ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Wiley-Blackwell  (13)
  • Blackwell Publishing Ltd  (2)
  • American Geophysical Union (AGU)
  • American Meteorological Society (AMS)
  • 1985-1989  (7)
  • 1980-1984  (8)
Collection
Years
Year
  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 483 (1981), S. 193-204 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung, Eigenschaften und ESCA-Charakterisierung von Vanadium-Oberflächenverbindungen an Silicagel. IIBindungsenergiewerte (BE) und Intensitätsverhältnisse in Vn/SiO2 (n = 3, 4 und 5) in Abhängigkeit von der Vanadium-Konzentration und Liganden L wurden untersucht. Die Ermittlung optimierter Produkte und ESCA-Proben wird beschrieben. Anhand dieser Ergebnisse werden die Bedingungen demonstriert, unter denen ESCA zuverlässige Informationen über feinverteilte Oberflächen-Verbindungen liefern kann.Der geeignete Konzentrationsbereich für wäßrige Dotierungen liegt zwischen 0,4 bis 1,2% VIII und 1,0 bis 1,2% für VV; in nichtwäßrigen (metallorganischen) Präparaten ergeben sogar 0,15 bis 0,4% VIII und 0,4% VV brauchbare Spektren. Die ESCA-Daten des Peroxo-Komplexes (≡Si—O)3V—(O2) (I) Bestätigen diese Trends.Außerordentlich feinverteilte Oberflächen-Verbindungen erhält man aus Dotierungen mit V[N(SiMe3)2]3. Hier ist eine Konzentration von 0,4 bis 0,5% VIII (oder VV) optimal und die obere Grenze.Beweise für die Formulierung von VnSiO2 als dreibeinige Oberflächen-Verbindungen sind zusammengefaßt; die Bedeutung des Additivitätsprinzips für die Erklärung und Voraussage elektronischer Verhältnisse bei Oberflächen-Verbindungen wird erläutert.Innerhalb der Serie (≡SiO)3V—L (mit L = ohne Liganden, =0, und —Oz) wurden die chemischen Verschiebungen für ≡Si—O—V (0,7 eV); V=O (0,6 eV) und V—(O2) (0,4 eV) ermittelt. Die BE-Beiträge einiger Donorliganden (und —Cl) werden abgeschätzt. In (I)deuten die ESCA-Daten eine formale Oxydationszahl nahe +4 an.Grenzen der ESCA-Methode werden erwähnt und Erweiterungen des Additivitätsprinzips diskutiert.
    Notes: Binding energy (BE) behavior and signal intensity as function of V conc. and ligands L were critically examined in Vn/SiO2 species (where n = +5, +4, and +3) and securing of optimized products and ESCA samples is described. The results moreover demonstrate conditions and approaches whereby ESCA can provide reliable information on highly diluted surface compound systems.From aquous media 1.0-1.2 wt. % VV and 0.4-1.2 wt. % VIII proved to be preferred ranges whereas in non aqueous (metalorganic) preparates the surprisingly low concentration of 0.4-0.15 wt. % VIII gave usable spectra and even 0.4 wt. % VV could be measured. ESCA data with the peroxo complex (≡Si—O)3V—(O2) (I) confirmed these trends.Superiorly subdivided surface compounds (reflected in the quality of spectra) are obtainable from V[N(SiMe3)2]3 impregnations where 0.4-0.5 wt. % VIII (or VV) are maximum/optimum conc. limits.Evidence for formulating Vn/SiO2 as three legged surface compounds is summarized and diagnostic/predictive uses of the additivity principle for surface electron states illustrated.In the (≡Si—O)3V—L series, where L = none, =O, and —(O2) positive ΔBE shifts for ≡Si—O—V (0.7 eV); V=O (0.6 eV); and V—(O2) (0.4 eV) were estimated. Tentative BE contributions of some donor ligands (and —Cl) are also suggested. In (I) ESCA indicated a formal oxidation state of approx. +4.Certain limits (precautions) with ESCA are noted and extensions of the additivity relationship discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 462 (1980), S. 177-184 
    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. XXX. Synthesis and Characterization of Nitrobenzyl Nickel Compounds(C2H5)2Ni · dipy reacts with benzyl chlorides forming complexes of the type RNiCl · dipy. In this way nitro groups containing thermally stable organonickel compounds can be obtained, which cannot be achieved by means of organolithiiim or Grignard reagents. - In a similar way (C2H5)Ni · dipy reacts with to form · dipy.The composition of the compounds achieved was proved by analysis, by characteristic reactions, magnetic moments, and in part by their IR and M spectra.
