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
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.