten.
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  • 91
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    Zeitschrift für anorganische Chemie 514 (1984), S. 69-71 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tris-trimethylsilyl-tert.butyl-cyclotetraphosphaneP4(SiMe3)3CMe3 1, which was previously unknown in the series of the cyclotetraphosphanes P4(SiMe3)nCMe34-n, n = 0-4, could be obtained by the reaction of P3(SiMe3)5 with Me3CPCl2. 1 froms intensely coloured yellow crystals, melting point 143 ± 2°C. The 31P- and 1H-NMR data of 1 are given.
    Notes: Das in der Reihe der Cyclotetraphosphane P4(SiMe3)n(CMe3)4-n, n = 0-4, bisher noch unbekannte P4(SiMe3)CMe3 1 konnte durch Umsetzung von P3(SiMe3)5 mit Me3CPCl2 dargestellt werden. 1 bildet intensiv gelbe Kristalle, Schmp. 143 ± 2°C. Die 31P- und 1H-NMR-Daten von 1 werden angegeben.
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  • 92
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    Zeitschrift für anorganische Chemie 514 (1984), S. 72-78 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [PPh3Cl]⊕[ReCl4(N2S2)]⊖; Synthese, IR-Spektrum und Kristall StruktureThe title compound is prepared by the reaction of [ReCl3(NSCl)2(POCl3)] with triphenylphosphane; it formes black crystals. The crystal structure determination was solved with X-ray methods (2861 observed independent reflexions, R = 0.038). The compound crystallizes monoclinic in the space group P21/n with four formula units per unit cell. The structure consists of [PPh3Cl]⊕ cations and [ReCl4(N2S2)]⊖ anions, in which the rhenium atom is surrounded octahedrally by four chlorine ligands and the N atoms of a ReN2S2-five-membered ring in cis-position (symmetry C2v). The Re—N bond lengths (181 pm) and the NS bond lengths (152 pm) are in the range of double bonds; the S—S distance is very long (253 pm). The i.r. spectrum is reported.
    Notes: Die Titelverbindung entsteht in Form schwarzer Kristalle bei der Reaktion von [ReCl3(NSCl)2(POCl3)] mit Triphenylphosphan. Die Kristallstruktur wurde mit Hilfe von Röntgenbeugungsdaten ermittelt ermittelt (2861 beobachtete unabhängige Reflexe, R = 0,038). Die Verbindung kristallisiert monoklin in der Raumgruppe P21/n mit vier Formeleinheiten pro Elementarzelle. Die Struktur besteht aus [PPh3Cl]⊕-Kationen und Anionen [ReCl4(N2S2)]⊖, in denen das Rhenium oktaedrisch von vier Chlorliganden und den beiden cis-ständigen Stickstoffatomen eines ReN2S2-Fünfringes umgeben ist (Symmetrie C2v). Die ReN-Abstände (181 pm) und die NS-Abstände (152 pm) entsprechen etwa Doppelbindungen; die S—S-Bindungslänge ist mit 253 pm sehr lang. Das IR-Spektrum wird mitgeteilt.
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  • 93
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    Zeitschrift für anorganische Chemie 514 (1984), S. 92-98 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Fluorides of Divalent Lanthanoids. II. Synthesis of MLnF3 from MLnF4CsEuF3, CsYbF3, and RbYbF3, which had already been prepared via reduction of the corresponding trifluorides with alkali metal, were also obtained by reducing MLnF4 with M (M = Cs, Rb, K; Ln = Eu, Yb). No additional alkali fluoroperovskites of lanthanoids were detected either by reduction of LnF3 or MLnF4 with metallic Cs, Rb, or K or by other reactions, e.g. 3CsF + 2SmF3 + Sm. It was shown that the reaction of CsF with EuF2 (350-850°C) produced only very little CsEuF3.
    Notes: CsEuF3, CsYbF3 und RbYbF3, zuvor nur durch Reduktion von EuF3 bzw. YbF3 mit met. Cs bzw. Rb erhalten, entstehen auch bei der Reduktion von MLnF4 mit M (M = Cs, Rb, K; Ln = Eu, Yb). Weitere unbekannte Perowskite wie CsSmF3 erhält man auf diesem Wege nicht. Tempern von innigen Gemengen der binären Fluoride (z.B. CsF + EuF2) führt nur zu sehr unvollständiger Umsetzung. Auch Synthesen durch Komproportionierung (z. B. 3CsF + 2SmF3 + Sm) sind ohne Erfolg. Durchgeführt wurden alle Reduktionen von LnF3 (Ln = Sm, Eu, Tm, Yb) mit M (M = Cs, Rb, K).
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    Zeitschrift für anorganische Chemie 514 (1984), S. 120-128 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Chalcogenolates. 139. Studies on Dialkyl Esters of Chalcogenocarbonic Acids. 2. O,Se- and S, Se-Dialkyl MonothiomonoselenocarbonatesThe hitherto unknown esters RSe—CS—OR′, where R = C2H5, nC3H7 and R′ = C2H5, nC3H7, are formed by reaction of NaSeR with Cl—CS—OR′ and of RSe—CS—Cl with HOR′. At the first time, the esters RSe—CO—SR′ with R = R′ = C2H5, nC3H7 have been prepared by reaction between NaSeR and Cl—CO—SR′. The compounds have been characterized by means of diverse spectroscopic methods.
