化学
异戊二烯
钳子运动
钳形配体
聚合
配体(生物化学)
催化作用
金属
立体选择性
药物化学
核磁共振波谱
高分子化学
立体化学
有机化学
共聚物
生物化学
聚合物
受体
作者
Chenghao Chu,Xiangrui Wang,Jiang-Sheng Huang,Zeming Huang,Qinghai Li,Fenhua Wang
标识
DOI:10.1016/j.molstruc.2023.135498
摘要
Rare-earth metal dialkyl complexes [1-CH2N(CH3)2–3-CH2CH2N(CH3)2C8H4N]RE(CH2SiMe3)2 (RE = 1-Y, 2-Er, 3-Yb and 4-Lu) were synthesized by the well-designed indolyl-based proligand 1-CH2N(CH3)2–3-CH2CH2N(CH3)2C8H4NH with rare-earth metal trialkyl complexes (RE(CH2SiMe3)2(THF)2) underwent direct alkane elimination. Single-crystal X-ray analyses and the NMR spectroscopy revealed these dialkyl complexes were analogous mononuclear NCN-pincer geometry via CH activation of 2-sp2 indole. Employing these complexes, upon activation by aluminum alkyls and borate, initiated isoprene polymerization with high conversion and high stereoselectivity (98% conversion of 2000 equivalent of isoprene, 1,4-cis polymers up to 91.5%).
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