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用于高效催化CO转化的咪唑盐功能化共价有机框架

Imidazolium-Salt-Functionalized Covalent Organic Frameworks for Highly Efficient Catalysis of CO Conversion.

作者信息

Qiu Jikuan, Zhao Yuling, Li Zhiyong, Wang Huiyong, Shi Yunlei, Wang Jianji

机构信息

Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Xinxiang, Henan, P. R. China.

College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu, 730000, P. R. China.

出版信息

ChemSusChem. 2019 Jun 7;12(11):2421-2427. doi: 10.1002/cssc.201900570. Epub 2019 May 2.

Abstract

The conversion of CO into valuable chemicals is an ideal pathway for CO utilization in industry, although the development of highly efficient catalysts remains a challenge. Herein, the design and synthesis of two covalent organic frameworks (COFs) functionalized with imidazolium salts were reported as catalysts for CO conversion. The resultant COFs possessed highly crystalline structures, showed high stability and surface area, and contained dense catalytic active sites on the pore walls. They exhibited outstanding catalytic performances for the reaction of CO with epoxides without any solvent or cocatalyst under mild conditions and afforded a record turnover number of 495 000. In addition, the COFs could serve as effective catalysts in the reductive reaction of CO with amines. The results presented here thus demonstrate the exceptional potential of the functionalized COFs for various challenging CO transformations.

摘要

将一氧化碳转化为有价值的化学品是工业上一氧化碳利用的理想途径,尽管开发高效催化剂仍然是一项挑战。在此,报道了两种用咪唑盐功能化的共价有机框架(COF)的设计与合成,作为一氧化碳转化的催化剂。所得的COF具有高度结晶的结构,表现出高稳定性和高比表面积,并且在孔壁上含有密集的催化活性位点。它们在温和条件下,无需任何溶剂或助催化剂,对一氧化碳与环氧化物的反应表现出出色的催化性能,周转数达到了创纪录的495000。此外,COF在一氧化碳与胺的还原反应中可作为有效的催化剂。因此,这里展示的结果证明了功能化COF在各种具有挑战性的一氧化碳转化反应中具有非凡的潜力。

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