Azopolyesters with Intrinsic Crystallinity and Photoswitchable Reversible Solid‐to‐Liquid Transitions

Author:

Li Jie12,Zhang Qiu‐Yu2,Lu Xiao‐Bing1ORCID

Affiliation:

1. State Key Laboratory of Fine Chemicals Frontiers Science Center for Smart Materials Dalian University of Technology 2 Linggong Road 116024 Dalian China

2. School of Chemistry and Chemical Engineering Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology Northwestern Polytechnical University 710072 Xi'an China

Abstract

AbstractHerein, we introduce a variety of azopolyesters (azobenzene‐based polyesters) with remarkable intrinsic crystallinity and photoinduced reversible solid‐to‐liquid transition abilities from copolymerization of azobenzene‐based epoxides with cyclic anhydrides. The length of the soft alkyl side‐chain inlaid with azobenzenes and stereoregularity of main‐chain of azopolymers have tremendous effects on crystallization properties of the resulting polyesters with melting temperature (Tm) in the range of 51–251 °C. Moreover, some of azopolyesters possess excellently photoinduced reversible solid‐to‐liquid transition performance thanks to trans‐cis photoisomerization of azobenzenes. Trans‐azopolyesters are yellow solids with Tms or glass transition temperatures (Tgs) above room temperature, whereas cis‐polymers are red liquids with Tgs below −20 °C. These azopolyesters could be applied as novel light‐switchable adhesives for quartz/quartz, wood/wood and quartz/wood adhesion, with the strength in the range of 0.73–0.89 MPa for trans‐polymers. Conversely, the adhesion strength of liquefied cis‐azopolyesters generated from the irradiation of trans‐polymers by UV light was about 0.1 MPa, which shows light enable to control the adhesion process with high spatiotemporal resolution.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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