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Copolymerization of 1‐(trimethylsilyl)‐1‐propyne with disubstituted hydrocarbon acetylenes

1988; Wiley; Volume: 26; Issue: 9 Linguagem: Inglês

10.1002/pola.1988.080260930

1099-0518

Toshiyuki Hamano, Toshio Masuda, Toshinobu Higashimura,

Organometallic Complex Synthesis and Catalysis

Abstract Copolymerization of 1‐(trimethylsilyl)‐1‐propyne (MeC ≡ CSiMe 3 ) with several aromatic and aliphatic disubstituted acetylenes (MeC ≡ CPh, n ‐BuC ≡ CPh, 2‐octyne, and 4‐octyne) were examined by using Ta and Nb catalysts. The TaCl 5 –Ph 3 Bi catalyst was effective in copolymerization with the aromatic acetylenes, whereas the NbCl 5 –Ph 3 Bi catalyst was preferable in copolymerization with the aliphatic acetylenes. The copolymerization products were not mixtures of homopolymers but copolymers. The relative reactivity of monomer tended to decrease with increasing steric effect of monomer: 2‐octyne > MeC ≡ CSiMe 3 > 4‐octyne > MeC ≡ CPh > n ‐BuC ≡ CPh. The copolymers of MeC ≡ CSiMe 3 with MeC ≡ CPh [copoly(TMSP/PP)s] had high molecular weight ( M w > 1 × 10 6 ), and provided thermally stable tough films. With increasing MeC ≡ CPh content of copoly(TMSP/PP), the oxygen permeability coefficient ( P ) decreased, while the separation factor ( P / P ) increased.