化学
钪
镥
丙交酯
钇
聚合
开环聚合
单体
高分子化学
金属
催化作用
镧
药物化学
有机化学
聚合物
氧化物
作者
Hui Liu,Fen You,Xiang Hu,Yanchen Huo,Xiaochao Shi
出处
期刊:Organometallics
[American Chemical Society]
日期:2022-11-10
卷期号:41 (23): 3645-3653
被引量:4
标识
DOI:10.1021/acs.organomet.2c00446
摘要
A family of rare-earth metal complexes bearing unsymmetrical diarylamido-[PNNox] pincer ligands with diverse chiral substituents were synthesized by utilizing direct alkane elimination. NMR and X-ray diffraction analyses revealed that the scandium and lutetium complexes were mononuclear, while the yttrium complexes were binuclear via the alkoxo bridges. All rare-earth metal complexes showed high catalytic activity for ring-opening polymerization (ROP) of rac-lactide, affording heteroselective polylactide (Pr up to 0.78). The yttrium complexes exhibited higher catalytic activity and higher heteroselectivity than the scandium and lutetium complexes. Especially, slight influence of the chiral substituents on the activity and heteroselectivity was observed in the catalytic systems. The kinetic study revealed that PMe–Y catalyzed the ROP of rac-lactide in a controlled manner and the polymerization proceeded with first-order dependence on both monomer and initiator concentrations.
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