Synthesis of Rare Earth Metal Complexes Stabilized by Amine Bridged Bis(phenolato) Ligands and Their Performance in the Polymerization of rac-β-Butyrolactone

被引:0
|
作者
Shi, Yize [1 ]
Wang, Yanwei [1 ]
Yuan, Dan [1 ]
Yao, Yingming [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou Key Lab Macromol Design & Precis Synth,Jian, Suzhou 215123, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Rare-earth metal complexes; Amine-bridged bis(phenolato) ligands; rac-beta-butyrolactone; Ring-opening polymerization; Syndiotactic poly(3-hydroxybutyrate); RING-OPENING POLYMERIZATION; IMMORTAL POLYMERIZATION; ZINC CATALYSTS; YTTRIUM; LACTIDE; COPOLYMERIZATION; REACTIVITY;
D O I
10.1002/asia.202400820
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of rare earth alkoxides bearing amine-bridged bis(phenolato) ligands were synthesized through sequential reactions of RE(C5H5)3(THF) (RE = Y, Lu) or Nd[N(SiMe3)2]3 with bis(phenols) LH2 and CF3CH2OH. Complexes REL(OCH2CF3)(THF)n (1-6) bearing different aryl-substituents were obtained in good yields of 59-70 %. They were applied in the ring-opening polymerization (ROP) of rac-beta-butyrolactone (rac-BBL), which showed good activity (TOF up to 27,300 h-1), resulting in syndiotactically enriched poly(3-hydroxybutyrate) (PHB) (Pr up to 0.86) with narrow polydispersities (PDI <= 1.27). The yttrium complex 3 bearing bulky o-1,1-diphenylethyl substituents outperformed other complexes, suggesting that the smaller ionic radii of metal centers and bulky ortho substituents of ancillary ligands play crucial roles in controlling the activity and stereoselectivity in ROP of rac-BBL. Kinetics of the polymerization of rac-BBL initiated by complex 3 was investigated, which revealed first order dependences on the monomer and initiator concentrations, respectively.
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页数:7
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