FUNCTIONAL POLYSILANES .4. DUPLICATION BY REDUCTION OF CHLOROSILANES BY LITHIUM FOR THE SYNTHESIS OF MEGA-BIS(TRIMETHYLSILYL)OLIGO(METHYLPHENYLSILANE)S - PARASITE SILYLATION REACTIONS OF PHENYL NUCLEI
D. Reyx et al., FUNCTIONAL POLYSILANES .4. DUPLICATION BY REDUCTION OF CHLOROSILANES BY LITHIUM FOR THE SYNTHESIS OF MEGA-BIS(TRIMETHYLSILYL)OLIGO(METHYLPHENYLSILANE)S - PARASITE SILYLATION REACTIONS OF PHENYL NUCLEI, Macromolecular chemistry and physics, 196(1), 1995, pp. 149-166
The coupling of dichloromethylphenylsilane (1) with chlorotrimethylsil
ane (2) by lithium is considered for the synthesis of low-molecular-we
ight organosilane polymers 3 and for the preparation of heptamethylphe
nyl-2-trisilane (3 a) and octamethyldiphenyl-2,3-tetrasilane (3 b). Si
ze-exclusion chromatography, ultraviolet and infrared spectroscopies a
nd nuclear magnetic resonance (H-1, C-13 and Si-29 NMR) analyses of th
e crude product 3 were performed and compared with those of 3 a and 3
b. According to the spectroscopic characteristics of rimethylsilyl)-3,
4,5,6-cyclohex-1-enyl-2-trisilane (4), and the observed silylation of
the trisilane 3 a when it is submitted to the action of a (CH3)(3)SiCl
/Li/tetrahydrofuran system, the silylation of the phenyl ring during t
he reductive condensation of the chlorosilanes is supported by NMR ide
ntification of 4-like structures.