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Updated: Mar 18, 2026

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Photoswitchable ring-opening polymerization of lactide catalyzed by azobenzene-based thiourea
Zhongran Dai1, Yaqin Cui1, Changjuan Chen1
1State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou 730000, Gansu, People's Republic of China. wujc@lzu.edu.cn.
Abstract:
The reactivity of a catalytic polymerization system using photoresponsive azobenzene-based thiourea/PMDETA as a catalyst could be switched between slow and fast states by alternating exposure to UV and ambient light, because the active site of azobenzene thiourea is blocked via intramolecular hydrogen bonding when the azobenzene thiourea transfers from the E isomer to the Z isomer under UV irradiation.
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