DEHYDROHOMOPOLYMERIZATION AND DEHYDROCOPOLYMERIZATION OF NEW ALKYLSILANES - SYNTHESIS OF POLY(3-ARYL-1-SILABUTANES)

Citation
Hg. Woo et al., DEHYDROHOMOPOLYMERIZATION AND DEHYDROCOPOLYMERIZATION OF NEW ALKYLSILANES - SYNTHESIS OF POLY(3-ARYL-1-SILABUTANES), Organometallics, 14(5), 1995, pp. 2415-2421
Citations number
35
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
14
Issue
5
Year of publication
1995
Pages
2415 - 2421
Database
ISI
SICI code
0276-7333(1995)14:5<2415:DADONA>2.0.ZU;2-V
Abstract
3-Aryl-1-silabutanes such as 3-phenyl-1-silabutane (1), 3-tolyl-1-sila butane (2), 3-(2,5-dimethylphenyl)-1-silabutane (3), 3-chlorophenyl-1- silabutane (4), 3-(chloro-p-tolyl)-1-silabutane (5), 3-(phenoxyphenyl) -1-silabutane (6), 3-naphthyl-1-silabutane (7), and bis(1-sila-3-butyl )benzene (8) were prepared in 62-98% yields by reduction of the corres ponding 3-aryl-1,1-dichloro-1-silabutanes with LiAlH4. The dehydrohomo polymerization and dehydrocopolymerization of the monomer silanes were carried out with the Cp(2)MCl(2)/Red-Al (M = Ti, Hf) combined catalys t system. The molecular weight of the polymers produced ranged from 60 0 to 1300 (vs polystyrene) with degree of polymerization (DP) equal to 3-16 and with polydispersity index (PDI) equal to 1.1-3.8. A set of t he monomer silanes dehydrocoupled to produce a copolymer. The polymeri zation of bis(silabutyl)benzene (8) seemed to initially produce a low molecular weight of polymer, which then underwent an extensive cross-l inking reaction of backbone Si-H bonds, leading to insoluble polymer.