钴
化学
催化作用
电子顺磁共振
氧化态
氧化剂
过电位
氧化还原
配体(生物化学)
光化学
金属
催化氧化
无机化学
组合化学
有机化学
物理化学
电化学
核磁共振
生物化学
物理
受体
电极
作者
Yun‐Fei Su,Wenzhi Luo,Wang‐qiang Lin,Yibing Su,Zi‐Jian Li,Yongjun Yuan,Jianfeng Li,Guang‐Hui Chen,Zhaosheng Li,Zhen‐Tao Yu,Zhigang Zou
标识
DOI:10.1002/anie.202201430
摘要
Abstract Herein, we present a stable water‐soluble cobalt complex supported by a dianionic 2,2′‐([2,2′‐bipyridine]‐6,6′‐diyl)bis(propan‐2‐ol) ligand scaffold, which is a rare example of a high‐oxidation species, as demonstrated by structural, spectroscopic and theoretical data. Electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements revealed that the Co IV center of the mononuclear complex in the solid state resides in the high spin state (sextet, S =5/2). The complex can effectively catalyze water oxidation via a single‐site water nucleophilic attack pathway with an overpotential of only 360 mV in a phosphate buffer with a pH of 6. The key intermediate toward water oxidation was speculated based on theoretical calculations and was identified by in situ spectroelectrochemical experiments. The results are important regarding the accessibility of high‐oxidation state metal species in synthetic models for achieving robust and reactive oxidation catalysis.
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