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  • mesophases  (2)
  • Bissilylamines  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Some recent developments in polysilane chemistry (1992)
    Springer
    Journal of inorganic and organometallic polymers and materials 2 (1992), S. 29-45 
    Details
    ISSN: 1572-8870
    Keywords: Polysilenes ; polysilanes ; liquid crystals ; mesophases ; birefringence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract (I) Ordered and disordered polysilane copolymers: Condensation of ClSiMe2Si(n-Hex)2SiMe2Cl with Na/K in toluene at 90°C produced a polymer with a strongly bimodal molecular weight distribution. The high-M w and low-M w portions were separated by fractional precipitation with 2-propanol, and the properties of the two fractions were investigated.29Si-NMR spectra show that the low-M w fraction is fully ordered but the high-M w fraction is randomized. (II) Liquid crystalline polysilanes: Condensation ofn-Bu(n-Hex)SiCl2 with Na in toluene led to a homopolymer which is a rubbery solid at 25°C. The polymer undergoes a second-order transition at −45°C and a first-order (melt) transition at −20°C. X-ray diffraction shows that the polymer has the same structure, a columnar hexagonal lattice, in all three phases; from −20 to 〉200°C, it exists in a columnar liquid crystalline mesophase. Similar hexagonal mesophases were observed at 25°C for the family of copolymers, (n-Hex2Si) n (Alk2Si) m , Alk =n-Pentyl,n-Bu,n-Pr, Et, Me.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00696534
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  • 2
    Electronic Resource
    Electronic Resource
    Ethynylene-disilanylene copolymers (1991)
    Springer
    Journal of inorganic and organometallic polymers and materials 1 (1991), S. 545-565 
    Details
    ISSN: 1572-8870
    Keywords: Polysilanes ; sigma-pi conjugation ; mesophases ; polymer crystals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Polymers of structure (SiR2SiR2-C ≡ C-SiR2′SiR2′-C ≡ C) n , in which ethynylene units alternate with disilylene units, have been prepared by two routes: (a) condensation of dichlorodisilanes with dilithium derivatives of 1,2-diethynyldisilanes and (b) ring-opening polymerization of strained cyclic disilanylene-acetylnes, (SiR2SiR2C ≡ C)2. The polymers display UV absorption near 240 nm indicative of σ − π conjugation between the Si2 and the C ≡ C moieties. Polymers with R=R′=n-Bu or R=n-Bu, R′=Ph, undergo solid-state transitions to form liquid crystalline mesophases resembling those observed for many poly(silylenes). Single crystals were obtained for the polymer with R=R′=CH3, by precipitation from dilute cyclohexane solution. The solid-state properties and structures of this family of polymers are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00683516
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  • 3
    Electronic Resource
    Electronic Resource
    Synthetic and Structural Studies of 1-Sila-2,5-diaryltetrazenes (1997)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1579-1583 
    Details
    ISSN: 0009-2940
    Keywords: Silatetrazenes ; Nitrogen-silicon ring systems ; Bissilylamines ; Silicon-29 solid state NMR ; Aryl azides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction between aryl azides and lithiated aryl amines leads to tetrazenes 3 and 9 which contain a chain of four nitrogen atoms. Reaction with different halosilanes gives the cyclic silatetrazenes 10, 12, and 15 where substitutents on the silicon vary form alkyl to hydrogen and chlorine atoms. The structures of 10, 12, and 15 in the solid state are reported. Variation of the solvent and the Lewis acidity of the halosilane influence the ratio of silatetrazene to side products, bissilyated amines. These effects are studied for different halosilanes.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19971301105
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