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布朗斯特酸催化的乙烯基醚的立体选择性聚合。

Brønsted Acid Catalyzed Stereoselective Polymerization of Vinyl Ethers.

机构信息

Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

出版信息

J Am Chem Soc. 2021 Oct 13;143(40):16388-16393. doi: 10.1021/jacs.1c08282. Epub 2021 Oct 1.

Abstract

Isotactic poly(vinyl ether)s (PVEs) have recently been identified as a new class of semicrystalline thermoplastics with a valuable combination of mechanical and interfacial properties. Currently, methods to synthesize isotactic PVEs are limited to strong Lewis acids that require a high catalyst loading and limit the accessible scope of monomer substrates for polymerization. Here, we demonstrate the first Brønsted acid catalyzed stereoselective polymerization of vinyl ethers. A single-component imidodiphosphorimidate catalyst exhibits a sufficiently low p to initiate vinyl ether polymerization and acts as a chiral conjugate base to direct the stereochemistry of monomer addition to the oxocarbenium ion reactive chain end. This Brønsted acid catalyzed stereoselective polymerization enabled an expanded substrate scope compared to previous methods, the use of chain transfer agents to lower catalyst loading, and the capability to recycle the catalyst for multiple polymerizations.

摘要

立构规整聚(乙烯基醚)(PVEs)最近被鉴定为一类新型的半结晶热塑性塑料,具有机械性能和界面性能的宝贵组合。目前,合成立构规整 PVEs 的方法仅限于强路易斯酸,需要高催化剂负载量,并限制了可用于聚合的单体底物的适用范围。在这里,我们展示了首例由 Brønsted 酸催化的立体选择性聚合乙烯基醚。单一组分的亚膦酰胺亚磷酸酯催化剂具有足够低的 pKa 值,可以引发乙烯基醚聚合,并作为手性共轭碱,将单体的立体化学加成到氧杂碳正离子活性链末端。与以前的方法相比,这种 Brønsted 酸催化的立体选择性聚合能够扩大单体的适用范围,可以使用链转移剂降低催化剂负载量,并且可以回收催化剂用于多次聚合。

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