Synthesis of pyrrolidinyl-ethylene fluorenyl rare-earth metal complexes and catalysis for 2-vinylpyridine polymerization

被引:2
|
作者
Wang, Yinjun [1 ]
Jiang, Hao [1 ]
Wang, Huifei [1 ]
Mou, Zehuai [1 ]
机构
[1] Ningbo Univ, Sch Mat Sci & Chem Engn, Key Lab Adv Mass Spectrometry & Mol Anal Zhejiang, Ningbo 315211, Peoples R China
基金
中国国家自然科学基金;
关键词
Rare-earth metal; Constrained -geometry complex; 2-Vinylpyridine; Stereoselective polymerization; SYNDIOSELECTIVE COORDINATION (CO)POLYMERIZATION; STYRENE; COPOLYMERIZATION; ISOPRENE; LIGANDS;
D O I
10.1016/j.jre.2022.02.018
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The metathesis reaction between pyrrolidinyl-ethylene fluorenyl lithium salts with in situ prepared cationic rare-earth metal dialkyl species [Ln(CH2SiMe3)2(THF)x][BPh4] afford efficiently the corre-sponding constrained-geometry complexes L1Ln(CH2SiMe3)2 (L1 = FluCH2CH2NC4H8, Ln = Y (1a), Lu (1b), Sc (1c)) and L2Ln(CH2SiMe3)2 (L2 = (2,7-di-tert-butyl)FluCH2CH2NC4H8, Ln = Y (2a), Lu (2b), Sc (2c)) in good yields. All these complexes were characterized by NMR spectroscopy, and the solid-state molecular structure of yttrium complex 1a was defined with single-crystal X-ray diffraction analysis. The catalytic performance of these complexes towards 2-vinylpyridine polymerization was investigated, where these complexes alone can efficiently promote the polymerization of 2-vinylpyridine giving isotactic poly(2-vinylpyridine). Upon the activation with [Ph3C][B(C6F5)4], the yttrium and lutetium complexes also afford isotactic poly(2-vinylpyridine), while the scandium complexes produce syndiotactic poly(2-vinylpyridine).(c) 2022 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:381 / 387
页数:7
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