    Notes: Die bisher nicht bekannten Ester RSe—CS—OR′ mit R = C2H5, nC3H7 und R′ = C2H5, nC3H7 entstehen bei der Reaktion von NaSeR mit Cl—CS—OR′ und bei der von RSe—CS—Cl mit HOR′. Erstmals wurden die Ester RSe—CO—SR′ mit R = R′ = C2H5, nC3H7 durch Umsetzung von NaSeR mit Cl—CO—SR′ hergestellt. Die genannten Verbindungen wurden mit Hilfe verschiedener spektroskopischer Methoden charakterisiert.
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  • 95
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    Zeitschrift für anorganische Chemie 514 (1984), S. 107-114 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Sulfur Nitrogen Compounds. 16. Products of the Reaction of Lead- and Tin Salts with S4N4. Structures of PbN2S2 · NH3, PbN2S2, and SnCl4 · 2S4N4PbN2S2 · NH3 is monoclinic, P21/a, a = 5.671, b = 16.123, c = 6.102 Å, β = 95.12°, Z = 4, PbN2S2, however, orthorhombic, P212121, a = 4.375, b = 7.654, c = 12.274 Å, Z = 4. The planar five-membered PbN2S2 rings in both compounds show no remarkable differences. In PbN2S2 · NH3, the NH3 molecule is bound to Pb perpendicularly to the plane of the ring.The structure of the long known addition compound SnCl4 · 2S4N4 was determined. It is orthorhombic, Pc21b, a = 11.467, b = 11.995, c = 12.374 Å, Z = 4. Sn shows sixfold coordination, the two S4N4 rings are attached to Sn trans to each other via a N atom.
    Notes: PbN2S2 · NH3 kristallisiert monoklin, Raumgruppe P21/a mit a = 5,671 Å, b = 16,123 Å; c = 6,102 Å, β = 95,12°, Z = 4, PbN2S2 dagegen orthorhombisch, Raumgruppe P212121 mit a = 4,375 Å, b = 7,654 Å, c = 12,274 Å, Z = 4. Die ebenen fünfgliedrigen PbN2S2-Ringe beider Verbindungen unterscheiden sich nur unwesentlich. Bei PbN2S2 · NH3 ist an Pb zusätzlich noch ein NH3-Molekül senkrecht zur Ringebene gebunden.Von der schon lange bekannten Additionsverbindung SnCl4 · 2S4N4 konnte ebenfalls die Struktur bestimmt werden: orthorhombisch, Raumgruppe Pc21b mit a = 11,467 Å, b = 11,995 Å, c = 12,374 Å, Z = 4. Sn ist 6fach koordiniert, die beiden S4N4-Ringe sind über je ein N-Atom in Transstellung an Sn gebunden.
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  • 96
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Structure of Ill-crystallized Calcium Hydrogen Silicates. VI. Chemical, ESR, and Mössbauer-Spectroscopic Investigations on the Incorporation of Fe3+ into C—S—H(Di, Poly)C—S—H(Di, Poly), prepared by precipitation reactions from sodium silicate solutions in presence of Fe3+ ions, incorporates at least up to 0.09 Fe2O3/SiO2. Thereby the anion composition of the C—S—H(Di, Poly) ist not affected.The results of ESR and Mössbauer spectroscopic measurements show, that Fe is incorporated as Fe3+ at octahedral sites. Only less than 1% of the total amount of Fe3+ is situated at tetrahedral sites. In good accordance with that is the change of thermal stability of the silicate anions concerning condensation and degradation reactions.
    Notes: In C—S—H(Di, Poly), das bei 80°C (353 K) über Fällungsreaktionen aus Natriumsilicatlösungen in Gegenwart von Fe3+-Ionen synthetisiert wurde, lassen sich bis mindestens 0,09 Fe2O3/SiO2 einbauen. Der Anionenaufbau des C—S—H(Di, Poly) wird dadurch nicht verändert. Aus ESR- bzw. Mößbauer-spektroskopischen Befunden geht hervor, daß das Eisen als Fe3+ hauptsächlich auf Oktaederplätzen vorliegt, während Tetraederplätze nur von weniger als 1% der Gesamteisenmenge besetzt werden. Die Änderung der thermischen Stabilität der Silicatanionen gegenüber Kondensations- und Abbaureaktionen steht mit dem Einbau von Fe3+ auf Oktaederplätzen in guter Übereinstimmung.
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  • 97
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Lower Chalcogen Fluorides. IX. Preparation and Characterization of SF3SSFDuring cocondensation of SF2 and SSF2 the new compound 1,3-Difluorotrisulphane-1,1-difluoride is formed in low yield and can be isolated by means of low temperature fractionation. The compound was unequivocally characterized by 19F-n.m.r,i.r.,Raman, and mass spectra. The unstable compound ist a colourless, viscous liquid with an extrapolated boiling point of 94°C and a melting point of -62°C. It decomposes to SF4 and SSF2 in the gas phase.