    Notes: (C2H5)2Ni · dipy reagiert mit Benzylchloriden zu Benzylnickelchlorid-Komplexen des Typs RNiCl · dipy. Auf diesem Wege sind auch Nitrogruppen enthaltende thermisch stabile Organonickelverbindungen zugängig, die mittels Organolithium-oder Grignardverbindungen nicht erhalten werden können. - Auf analoge Weise reagiert (C2H5)2Ni · dipy mit zu · dipy.Die Zusammensetzung der erhaltenen Verbindungen wurde analytisch, durch die magnetischen Momente sowie IR-Daten und M-Spektren und durch charakteristische Reaktionen gesichert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 483 (1981), S. 205-218 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung, Eigenschaften und ESCA-Charakterisierung von Vanadium-Oberflächenverbindungen an Silicagel. III.Die leicht darstellbaren Hexamethyldisilazen-Derivate der Übergangsmetalle (z. B. M—HMDS) werden als neuartiges Reagenz zur Darstellung von Oberflächen-Verbindungen des Typs ≡Si—O—M beschrieben. Folgeprodukte dieser Umsetzungen, ≡Si—O—SiMe3 und ≡Si—N(SiMe3)2, schaffen dabei eine hydrophobe Umgebung, die durch Temperaturerhöhung (300-400°C) beseitigt werden kann. Die Reaktionsfähigkeit der M—N-Bindungen mit Oberflächen-Silanolgruppen und gespannten Siloxaneinheiten kann durch eine Koordination von Liganden L (auch Lösungsmittelmoleküle) beeinflußt werden.Dreibeinige Vanadium(III)-Oberflächen-Verbindungen lassen sich direkt durch thermisches Aktivieren von V[N(SiMe3)2]3 auf SiO2 in neutraler oder reduzierender Atmosphäre erhalten. Der Reaktionsablauf wurde anhand von ESCA- und Reflexionsspektren verfolgt. Dotierungen aus benzolischer Lösung (0,40-0,45 % V) bei anschließendem Erhitzen auf 400-800°C ergaben optimierte Produkte.Auf diese Weise optimiertes (≡Si—O)3V ergab identische Spektren und die gleichen chemischen und katalytischen Eigenschaften wie die Oxydations-/Reduktions-Produkte aus wäßrigen Dotierungen von NH4VO3. Dies ist das erste Beispiel für solch eine bemerkenswerte Übereinstimmung von Oberflächen-Verbindungen, die auf unterschiedlichen Reaktionswegen erhalten wurden. Der Nutzen zur Strukturaufklärung wird unterstrichen.Die Bedeutung der Chemilumineszenz als empfindlichster Indikator für identische Oberflächenzustände wird diskutiert, ebenso wie Versuche, „nacktes“ zweibeiniges VII/Si02 und VIII/SiO, darzustellen.
    Notes: Conveniently available transition metal hexamethyldisilazanes (M-HMDS) are described as novel surface reacting agents in ≡Si—O—M type surface compound formation on silicagel. Secondary reaction products ≡Si—O—SiMe3 and ≡Si—N(SiMe3)2 confer “silanized” (hydrophobic) environments which can be removed at 300-400°C. Reactivity of M—N linkages with surface silanols and strained siloxanes can be manipulated by coordinating ligands L (also as solvents) in the molecule.Three legged vanadium(III) surface compounds were obtained directly by thermal activation of V[N(SiMe3)2]3 on SiO2 in neutral or reducing atmospheres. Detailed course of the reaction were monitored by ESCA and Reflectance Spectroscopy. Impregnation from benzene (0.40-0.45 wt. % V) and subsequent heating to 400-800°C (for 1 hr) gave optimized products.The optimized (≡Si—O)3V from V(HMDS)3 was found to have identical spectral, chemical, and catalytical properties as the oxidation/reduction products from NH4VO3 etc. from aq. impregnations including chemiluminescence with O2 at 20°C. This is the first reported example of such remarkable surface product correspondence by different mechanistic pathways and its utility in structural elucidation is emphasized.Importance of chemiluminescence as most sensitive indicator of identical surface states is discussed as well as attempts to produce “naked” two legged VII/SiO2 and VIII/SiO2.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 14
    ISSN: 0192-253X
    Keywords: Transposable element ; Transcription factor ; Suppression ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We have used the yellow gene of Drosophila melanogaster as a model system in which to study the molecular mechanisms by which the gypsy retrotransposon causes mutant phenotypes that can be reversed by nonalleiic mutations at the suppressor of Hairy-wing locus. This gene encodes a 109,000 dalton protein that contains an acidic domain and 12 copies of the Zn finger motif, which are characteristic of some transcription factors and DNA binding proteins. The suppressible y2 allele is caused by the insertion of the gypsy element at -700 bp from the start of transcription of the Yellow gene, resulting in a phenotype characterized by mouth parts and denticle belts in the larvae, and by bristles in the adults, that show wildtype coloration, but mutant wings and body cuticle in the adult flies. This phenotype is the result of the interaction of gypsy sequences homologous to mammalian enhancers with tissue-specific yellow transcriptional regulatory elements located upstream from the gypsy insertion site and responsible for the expression of the yellow gene in the mutated tissues. This interaction is dependent on the binding of the su(Hw) protein to the specific gypsy sequences involved in the induction of the mutant phenotype.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 15
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman (3500-20 cm-1) and infrared (3500-50 cm-1) spectra of gaseous and solid methylcyclobutane and methyl-d3-cyclobutane have been recorded. Additionally, the Raman spectra of the pure liquids have been recorded and qualitative depolarization values have been obtained. The spectra have been interpreted on the basis that both the axial and equatorial conformers are present in the fluid phases and that the equatorial form is thermodynamically preferred and the only form present in the annealed solid. All 39 of the normal vibrational modes have been assigned for both the d0 and d3 compounds. An abundance of spectral evidence is presented which indicates extensive coupling between the vibrations associated with the ring and those of the methyl group. The CH3 internal torsional mode has been observed in the Raman spectrum of the solid at 232 cm-1 and utilizing this frequency the periodic threefold barrier to internal rotation has been calculated to be 1190 cm-1 (3.40 kcal mol-1). The fundamental ring puckering mode has been assigned from the Raman spectra of the gases to weak features observed at 161 and 154 cm-1 for the d0 and d3 compounds, respectively. All of these results are compared with the corresponding quantities for some similar molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...