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Updated: Sep 17, 2025

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Catalytic Ring-Opening Homopolymerization and Copolymerization of rac-Lactide and δ-Valerolactone Utilizing
Zeming Huang1, Xinlei Yi1, Rui Pan1
1Anhui Laboratory of Clean Catalytic Engineering, Anhui Laboratory of Functional Coordinated Complexes for Materials Chemistry and Application, College of Chemical and Environmental Engineering, Anhui Polytechnic University, Wuhu, Anhui 241000, P. R. China.
Abstract:
The copolymers of rac-lactide (rac-LA) and δ-valerolactone (δ-VL) can improve the properties of the individual polymers in terms of variable mechanical, thermal, permeability, and degradation properties. However, copolymerization of these two monomers catalyzed by metal catalysts faces challenges due to different activities of the intermediates in the propagation processes and lack of understanding the catalytic procedures to realize the copolymerization. Here, a series of novel indol-2-yl-based NNC pincer-type rare-earth metal dialkyl complexes (κ3NNC-L)RE(CH2SiMe3)2 (RE = Lu(1a), Yb(1b), Er(1c), Y(1d), Dy(1e)) (L = 1-(Me2NCH2CH2)-3-((Me2NCH2CH2)MeNCH2)-C8H4N) and carboryne-based rare-earth metallacycles (κ4NNCN-L)RE(η2-C2B10H10) (RE = Lu(2a), Yb(2b), Er(2c), Y(2d), Dy(2e)) were synthesized in good yields. These complexes exhibited high activity in homopolymerization of rac-LA and δ-VL. Notably, highly efficient block copolymerization procedures for the copolymerization of δ-VL and rac-LA initiated by metal complexes were for the first time described by controlling the sequence of feeding the two monomers in the presence of complexes 1 and 2, while the random copolymerization of δ-VL and rac-LA can also be realized by utilization of complexes 1 and 2 as catalysts.
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