    Notes: Bei der Cokondensation von SF2 und SSF2 entsteht in geringen Ausbeuten die neue Verbindung 1,3-Difluor-trisulfan-1,1-difluorid, SF3SSF, die mittels Tieftemperaturfraktionierung isoliert werden konnte. Durch 19F-NMR-, IR-, Raman- und Massenspektren wurde die Verbindung eindeutig charakterisiert. Das sehr zersetzliche SF3SSF ist eine farblose, viskose Flüssigkeit mit einem extrapolierten Siedepunkt von 94°C und einem Schmelzpunkt von -62°C. Es zerfällt in der Gasphase in SF4 und SSF2.
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  • 98
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 514 (1984), S. 205-212 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bildung und Zersetzung von LanthanoxidcarbonatAmorphes Lanthancarbonat wird durch Hydrolyse von Lanthanisopropoxid mit wäßriger Ammoniaklösung an Luft dargestellt. Lanthanoxidcarbonat, La2O(CO3)2 · H2O, kristallisiert, wenn die amorphe Substanz mit heißem Wasser gewaschen wird. Die Kristallisation und das thermische Verhalten des kristallinen Materials werden röntgenographisch, thermoanalytisch und IR-spektroskopisch untersucht. Die Zersetzung des La2O(CO3)2 · H2O in das IA-(LaO)2CO3 wird bei 440 bis 540°C beobachtet. Die Zersetzungsisothermen können durch eine gebrochene rationale Funktion beschrieben werden; die Aktivierungsenergie beträgt 42,6 kcal · mol-1. IA-(LaO)2CO3 zersetzt sich dann zum A-La2O3 bei 750 bis 870°C. Die Kinetik wird ebenfalls durch eine gebrochene rationale Funktion interpretiert; die Aktivierungsenergie beträgt 58,3 kcal · mol-1.
    Notes: Amorphous lanthanum carbonate was prepared by hydrolysis of lanthanum isopropoxide using ammonia water in the atmosphere. Lanthanum monoxocarbonate, La2O(CO3)2 · H2O, crystallizes when this amorphous material was washed with hot water. The crystallization and thermal behavior of the crystalline material are studied by X-ray diffraction, thermal analysis, and infrared spectroscopy. The decomposition of La2O(CO3)2 · H2O into type-IA (LaO)2CO3 is observed at 440 to 540°C. Decomposition isotherms are described by the contracting cube equation, the activation energy being 42.6 kcal mol-1. Type-IA (LaO)2CO3 subsequently decomposes to A-type La2O3 at 750 to 870°C. The kinetics is also interpreted in terms of the contracting cube equation, the activation energy being 58.3 kcal mol-1.
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  • 99
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 514 (1984), S. 240-240 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 100
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structural Chemistry of Phosphorus Containing Chains and Rings. 11. Crystal and Molecular Structures of the Two Stereoisomers of Tetraphospha-silaspiro[2.2]pentane (PBut)2Si(PBut)2The spirocyclic compound 1,2,4,5-tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentane exists in tow diastereomers of point symmetry 4 and 2. The isomer with symmetry 4 even in the solid crystallizes tetragonally in I41/a with a = 1247.0, c = 1505.5 pm and Z = 4. The isomer of fairly exact symmetry 2 crystallizes triclinically in P1 with a = 612.8, b = 996.3, c = 1017.2 pm, α = 75.63, β = 72.38, γ = 88.71° and Z = 1. In this disordered structure the surroundings of Si is slightly distorted due to the influence of the substituents. The (average) bond lengths are (4, 2): d(Si—P) = 220.09(9), 221.5(5); d(P—P) = 225.5(2), 224.2(5); d(P—C) = 189.4(3), 190(2); d(C—C) = 151.4(4), 152(3) pm. The geometry of the substituents in both isomers is quite normal.
    Notes: Die Spiroverbindung 1,2,4,5-Tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentan liegt in zwei Diastereomeren der Punktsymmetrie 4 und 2 vor. Das Isomer der auch im Festkörper exakten Symmetrie 4 kristallisiert tetragonal in der Raumgruppe I41/a mit a = 1247,0, c = 1505,5 pm und Z = 4. Das sterisch weniger günstige Isomer der im Festkörper nicht streng erfüllten Symmetrie 2 kristallisiert triklin in der Raumgruppe P1 mit a = 612,8, b = 996,3, c = 1017,2 pm, α = 75.63, β = 72,38, γ = 88,71° und Z = 1. In dieser nur fehlgeordnet beschreibbaren Struktur wird die Umgebung des Si durch Substituenteneinflüsse etwas verzerrt. Die (mittleren) Bindungslängen betragen (4, 2): d(Si—P) = 220,09(9), 221,5(5); d(P—P) = 225,5(2), 224,2(5); d(P—C) = 189,4(3), 190(2); d(C—C) = 151,4(4), 152(3) pm. Die Geometrie der Substituenten ist in beiden Isomeren normal.
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