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  • Inorganic Chemistry  (315)
  • 1990-1994  (195)
  • 1970-1974  (120)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 416-420 
    ISSN: 0044-2313
    Keywords: Nonaselenide ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of the Nonaselenide [Sr(15-crown-5)2]Se9The title compound was prepared by the reaction of excess selenium with strontium diselenide in DMF in the presence of 15-crown-5. [Sr(15-crown-5)2]Se9 forms black crystals, which are soluble in DMF. They were characterized by FIR spectroscopy and by an X-ray structure determination.Space group P21/n, Z = 4, 2 381 observed unique reflections, R = 0.073. Lattice dimensions at 19°C: a = 1 228.7, b = 1 893.4, c = 1 575.7 pm, β = 99.15°. The compound consists of [Sr(15-crown-5)2]2+ ions in which the strontium ion is coordinated by the oxygen atoms of the crown ether molecules in a sandwich-like fashion, and of Se92- ions with a chain structure, which has a topolocical resemblance with the bicyclic ion Se102-.
    Notes: Die Titelverbindung entsteht durch Einwirkung von überschüssigem Selen auf Strontiumdiselenid in Dimethylformamid (DMF) in Gegenwart von 15-Krone-5. [Sr(15-Krone-5)2]Se9 bildet schwarze, in DMF leicht lösliche Kristalle, die durch das FIR-Spektrum und eine röntgenographische Strukturanalyse charakterisiert werden.Raumgruppe P21/n, Z = 4, 2 381 beobachtete unabhängige Reflexe, R = 0,073. Gitterabmessungen bei 19°C: a = 1 228,7; b = 1 893,4; c = 1 575,7 pm, β = 99,15°. Die Verbindung besteht aus [Sr(15-Krone-5)2]2+-Ionen, in denen das Strontiumion sandwichartig von den O-Atomen der beiden Kronenethermoleküle umgeben ist, und kettenförmigen Se92--Ionen, die topologische Verwandtschaft zu dem bicyclischen Se102--Ion aufweisen.
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Complexes Between Metals and Aromatic Compounds, CXII. Cyclopentadienylcycloheptatrienyl π-Complexes of Molybdenum(0) and Tungsten(0), their Monovalent Cations and a Cyclopentadienylbenzenetungsten(II) HydrideThe synthesis of the diamagnetic, sublimable five-ring seven-ring aromatic metal π-complexes of molybdenum C5H5Mo0C7H7 and tungsten C5H5W0C7H7 via the systems MoCl5/i-C3H7MgBr/C5H5MgBr/ether or WCl6/C2H5Li/C5H5Li/C7H8/ether is described. Both compounds react in benzene with a deficite of iodine to give the paramagnetic monoiodides [C5H5MIC7H7]+I-(M = Mo, W). A new procedure is given for the preparation of C5H5MoIC6H6. Finally experiments to prepare diamagnetic C5H5WIIHC6H6 via the system WCl6/i—C3H7MgBr/C5H5MgBr/1.3—C6H8/ether are reported.
    Notes: Die Synthese der diamagnetischen, sublimierbaren Fünfring-Siebenring-Aromaten-Metall-π-Komplexe des Molybdäns C5H5Mo0C7H7 und Wolframs C5H5W0C7H7 mittels der Systeme MoCl5/iso-C3H7MgBr/C5H5MgBr/C7H8/Äther bzw. WCl6/C2H5Li/C5H5Li/C7H8/Äther wird beschrieben. Beide Verbindungen reagieren in Benzol mit J2 im Unterschuß zu paramagnetischen Monojodiden [C5H5MIC7H7]+J-(M = Mo, W). Ein neues Verfahren zur Darstellung von C5H5MoIC6H6 wird angegeben. Abschließend wird über Versuche zur Darstellung von diamagnetischem C5H5WIIHC6H6 im System WCl6/iso-C3H7MgBr/C5H5MgBr/C6H8-(1.3)/ Äther berichtet.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1892-1904 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Chalkogen Compounds. Preparation, Electronic and Vibrational Spectra of Diphenyldithiophosphinate ComplexesThe preparation and properties of the chelate complexes of the diphenyldithiophosphinate ion Sn(dptpi)2, In(dtpi)3, As(dptpi)3, Sb(dptpi)3, Bi(dptpi)3, Co(dptpi)3, Rh(dptpi)3, Ir(dptpi)3, Pd(dptpi)2, Pt(dptpi)2 and Au(dptpi)3 are reported. From the electronic spectra of various compounds the diphenyldithiophosphinate ion can be placed in the spectrochemical series between the diethyldithiophosphate ion (dtp) and the chloride ion.  -  The nephelauxetic effect is greater than in dtp. Metal-sulfur stretching vibrations for all compounds are found between 270 and 329/cm.
