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Issue 19, 2015
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Photoinduced topological transformation of cyclized polylactides for switching the properties of homocrystals and stereocomplexes

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Abstract

Cyclized poly(L-lactide) and poly(D-lactide) (Mn ∼ 3 kDa) incorporating an o-nitrobenzyl group as a photocleavable linker were synthesized and photoirradiated for topological transformation to form photocleaved linear polylactides. By DSC, Tm of the cyclized stereocomplex (167 °C) decreased by more than 40 °C from that of the linear prepolymers (209 °C) despite their essentially identical molecular weights. Upon the photocleavage, the resulting linear stereocomplex showed almost the same Tm (211 °C) as that before the cyclization. The enthalpy of melting of crystals having an infinite thickness, i.e. ΔHm(100%), and the surface free energy (σe) were determined by the combination of WAXD, SAXS, and DSC. Both ΔHm(100%) and σe were considerably smaller for the cyclized polylactide homocrystals and stereocomplexes than those of the linear prepolymers and photocleaved products. These suggest that the absolute enthalpy of the melt state is lower, and the crystalline–amorphous interface is more stable for the cyclized polylactides arising from the topology.

Graphical abstract: Photoinduced topological transformation of cyclized polylactides for switching the properties of homocrystals and stereocomplexes

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Supplementary files

Article information


Submitted
03 Feb 2015
Accepted
03 Mar 2015
First published
04 Mar 2015

This article is Open Access

Polym. Chem., 2015,6, 3591-3600
Article type
Paper
Author version available

Photoinduced topological transformation of cyclized polylactides for switching the properties of homocrystals and stereocomplexes

N. Sugai, S. Asai, Y. Tezuka and T. Yamamoto, Polym. Chem., 2015, 6, 3591
DOI: 10.1039/C5PY00158G

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