One chain of conducting and polar polymers was isolated by using inclusion in the cavity of cyclodextrins (CD's) and intercalation between the crystal lattices of tris(2, 3-naphthylenedioxy)cyclotriphosphazene (NapCP). Optical, electrochemical, and thermal properties of the isolated one chain of the polymers were considerably different from those of polymers in bulks. Water-insoluble poly(thiophene-2, 5-diyl) (PTh), poly(3-methylthiophene-2, 5-diyl), and poly(pyridine 2, 5-diyl) (PPy) became water-soluble by inclusion in β-CD. The aqueous solution of PPy included in β-CD showed an absorption peak at a longer wavelength (434 nm) than PPy in formic acid by 50 nm and a higher quantum yield of photoluminescence (Φ=41%) than PPy in formic acid (Φ=4%). Standing an
N-methyl-2-pyrrolidone solution containing emeraldine base form of polyaniline (PANI) and NapCP caused intercalation of PANI in the channels generated by self-assembling of NapCP to give an inclusion adduct. Thermal stability of PANI was improved by intercalation in the channel. Polar polymers such as polybenzimidazole and polyurethane form interchain hydrogen bonding, which strongly effects on thermal properties of the polymers. Inclusion of the polymers into CDs disturbed the interchain hydrogen bonding, which resulted in lowering of glass transition temperatures of the polymers.
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