Highly Isoselective Coordination Polymerization of ortho-Methoxystyrene with β-Diketiminato Rare-Earth-Metal Precursors

被引:135
|
作者
Liu, Dongtao [1 ]
Yao, Changguang [1 ]
Wang, Rong [2 ]
Wang, Meiyan [1 ,3 ]
Wang, Zichuan [1 ]
Wu, Chunji [1 ]
Lin, Fei [1 ]
Li, Shihui [1 ]
Wan, Xinhua [2 ]
Cui, Dongmei [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys, Coll Chem & Mol Engn,Minist Educ, Beijing 100871, Peoples R China
[3] Jilin Univ, Inst Theoret Chem, Changchun 130022, Peoples R China
关键词
beta-diketiminate ligand; density functional calculations; isoselective polymerization; ortho-methoxystyrene; rare-earth metal complex; SYNDIOTACTIC POLYSTYRENE; STYRENE POLYMERIZATION; ALPHA-OLEFINS; STEREOSPECIFIC POLYMERIZATION; INSERTION POLYMERIZATION; FUNCTIONALIZED OLEFINS; VINYL MONOMERS; COPOLYMERIZATION; COMPLEXES; CATALYSTS;
D O I
10.1002/anie.201412166
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stereoselective coordination/insertion polymerization of the polar ortho-methoxystyrene has been achieved for the first time by using the cationic beta-diketiminato rare-earth-metal species. High activity and excellent isoselectivity (mmmm>99%) were acheived. The unmasked Lewis-basic methoxy group does not poison the Lewis-acidic metal center, but instead activates the polymerization through sigma-pi chelation to the active species together with the vinyl group, thus lower the coordination and activation energies as compared with those of styrene derivatives lacking the methoxy group.
引用
收藏
页码:5205 / 5209
页数:5
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