| Literature DB >> 31967403 |
Xuan Gong1, Yufei Shu1, Zhuo Jiang1, Lingxiang Lu2, Xiaohui Xu3, Chao Wang1, Hexiang Deng1,4.
Abstract
Discoveries of the accurate spatial arrangement of active sites in biological systems and cooperation between them for high catalytic efficiency are two major events in biology. However, precise tuning of these aspects is largely missing in the design of artificial catalysts. Here, a series of metal-organic frameworks (MOFs) were used, not only to overcome the limit of distance between active sites in bio-systems, but also to unveil the critical role of this distance for efficient catalysis. A linear correlation was established between photocatalytic activity and the reciprocal of inter active-site distance; a smaller distance led to higher activity. Vacancies created at selected crystallographic positions of MOFs promoted their photocatalytic efficiency. MOF-525-J33 with 15.6 Å inter active-site distance and 33 % vacancies exhibited unprecedented high turnover frequency of 29.5 h-1 in visible-light-driven acceptorless dehydrogenation of tetrahydroquinoline at room temperature.Entities:
Keywords: active-site distance; dehydrogenation; metal-organic frameworks; photocatalysis; porphyrins
Year: 2020 PMID: 31967403 DOI: 10.1002/anie.201915537
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336