Smith Peter T, Benke Bahiru Punja, Cao Zhi, Kim Younghoon, Nichols Eva M, Kim Kimoon, Chang Christopher J
Department of Chemistry, University of California, Berkeley, Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720-1460, USA.
Center for Self-assembly and Complexity (CSC), Institute for Basic Science (IBS), Pohang, 37673, Republic of Korea.
Angew Chem Int Ed Engl. 2018 Jul 26;57(31):9684-9688. doi: 10.1002/anie.201803873. Epub 2018 Jul 5.
A porous organic cage composed of six iron tetraphenylporphyrins was used as a supramolecular catalyst for electrochemical CO -to-CO conversion. This strategy enhances active site exposure and substrate diffusion relative to the monomeric catalyst, resulting in CO generation with near-quantitative Faradaic efficiency in pH 7.3 water, with activities reaching 55 250 turnovers. These results provide a starting point for the design of supramolecular catalysts that can exploit the properties of the surrounding matrix yet retain the tunability of the original molecular unit.
一种由六个铁四苯基卟啉组成的多孔有机笼被用作电化学CO转化为CO的超分子催化剂。相对于单体催化剂,该策略增强了活性位点的暴露和底物扩散,从而在pH 7.3的水中以接近定量的法拉第效率产生CO,活性达到55250次周转。这些结果为超分子催化剂的设计提供了一个起点,该催化剂可以利用周围基质的性质,同时保留原始分子单元的可调性。