Combining alkali metals and zinc to harness heterometallic cooperativity in cyclic ester ring-opening polymerisation

被引:25
作者
Gruszka, Weronika [1 ]
Lykkeberg, Anna [1 ]
Nichol, Gary S. [1 ]
Shaver, Michael P. [2 ]
Buchard, Antoine [3 ]
Garden, Jennifer A. [1 ]
机构
[1] Univ Edinburgh, EaStCHEM Sch Chem, Edinburgh EH9 3FJ, Midlothian, Scotland
[2] Univ Manchester, Sch Nat Sci, Dept Mat, Henry Royce Inst, Manchester M13 9PL, Lancs, England
[3] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
MOLECULAR-STRUCTURE; LIGAND SYNTHESIS; RAC-LACTIDE; CATALYSTS; COMPLEXES; ALUMINUM; POLYLACTIDES;
D O I
10.1039/d0sc04705h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterometallic cooperativity is an emerging strategy to elevate polymerisation catalyst performance. Here, we report the first heterotrimetallic Na/Zn-2 and K/Zn-2 complexes supported by a ProPhenol ligand, which deliver "best of both" in cyclic ester ring-opening polymerisation, combining the outstanding activity (Na/K) and good control (Zn-2) of homometallic analogues. Detailed NMR studies and density-functional theory calculations suggest that the Na/Zn-2 and K/Zn-2 complexes retain their heterometallic structures in the solution-state. To the best of our knowledge, the K/Zn-2 analogue is the most active heterometallic catalyst reported for rac-lactide polymerisation (k(obs) = 1.7 x 10(-2) s(-1)), giving activities five times faster than the Na/Zn-2 complex. These versatile catalysts also display outstanding performance in epsilon-caprolatone and delta-valerolactone ring-opening polymerisation. These studies provide underpinning methodologies for future heterometallic polymerisation catalyst design, both in cyclic ester polymerisation and other ring-opening (co)polymerisation reactions.
引用
收藏
页码:11785 / 11790
页数:6
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