Conformational studies of poly(β-phenethyl l-aspartate)

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Abstract

Poly(β-phenethyl L-aspartate) was synthesized and its conformational transitions in chloroform–dichloroacetic acid and chloroform–trifluoroacetic acid mixed solvents were examined by optical rotatory dispersion, circular dichroism and viscosity measurements. Poly(β-phenethyl L-aspartate), having a right-handed α-helical form in chloroform, undergoes a transition to a left-handed α-helical form by the addition of 2.0∧#x0025; dichloroacetic acid at 21°C. In the range of dichloroacetic acid content between 1.2&and#x0025; and 2.0&and#x0025;, the polymer exhibits a thermally-induced inversion of the helix sense from the right-handed to the left-handed. The transition temperature is dependent on the solvent composition. Furthermore, in the chloroform–trifluoroacetic acid system, the polymer exhibits both the helix-sense inversion and the helix–coil transition when the composition of the mixed solvent is varied. The thermally- and acid-induced inversions of the helix sense are discussed in terms of the change in the side chain conformation. © 1979, The Society of Polymer Science, Japan. All rights reserved.

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Toriumi, H., Saso, N., Yasumoto, Y., Sasaki, S., & Uematsu, I. (1979). Conformational studies of poly(β-phenethyl l-aspartate). Polymer Journal, 11(12), 977–981. https://doi.org/10.1295/polymj.11.977

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