Abstract

Two novel stereoregular poly(phenylacetylene)s bearing a phosphonic acid residue (poly-1) and its monoethyl ester (poly-2) as pendants were prepared by the polymerization of diethyl (4-ethynylphenyl)phosphonate followed by hydrolysis of the diethyl ester groups and polymerization of ethyl (4-ethynylphenyl)phosphonate, respectively. The polymers were found to form a predominantly one-handed helical conformation upon complexation with various chiral amines through noncovalent acid−base interactions in dimethyl sulfoxide (DMSO). The complexes exhibited an induced circular dichroism (ICD) in the UV−visible region of the polymer backbones. In particular, poly-2 is an induced helical polymer more sensitive to the chirality of amines than poly-1 and poly((4-carboxyphenyl)acetylene) and yields the same Cotton effect sign when complexed with chiral amines of the same absolute configuration. Moreover, the macromolecular helicity of poly-1 and poly-2 induced by chiral amines was “memorized” after the chiral amines w...

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