电催化剂
卟啉
催化作用
锑
化学
氧化还原
配体(生物化学)
质子
光化学
组合化学
无机化学
电化学
物理化学
有机化学
电极
受体
量子力学
物理
生物化学
作者
Jianbing Jiang,Kelly L. Materna,Svante Hedström,Ke Yang,Robert H. Crabtree,Víctor S. Batista,Gary W. Brudvig
标识
DOI:10.1002/anie.201704700
摘要
Abstract Main‐group complexes are shown to be viable electrocatalysts for the H 2 ‐evolution reaction (HER) from acid. A series of antimony porphyrins with varying axial ligands were synthesized for electrocatalysis applications. The proton‐reduction catalytic properties of TPSb(OH) 2 (TP=5,10,15,20‐tetra( p ‐tolyl)porphyrin) with two axial hydroxy ligands were studied in detail, demonstrating catalytic H 2 production. Experiments, in conjunction with quantum chemistry calculations, show that the catalytic cycle is driven via the redox activity of both the porphyrin ligand and the Sb center. This study brings insight into main group catalysis and the role of redox‐active ligands during catalysis.
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