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个人信息Personal Information
副教授
博士生导师
硕士生导师
性别:男
毕业院校:香港中文大学
学位:博士
所在单位:化工学院
学科:有机化学
办公地点:大连理工大学西校区,E-308
电子邮箱:liujh@dlut.edu.cn
Toward Controlling Water Oxidation Catalysis: Tunable Activity of Ruthenium Complexes with Axial Imidazole/DMSO Ligands
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论文类型:期刊论文
发表时间:2012-11-14
发表刊物:JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
收录刊物:SCIE、EI、Scopus
卷号:134
期号:45
页面范围:18868-18880
ISSN号:0002-7863
摘要:Using the combinations of imidazole and dimethyl :sulfoxide (DMSO) as axial ligands and 2,2'-bipyridine-6,6'-dicarboxylate (bda) as the equatorial ligand, we have synthesized six novel ruthenium complexes with noticeably different activity as water oxidation catalysts (WOCs). In four C-s symmetric Ru-II(kappa(3)-bda)(DMSO)L-2 complexes L = imidazole (1), N-methylimidazole (2), 5-methylimidazole (3), and 5-bromo-N-methylimidazole (4). Additionally, in two C-2v symmetric Ru-II(kappa(4)-bda)L-2 complexes L = 5-nitroimidazole (5) and 5-bromo-N-methylimidazole (6), that is, fully equivalent axial imidazoles. A detailed characterization of all complexes and the mechanistic investigation of the catalytic water oxidation have been carried out with a number of experimental techniques, that is, kinetics, electrochemistry and high resolution mass spectrometry (HR-MS), and density functional theory (DFT) calculations. We have observed the in situ formation: of a Ru-II-complex with the accessible seventh coordination position. The measured catalytic activities and kinetics of complex 1-6 revealed details about an important structure activity relation: the connection between the nature of axial ligands in the combination and either the increase or decrease of the catalytic activity. In particular, an axial DMSO group substantially increases the turnover frequency of WOCs reported in article, with the ruthenium-complex having one axial 5-bromo-N-methylimidazole and one axial DMSO: (4), we have obtained a high initial turnover frequency of similar to 180 s(-1). DFT modeling Of the binuclear reaction pathway of the O-O bond formation in catalytic Water oxidation further corroborated the concept of the mechanistic significance of the axial ligands and rationalized the experimentally observed difference in the activity of complexes with imidazole/DMSO and imidazole/imidazole combinations of axial ligands.