锆
电泳剂
战斗
烯烃聚合
铪
催化作用
烯烃纤维
简单(哲学)
聚合
化学
材料科学
高分子化学
有机化学
哲学
历史
聚合物
古代史
认识论
作者
Antonio Vittoria,Georgy P. Goryunov,Vyatcheslav V. Izmer,Dmitry S. Kononovich,Oleg V. Samsonov,Francesco Zaccaria,Gaia Urciuoli,Peter H. M. Budzelaar,Vincenzo Busico,Alexander Z. Voskoboynikov,Dmitry V. Uborsky,Christian Ehm,Roberta Cipullo
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2021-08-06
卷期号:13 (16): 2621-2621
被引量:18
标识
DOI:10.3390/polym13162621
摘要
The performance of C2-symmetric ansa-hafnocene catalysts for isotactic polypropylene typically deteriorates at increasing temperature much faster than that of their zirconium analogues. Herein, we analyze in detail a set of five Hf/Zr metallocene pairs—including some of the latest generation catalysts—at medium- to high-polymerization temperature. Quantitative structure–activity relationship (QSAR) models for stereoselectivity, the ratio allyl/vinyl chain ends, and 2,1/3,1 misinsertions in the polymer indicate a strong dependence of polymerization performance on electrophilicity of the catalyst, which is a function of the ligand framework and the metal center. Based on this insight, the stronger performance decline of hafnocenes is ascribed to electrophilicity-dependent stabilization effects.
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