战术性
聚丙烯
聚合物
单体
催化作用
高分子化学
微观结构
碳-13核磁共振
聚合
表征(材料科学)
化学
纳塔
高分子科学
材料科学
化学工程
结晶学
有机化学
纳米技术
工程类
作者
Giuseppe Antinucci,Antonio Vittoria,Roberta Cipullo,Vincenzo Busico
出处
期刊:Macromolecules
[American Chemical Society]
日期:2020-05-05
卷期号:53 (10): 3789-3795
被引量:20
标识
DOI:10.1021/acs.macromol.0c00433
摘要
Isotactic polypropylene (i-PP) is mainly produced with heterogeneous Ziegler–Natta (ZN) catalyst systems. Direct structural information on the active species is very difficult to achieve; as a matter of fact, the 13C NMR microstructure of the polymer has long been used as an indirect "fingerprint". For a long time, however, the intrinsically poor sensitivity of natural abundance 13C NMR spectroscopy hampered a complete evaluation of the microstructure, and many rare albeit important details escaped detection with standard tools and methods. The most prominent case is that of the regiodefects, which are specially important because they dictate ZN catalyst response to molecular hydrogen used as a chain transfer agent. In recent papers we have reported on the quantification of regioirregular 2,1 units in ZN i-PP by means of high-temperature cryoprobe 13C NMR. Here we shift the focus onto the stereochemical environment of such units, which was highlighted by comparing the spectra of suitable ZN PP fractions with those of model PP samples made with molecular catalysts of different structures and symmetries. The results lend support to our three-site model of ZN catalytic species, originally based on the stereochemistry of regioregular PP chains/blocks.
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