Chemoselective Polymerization of Polar Divinyl Monomers with Rare-Earth/Phosphine Lewis Pairs

被引:25
|
作者
Xu, Pengfei [1 ]
Wu, Lei [1 ]
Dong, Liqiu [1 ,2 ]
Xu, Xin [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China
[2] Suzhou Int Acad, BFSU, Suzhou 215200, Peoples R China
来源
MOLECULES | 2018年 / 23卷 / 02期
基金
中国国家自然科学基金;
关键词
Lewis pairs; rare-earth; phosphines; chemoselective polymerization; TRANSFER RADICAL POLYMERIZATION; POLY(ALLYL METHACRYLATE); ANIONIC-POLYMERIZATION; POLYMERS; COMPLEXES; CATALYSTS;
D O I
10.3390/molecules23020360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This work reports the chemoselective polymerization of polar divinyl monomers, including allyl methacrylate (AMA), vinyl methacrylate (VMA), and 4-vinylbenzyl methacrylate (VBMA), by using simple Lewis pairs comprised of homoleptic rare-earth (RE) aryloxide complexes RE(OAr)(3) (RE = Sc (1), Y (2), Sm (3), La (4), Ar = 2,6-tBu(2)C(6)H(3)) and phosphines PR3 (R = Ph, Cy, Et, Me). Catalytic activities of polymerizations relied heavily upon the cooperation of Lewis acid and Lewis base components. The produced polymers were soluble in common organic solvents and often had a narrow molecular weight distribution. A highly syndiotactic poly(allyl methacrylate) (PAMA) with rr similar to 88% could be obtained by the scandium complex 1/PEt3 pair at -30 degrees C. In the case of poly(4-vinylbenzyl methacrylate) (PVBMA), it could be post-functionalized with PhCH2SH. Mechanistic study, including the isolation of the zwitterionic active species and the end-group analysis, revealed that the frustrated Lewis pair (FLP)-type addition was the initiating step in the polymerization.
引用
收藏
页数:9
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