    Notes: Darstellung und Eigenschaften der Chelatkomplexe des Diphenyldithiophosphinat-Ions Sn(dptpi)2, In(dptpi)3, As(dptpi)3, Sb(dptpi)3, Bi(dptpi)3, Co(dptpi)3, Rh(dptpi)3, Ir(dptpi)3, Pd(dptpi)2, Pt(dptpi)2 und Au(dptpi)3 werden beschrieben. Die ligandenfeld-theoretische Ausdeutung der Elektronenspektren verschiedener Komplexe ergibt, daß das Diphenyl-dithiophosphinat-Ion für die meisten Zentralatome (Ausnahme IrIII) in der spektrochemischen Reihe zwischen dem Diäthyldithiophosphat-Ion (dtp) und dem Chlorid-Ion steht.  -  Der nephelauxetische Effekt ist größer als im dtp. Die Metall-Schwefel-Valenzschwingung liegt in allen Verbindungen zwischen 270 und 329/cm.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1905-1914 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Chalkogen Compounds. Preparation, Electronic and Vibrational Spectra of Diphenyldiselenophosphinato ComplexesThe anion of the diphenyldiselenophosphinic acid (dpspi) as a bidentate ligand forms complexes of the type [(C6H5)2PSe2]nM (M=metal). This ligand and its complexes with CoII, NiII, CuI, CdII, and ZnII are reported for the first time. The ligand field splitting parameters are calculated from the electronic spectra of Ni(dpspi)2 and Co(dpspi)2. The position of dpspi in the spectrochemical series is discussed. Its nephelauxetic effect is extremely high. The PSe stretching vibrations of the diphenyldiselenophosphinato complexes are assigned.
    Notes: Das Anion der Diphenyldiselenophosphinsäure („dpspi“) bildet als zweizähniger Ligand Komplexe des Typs [(C6H5)2PSe2]nM (M=Metall). Über diesen Liganden sowie die entsprechenden Komplexe mit CoII, NiII, CuI, CdII und ZnII wird in dieser Arbeit erstmalig berichtet. Aus den Elektronenspektren von Ni(dpspi)2 und Co(dpspi)2 werden die Ligandenfeldparameter berechnet. Die Einordnung von dpspi in die spektrochemische Reihe wird diskutiert. Der nephelauxetische Effekt ist außerordentlich groß. Die PSe-Valenzschwingungen der Diphenyldiselenophosphinato-Komplexe werden zugeordnet.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 3463-3474 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Disproportionation of Arylsemicarbazides1-Arylsemicarbazides, when activated with strong electron donating substituents in o- or p-position, are disproportionated by acids to form quinone imines and ureas. Dependent on their substitution the quinone imines are either hydrolized or they oxidize a second molecule of semicarbazide. This reaction shows specific acid catalysis and is of first order in H⊕ ions and semicarbazide.  -  Similarities to the disproportionation of hydrazobenzenes and to the osazone reaction are discussed.
    Notes: 1-Aryl-semicarbazide, die durch starke Elektronendonatoren in o- und p-Stellung des Arylrestes substituiert sind, werden durch Säuren zu Chinoniminen und Harnstoffen disproportioniert. In Abhängigkeit von ihrer Substitution werden die Chinonimine entweder hydrolysiert oder sie oxydieren ein zweites Molekül Arylsemicarbazid. Die Reaktion ist spezifisch säurekatalysiert und folgt in allen Fällen einem Gesetz 1. Ordnung bezüglich H⊕-Ionen und Substrat.  -  Analogien zur Disproportionierung von Hydrazobenzolen und zur Osazon-Reaktion werden aufgezeigt.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 3704-3710 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Substituted Succinic Acids, III. The Absolute Configuration of the 2-Methyl-3-ethylsuccinic AcidsOptically active threo- and erythro-2-methyl-3-ethylsuccinic acid (-2a and -3a) are reduced to (-)-2.3S-dimethylpentane (10) via the diols 8a and 9a. The bis-p-bromophenacyl esters of +2a, -2a, +3a and -3a are described.
