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Poly(β-amino acid)s. IV. Synthesis and conformational properties of poly(α-isobutyl-L-aspartate)
Authors:Heimei Yuki  Yoshio Okamoto  Yutaka Taketani  Tetsuo Tsubota  Yoshizo Marubayashi
Abstract:Poly(α-isobutyl-L -aspartate) was prepared by the polycondensation reaction of p-nitrophenyl ester of α-isobutyl-L -aspartate and the conformation of the poly(β-amino acid) was investigated by X-ray diffraction, polarized infrared, circular dichroism (CD), optical rotatory dispersion (ORD), and NMR spectroscopy. α-Isobutyl β-p-nitrophenyl-L -aspartate hydrochloride and hydrobromide were used as monomers and dimethylformamide, chloroform, and chlorobenzene, as solvents. A high-molecular-weight polymer with [η] 1.0 dl/g (dichloroacetic acid, 25°C) was formed in the polymerization of the hydrochloride in chloroform at 25°C. The X-ray diagram and polarized infrared spectrum of the stretched polymer film obtained from a chloroform solution suggested a cross-β-form as the most probable structure in the solid state. The CD spectra of the polymer in a 2,2,2-trifluoroethanol (TFE) solution and its film cast from the solution showed a peak at 205 nm and a trough at 190 nm which were assigned to a β-structure. The polymer was associated in chloroform. The NMR and ORD spectra in chloroform were similar to those in TFE, which suggests that the polymer also exists in the β-structure in chloroform. The addition of small amounts of dichloroacetic acid and sulfuric acid to chloroform and TFE solutions, respectively, destroyed the β-structure. A random copolymer of α-isobutyl-L -aspartate with β-alanine was also prepared by polycondensation reaction. The copolymer apparently did not form an ordered structure in the solid state or in solution.
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