SYNTHESIS AND PROPERTIES OF POLY(DIPHENYLACETYLENES) HAVING ALIPHATICPARA-SUBSTITUENTS

Citation
H. Kouzai et al., SYNTHESIS AND PROPERTIES OF POLY(DIPHENYLACETYLENES) HAVING ALIPHATICPARA-SUBSTITUENTS, Journal of polymer science. Part A, Polymer chemistry, 32(13), 1994, pp. 2523-2530
Citations number
14
Categorie Soggetti
Polymer Sciences
ISSN journal
0887624X
Volume
32
Issue
13
Year of publication
1994
Pages
2523 - 2530
Database
ISI
SICI code
0887-624X(1994)32:13<2523:SAPOPH>2.0.ZU;2-V
Abstract
1-(p-t-Butylphenyl)-2-phenylacetylene and 1-(p-n-butylphenyl) -2-pheny lacetylene were polymerized in catalytic systems based on TaCl5 to giv e new polymers in high yields. These monomers were more reactive than diphenylacetylene (DPA) in copolymerization. Unlike poly(DPA), the pre sent polymers were soluble in toluene, CHCl3, etc. owing to the high c onfigurational entropy induced by the para-substituents. Their relativ e weight-average molecular weights determined by GPC were in the range of 6 X 10(5)-36 X 10(5), and films could be obtained by solution cast ing. These polymers were fairly thermally stable, as seen from their h igh onset temperatures (320-380 degrees C) of weight loss in TGA in ai r. The oxygen permeability coefficient of the polymer with t-Bu group was 1100 barrers, the highest among those of all the hydrocarbon polym ers. (C) 1994 John Wiley & Sons, Inc.