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  • 1980-1984  (3)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 40 (1984), S. 871-873 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Functional Siloxanes and Cyclotetrasiloxanes - Molecular Structure of a CycloboratrisiloxaneLithium salts of di-tert-butyl-fluorosilanol and -silandiol react with fluorosilanes to give 1,3-di- (1, 2), 1,3,5-tri- (3, 4), and 1,3,5,7,9-pentasiloxanes (5). Reactions of the dilithium salt of the silandiol with SiF4 and CH3SiF3 lead to the formation of fluorofunctional cyclo-1,3,5,7-tetrasiloxanes (6, 7). The cyclotetra-siloxane 8 is obtained by thermal LiF elimination from 1,1-difluoro-1,3-disiloxane-3-ol (2). The eight-membered ring systems 9 and 10 are formed in the reaction of dilithiated 1,3,5-trisiloxane-1,5-diol with SiF4 (9) and BF3 (10). The crystal structure of the cyclo-1-bora-3,5,7-trisiloxane 10 is reported and discussed.
    Notes: Lithiumsalze des Di-tert-butylfluorsilanols und -silandiols reagieren mit Fluorsilanen zu fluorfunktionellen 1,3-Di- (1, 2), 1,3,5-Tri- (3, 4) und 1,3,5,7,9-Pentasiloxanen (5). Der Einsatz des Dilithiumsalzes des Silandiols führt in der Reaktion mit SiF4 und CH3SiF3 zur Bildung fluorfunktioneller Cyclo-1,3,5,7-tetrasiloxane (6, 7). Das Cyclotetrasiloxan 8 wird durch thermische LiF-Abspaltung aus 1,1-Difluor-1,3-disiloxan-3-ol (2) erhalten. Die achtgliedrigen Ring-systeme 9 und 10 entstehen in der Reaktion des dilithiierten 1,3,5-Trisiloxan-1,5-diols mit SiF4 (9) und BF3 (10). Die Kristallstruktur des Cyclo-1-bora-3,5,7-trisiloxans 10 wird vorgestellt und diskutiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 514 (1984), S. 49-60 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Poly- and Spirocyclic Silylhydrazones  -  Synthesis and Molecular StructuresBulky aminotrifluorosilanes react with lithiated dimethylketone-hydrazone to give 1,2-diaza-3-sila-5-cyclopentenes  -  DSCP  -  (1, 2). The 4-silylated (3-5, 8-15) and siloxysilyl-substituted (17, 18) rings eliminate no halosilane or siloxane thermally. Lithiated 2 dimerises with LiF elimination to give the (2+2)cycloadduct of a 1,2-diaza-3-sila-3,5-cyclopentadiene (6). Lithiated DSCP reacts with MeSiF2N(CMe3)SiMe2CMe3 via a nucleophilic 1,3-methanide ion migration to form LiF and the spirocyclic compound 18. A compound with spirocyclic silicon (21) is formed in the reaction of bis(1,2-diaza-3-sila-5-cyclopenten-4-yl)difluorosilane (19) and the lithium salt of dimethyl-ketone-tert-butylhydrazone. The crystal structures of 6 and 21 are reported.
    Notes: Voluminöse Aminotrifluorsilane reagieren mit lithiiertem Dimethylketon-hydrazon zu 1,2-Diaza-3-sila-5-cyclopentenen  -  DSCP  -  (1, 2). In 4-Stellung silyl- (3-5, 8-15) und siloxysilylsubstituierte (17, 18) Ringe spalten thermisch kein Halogensilan oder Siloxan ab. Lithiiertes 2 dimerisiert unter LiF-Abspaltung zum (2+2)Cycloaddukt eines 1,2-Diaza-3-sila-3,5-cyclopentadiens (6). Lithiiertes DSCP reagiert mit MeSiF2N(CMe3)SiMe2CMe3 unter LiF-Ab-spaltung und nucleophiler 1,3-Methanidionen-Wanderung zum Spirocyclus 18. Eine Verbindung mit spirocyclischem Silicium (21) entsteht in der Reaktion des Bis-(1,2-diaza-3-sila-5-cyclopenten-4-yl)-difluorsilans (19) mit dem Lithiumsalz des Dimethylketon-tert-butyl-hydrazon. Die Kristallstrukturen von 6 und 21 werden mitgeteilt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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