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  • 1975-1979  (6)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 108 (1977), S. 1019-1025 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Oxozirconium(IV) alkoxides of the type ZrO(OR)2·ROH and ZrOCl(OR)·2 ROH, where R is methyl, ethyl, and isopropyl, and ZrO(OCMe 3)2·0.5Me 3COH and ZrOCl(OCMe 3)·1.5Me 3COH have been prepared by the reaction of dichloroxozirconium(IV)-2-acetic acid with corresponding alcohols in the presence of appropriate amounts of piperidine. The alkoxides have been isolated and characterised through infrared, thermal and conductance studies.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 106 (1975), S. 1375-1380 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The Schiff base salicylideneamino-o-methylthiobenzene (I), CH3S−C6H4−N=CH−C6H4−OH (SMeNOH), has been synthesized and its complexes of the type CuX(SMeNO) whereX=Cl, Br, NO3, CNS, and ClO4, CuX′(SMeNOH) whereX′=SO4 and (BF4)2, NiX″ 2(SMeNOH) whereX″=Cl and Br, NiNO3(SMeNO) andM(SMeNO) 2 whereM=Cu, Ni and Co, have been prepared and characterised through infrared, magnetic moment and conductance measurements.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 710-722 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Derivatives of Hydrazine, 51) Preparation and Some Properties of Trimethylsilylated, -germylated, and -stannylated TosylhydrazinesWith the exception of TosN2H(SnMe3)2, all tosylhydrazines TosN2Hm(E′Me3)n(E″Me3)0-(E‴Me3)p(E′, E″, E‴= So, Ge, Sn; m + n + o + p = 3) have been synthesized and characterized. These were prepared mostly by silylation, germylation, or stannylation of tosylhydrazine, TosN2H3, with chlorides Me3ECl or amines Me3ENR2, and, in a few cases, by tosylation of hydrazines N2H2(EMe3)2 and N2H2(EMe3)3 with tosyl chloride. Amines Me3ENR2 react with these newly synthesized tosylhydrazines by an exchange of hydrogen or of E′Me3 for EMe3. The hydrazides TosN2Li(SiMe3)(EMe3), obtained by the reaction of LiN(SiMe3)2 with TosN2Li(SiMe3)(EMe3) (E=Si, Ge) decompose on heating into TosLi and the azo-compounds Me3Si—N=N—EMe3.
    Notes: Mit Ausnahme von TosN2H(SnMe3)2 konnten alle Tosylhydrazine TosN2Hm(E′Me3)n(E″Me3)0-(E‴Me3)p(E′, E″, E‴=Si, Ge, Sn; m + n + o + p = 3) synthetisiert und charakterisiert werden. Ihre Darstellung erfolgte in den meisten Fällen durch Silylierung, Germylierung oder Stannylierung von Tosylhydrazin, TosN2H3, mit Chloriden Me3 ECl oder Aminen Me3ENR2, in einigen Fällen durch Tosylierung von Hydrazinen N2H2(EMe3)2 und N2H(EMe3)3 mit Tosylchlorid. Amine Me3ENR2 reagieren mit den neu dargestellten Verbindungen unter Austausch sowohl von Wasserstoff als auch von E′Me3 gegen EMe3. Die aus TosN2H)SiMe3)(EMe3) (E=Si, Ge) mittels LiN(SiMe3)2 erhältlichen Hydrazide TosN2Li(SiMe3)(EMe3) liefern bei höheren Temperaturen unter TosLi-Abspaltung die Azoverbindungen Me3Si—N=N—EMe3.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 2718-2729 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tetrasubstituted Tetrazenes (Me3E)2N—N = N—N(EMe3)2 (E = Si, Ge, Sn): Preparation, Characterization, and DecompositionTetrakis(trimethylsilyl)tetrazene (1) is formed in almost quantitative yield by the catalytic dimerization of bis(trimethylsilyl)diazene with silicon tetrafluoride. The tetrazene N4H4, obtained as a result of protolysis of 1 with trifluoroacetic acid, is converted quantitatively into tetrakis-(trimethylgermyl)tetrazene (2) and tetrakis(trimethylstannyl)tetrazene (3) by Me3ENR2 (E = Ge, Sn). The colourless, crystalline tetrazenes 1-3 have 2-tetrazene constitution, trans-configuration and planar conformation of E4N4-skeleton. The thermolysis of the tetrazenes above 100-150°C occurs under nitrogen evolution mainly into (Me3Si)2NH for 1, (Me3Ge)4N2 for 2, and a mixture of (Me3Sn)3N and (Me3Sn)2 for 3. The tetrazenes 1 and 2 photolyse easily to (Me3E)3N and Me3EN3, whereas 3 reacts by photolysis to form (Me3Sn)3N, (Me3Sn)2, and N2.
    Notes: Tetrakis(trimethylsilyl)tetrazen (1) entsteht in fast quantitativer Ausbeute durch katalytische Dimerisierung von Bis(trimethylsilyl)diazen mit Siliciumtetrafluorid. Das aus 1 durch Protolyse mit Trifluoressigsäure erhältliche Tetrazen N4H4 läßt sich mittels Me3ENR2 (E = Ge, Sn) quantitativ in Tetrakis(trimethylgermyl)tetrazen (2) sowie Tetrakis(trimethylstannyl)tetrazen (3) umwandeln. Die farblosen, kristallisierten Tetrazene 1-3 haben 2-Tetrazen-Konstitution, trans-Konfiguration sowie planare Konformation des E4N4-Gerüsts. Die Thermolyse der Tetrazene oberhalb von 100-150°C führt unter Stickstoffentwicklung hauptsächlich zu (Me3Si)2NH im Falle von 1, (Me3Ge)4N2 im Falle von 2 sowie einem Gemisch von (Me3Sn)3N und (Me3Sn)2 im Falle von 3. Die Tetrazene 1 und 2 photolysieren rasch in (Me3E)3N und Me3EN3, während 3 photolytisch in (Me3Sn)3N, (Me3Sn)2 und N2 übergeht.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 88 (1976), S. 257-258 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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