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单核钌(II)单水配合物的化学计量光异构化控制氧化还原性质和水氧化催化。

Stoichiometric photoisomerization of mononuclear ruthenium(II) monoaquo complexes controlling redox properties and water oxidation catalysis.

机构信息

Department of Materials Science and Technology, Faculty of Engineering, and Center for Transdisciplinary Research, Niigata University, 8050 Ikarashi-2, Niigata 950-2181, Japan.

出版信息

J Am Chem Soc. 2011 Jun 15;133(23):8846-9. doi: 10.1021/ja2024228. Epub 2011 May 24.

Abstract

Although various reactions involved in photoexcited states of polypyridyl ruthenium(II) complexes have been extensively studied, photoisomerization of the complexes is very rare. We report the first illustration of stoichiometric photoisomerization of trans-Ru(tpy)(pynp)OH(2) (1a) [tpy = 2,2':6',2''-terpyridine; pynp = 2-(2-pyridyl)-1,8-naphthyridine] to cis-Ru(tpy)(pynp)OH(2) (1a') and the isolation of 1a and 1a' for X-ray crystallographic analysis. Polypyridyl ruthenium(II) aquo complexes are attracting much attention related to proton-coupled electron transfer and water oxidation catalysis. We demonstrate that the photoisomerization significantly controls the redox reactions and water oxidation catalyses involving the ruthenium(II) aquo complexes 1a and 1a'.

摘要

尽管已经广泛研究了多吡啶钌(II)配合物的光激发态中涉及的各种反应,但该配合物的光异构化非常罕见。我们首次报道了反式-Ru(tpy)(pynp)OH(2)(1a)[tpy=2,2':6',2''-三联吡啶;pynp=2-(2-吡啶基)-1,8-萘啶]与顺式-Ru(tpy)(pynp)OH(2)(1a')的化学计量比光异构化,并分离出 1a 和 1a'进行 X 射线晶体学分析。多吡啶钌(II)水合配合物由于与质子耦合电子转移和水氧化催化有关而受到广泛关注。我们证明,光异构化显著控制了涉及钌(II)水合配合物 1a 和 1a'的氧化还原反应和水氧化催化。

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