Abstract: The present invention provides an aromatic polyester which is substantially free from the occurrence of coloration and retains significantly high transparency even after being thermally processed at high temperature and which has high flowability. The aromatic polyester contains a polyhydric phenol residue and a residue of any one of aromatic polycarboxylic acid, halide thereof, and anhydride thereof, and terminals of the aromatic polyester have a structure represented by the formula —C(O)—R. The aromatic polyester has an end-capping rate of 90% or higher and a weight average molecular weight (Mw) ranging from 3,000 to 1,000,000.

Abstract: The invention provides an optically active polymer which is a product obtained by polymerizing a chiral alkoxy-substituted phenylacetylene such as p-(2-methylbutoxy)phenylacetylene, of which the 2-methylbutoxy group has chirality, in an organic solvent such as triethylamine in the presence of a rhodium complex compound as a polymerization catalyst. The optically active polymer exhibits a much larger optical rotation than the monomeric compound per se and is colored in different colors of, e.g., yellow and black, depending on the organic solvent used for polymerization. The yellow polymer turns to black by exposure to the vapor of a specific organic solvent such as chloroform and returns to yellow by re-precipitation from a chloroform solution with addition of methyl alcohol as a precipitant.

Abstract: The invention provides an optically active polymer which is a product obtained by polymerizing a chiral alkoxy-substituted phenylacetylene such as p-(2-methylbutoxy)phenylacetylene, of which the 2-methylbutoxy group has chirality, in an organic solvent such as triethylamine in the presence of a rhodium complex compound as a polymerization catalyst. The optically active polymer exhibits a much larger optical rotation than the monomeric compound per se and is colored in different colors of, e.g., yellow and black, depending on the organic solvent used for polymerization. The yellow polymer turns to black by exposure to the vapor of a specific organic solvent such as chloroform and returns to yellow by re-precipitation from a chloroform solution with addition of methyl alcohol as a precipitant.