期刊
CHEMNANOMAT
卷 5, 期 12, 页码 1467-1470出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cnma.201900432
关键词
metal-organic frameworks; photocatalysis; hydrogen; organometallic complex; visible-light
资金
- JST ACCEL, Japan [JPMJAC1302]
- Ministry of Education, culture, Sports, Science and Technology of Japan [15K17903, 15K13820, 18K14305]
- Global Research Program of the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology (MEST), Korea [2010-00339]
- Heiwa Nakajima Foundation
- Grants-in-Aid for Scientific Research [15K13820, 18K14305, 15K17903] Funding Source: KAKEN
Integration of photocatalytic polypyridyl complexes inside metal-organic frameworks (MOFs) backbone has been so far mostly achieved by utilization of bipyridine dicarboxylic acid as a linker. This fact limits the possibility of hosts that can be used amongst the countless MOFs existing. In this study, by using UiO-66-NH2 as a stable platform, postsynthetic modification (PSM) of the amino groups in organic linkers with 2-pyridinecarboxaldehyde and K2PtCl4 was applied to create a N,N-chelating ligand and simultaneous coordination of Pt2+ ions in a one-pot approach. XAFS and H-1 NMR analyses confirmed the creation of pyridylimine Pt(II) complexes. The composites showed viable activity towards photocatalytic hydrogen evolution reaction under visible light irradiation. Recyclability and leaching tests demonstrated their high stability and function as heterogeneous catalysts.
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