    Notes: Optisch aktive threo- und erythro-2-Methyl-3-äthyl-bernsteinsäure (-2a und -3a) werden über die Diole 8a bzw. 9a zu (-)-2.3S-Dimethyl-pentan (10) reduziert. Die Bis-P-bromphenacylester von +2a, -2a, +3a und -3a werden beschrieben.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 3782-3793 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Chalkogen Compounds. Preparation, Electronic and Vibrational Spectra of Potassiumdiphenyldithioarsinate and Diphenyldithioarsinato ComplexesThe diphenyldithioarsinato complexes of NiII, CoII, ZnII, InIII, CrIII and VIII were prepared from potassiumdiphenyldithioarsinate (3). 3 was prepared from the chloride 2 with KHS or from the arsinate 4 with H2S. The structure of the transition metal complexes was determined from electronic spectra and magnetic measurements. The position of the ligand in the spectro-chemical and nephelauxetical series is reported. The region for the v(AsS)-vibrations is between 400 and 500/cm.
    Notes: Die Diphenyldithioarsinato-Komplexe von NiII, CoII, ZnII, InIII, CrIII und VIII wurden aus Kaliumdiphenyldithioarsinat (3), dieses aus dem Chlorid 2 mit KHS oder aus dem Arsinat 4 mit H2S gewonnen. Aus Elektronenabsorptionsspektren und magnetischen Messungen konnte die Struktur der Übergangsmetallkomplexe abgeleitet werden. Der Ligand wird in die spektrochemische und nephelauxetische Reihe eingeordnet. Die v(AsS)-Valenzschwingungen liegen zwischen 400 und 500/cm.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 1815-1821 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Arsine Pentacarbonyl Complexes of Chromium(0), Molybdenum(0) and Tungsten(0)Preparation, i.r., 1H-n.m.r. and mass spectra of the diamagnetic, sublimable, yellow arsine pentacarbonyl complexes Cr(CO) 5AsH3, Mo(CO)5AsH3 and W(CO5AsH3 are reported. Properties of AsH3 as complex ligand are discussed and compared with those of PH3 and As(C6H5)3. Cr(CO)5SbH3 and Fe(CO) 4AsH3, confirmed only by mass spectrometry, are mentioned.
    Notes: Über Darstellung, IR- und 1H-NMR- sowie Massenspektren der diamagnetischen, sublimierbaren, gelben Arsin-pentacarbonyl-Komplexe Cr(CO)5ASH3, Mo(CO)5AsH3 und W (CO)5ASH3 wird berichtet. Die Eigenschaften von AsH3 als Komplexligand werden diskutiert und mit denen von PH3 und As (C6H5)3 verglichen. Das vorerst nur massenspektroskopisch gesicherte Cr(CO)5SbH3 und Fe(CO) 4AsH3 werden erwähnt.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 1922-1925 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrogen-Deuterium Exchange in S-Ethyl-S-methylsulfodiimide and in N.S.S-TrimethylsulfodiimideS-Ethyl-S-methylsulfodiimid, CH3(C2H5)S(NH)2 (1), and N.S.S-Trimethylsulfodiimide, (CH3)2S(NCH3)NH (2), exchange in D2O-solution the protons of the S-methyl groups with deuterium. The rates of reaction and activation energies were determined by n.m.r. spectroscopy. The S.S-dimethyl compound follows the Brönsted catalysis law.
    Notes: S-Äthyl-S-methyl-sulfodiimid, CH3(C2H5)S(NH)2 (1), und N.S.S-Trimethyl-sulfodiimid, (CH3)2S(NCH3)NH (2), tauschen in D2O ihre zum S-Atom α-ständigen Methylprotonen gegen Deuterium aus. Die Geschwindigkeitskonstanten und die Aktivierungsenergien werden mit Hilfe der Protonenresonanz bestimmt. Die S.S-Dimethylverbindung folgt dem Brönstedschen Katalysegesetz.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 671-673 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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