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受生物启发的四核锰配合物中类光系统II的水氧化机制

Photosystem II like water oxidation mechanism in a bioinspired tetranuclear manganese complex.

作者信息

Liao Rong-Zhen, Kärkäs Markus D, Lee Bao-Lin, Åkermark Björn, Siegbahn Per E M

机构信息

Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University , SE-10691 Stockholm, Sweden.

出版信息

Inorg Chem. 2015 Jan 5;54(1):342-51. doi: 10.1021/ic5024983. Epub 2014 Dec 8.

Abstract

The synthesis of Mn-based catalysts to mimic the structural and catalytic properties of the oxygen-evolving complex in photosystem II is a long-standing goal for researchers. An interesting result in this field came with the synthesis of a Mn complex that enables water oxidation driven by the mild single-electron oxidant Ru(bpy)3. On the basis of hybrid density functional calculations, we herein propose a water oxidation mechanism for this bioinspired Mn catalyst, where the crucial O-O bond formation proceeds from the formal Mn4(IV,IV,IV,V) state by direct coupling of a Mn(IV)-bound terminal oxyl radical and a di-Mn bridging oxo group, a mechanism quite similar to the presently leading suggestion for the natural system. Of importance here is that the designed ligand is shown to be redox-active and can therefore store redox equivalents during the catalytic transitions, thereby alleviating the redox processes at the Mn centers.

摘要

合成锰基催化剂以模拟光系统II中析氧复合物的结构和催化性能,一直是研究人员长期以来的目标。该领域一项有趣的成果是合成了一种锰配合物,它能使由温和的单电子氧化剂[Ru(bpy)₃]³⁺驱动的水氧化反应发生。基于杂化密度泛函计算,我们在此提出了这种受生物启发的锰催化剂的水氧化机制,其中关键的O - O键形成是通过与锰(IV)相连的末端氧自由基和双锰桥连氧基团直接偶联,从形式上的Mn₄(IV,IV,IV,V)状态开始的,这一机制与目前对自然系统的主要推测非常相似。这里重要的是,所设计的配体被证明具有氧化还原活性,因此可以在催化转变过程中储存氧化还原当量,从而减轻锰中心的氧化还原过程。

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