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揭示具有低占据电荷分离态的聚嗪桥联 Ru(II)、Pt(II)超分子的亚单位变化,为作为 H2O 还原光催化剂产生 H2 的功能提供深入了解。

Subunit variation to uncover properties of polyazine-bridged Ru(II), Pt(II) supramolecules with low lying charge separated states providing insight into the functioning as H2O reduction photocatalysts to produce H2.

机构信息

Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24061-0212, United States.

出版信息

Inorg Chem. 2013 Sep 3;52(17):9749-60. doi: 10.1021/ic4004406. Epub 2013 Aug 13.

DOI:10.1021/ic4004406
PMID:23941111
Abstract

Two new structurally diverse polyazine-bridged Ru(II),Pt(II) tetrametallic complexes, {(Ph2phen)2Ru(dpp)}2Ru(dpp)PtCl26 (1a) and {(Ph2phen)2Ru(dpp)}2Ru(dpq)PtCl26 (2a) (Ph2phen = 4,7-diphenyl-1,10-phenanthroline, dpp = 2,3-bis(2-pyridyl)pyrazine, dpq = 2,3-bis(2-pyridyl)quinoxaline), as well as their trimetallic precursors have been synthesized to provide a comparison for detailed analysis to elucidate component effects in the previously reported photocatalyst {(phen)2Ru(dpp)}2Ru(dpq)PtCl26 (4a) (phen = 1,10-phenanthroline). Electrochemistry shows terminal Ru based highest occupied molecular orbitals (HOMOs) with remote BL' (BL' = bridging ligand coupling central Ru and cis-PtCl2 moiety) based lowest unoccupied molecular orbitals (LUMOs). Population of a lowest-lying charge separated ((3)CS) excited state with oxidized terminal Ru and reduced remote BL' via intramolecular electron transfer is predicted by electrochemical analysis and is observed through steady-state and time-resolved emission studies as well as emission excitation profiles which display unusual nonunity population of the lowest lying emissive Ru→dpp (3)MLCT (metal-to-ligand charge transfer) state. Each tetrametallic complex is an active photocatalyst for H2 production from H2O with 2a showing the highest activity (94 TON (turnover number) in 10 h, where TON = mol H2/mol catalyst). The nature of the bridging ligand coupling the trimetallic light absorber to the cis-PtCl2 moiety has a significant impact on the catalyst activity, correlated to the degree of population of the (3)CS excited state. The choice of terminal ligand affects visible light absorption and has a minor influence on photocatalytic H2 production from H2O. Evidence that an intact supramolecule functions as the photocatalyst includes a strong dependence of the photocatalysis on the identity of BL', an insensitivity to Hg(l), no detectable H2 production from the systems with the trimetallic synthons and cis-[PtCl2(DMSO)2] as well as spectroscopic analysis of the photocatalytic system.

摘要

两种新型结构多样的聚嗪桥联 Ru(II)、Pt(II)四金属配合物,{(Ph2phen)2Ru(dpp)}2Ru(dpp)PtCl26 (1a) 和 {(Ph2phen)2Ru(dpp)}2Ru(dpq)PtCl26 (2a)(Ph2phen = 4,7-二苯基-1,10-菲咯啉,dpp = 2,3-双(2-吡啶基)吡嗪,dpq = 2,3-双(2-吡啶基)喹喔啉),以及它们的三金属前体已经被合成,以提供一个比较详细的分析,阐明在以前报道的光催化剂{(phen)2Ru(dpp)}2Ru(dpq)PtCl26 (4a)(phen = 1,10-菲咯啉)中的成分效应。电化学显示终端 Ru 基最高占据分子轨道(HOMO)与远程 BL'(BL'=桥连配体耦合中心 Ru 和顺式-PtCl2 部分)基最低未占据分子轨道(LUMO)。通过电化学分析预测,通过分子内电子转移,从氧化的终端 Ru 到远程 BL'的最低电荷分离((3)CS)激发态的填充,以及通过稳态和时间分辨发射研究以及发射激发谱观察到这一点,这些研究显示出不寻常的非统一填充最低发光 Ru→dpp(3)MLCT(金属到配体电荷转移)态。每个四金属配合物都是 H2O 中 H2 产生的有效光催化剂,其中 2a 的活性最高(10 小时内 94 TON(周转数),其中 TON = mol H2/mol 催化剂)。桥连配体将三金属光吸收体与顺式-PtCl2 部分偶联的性质对催化剂活性有显著影响,与(3)CS 激发态的填充程度相关。终端配体的选择影响可见光吸收,对 H2O 中光催化 H2 产生的影响较小。作为光催化剂的超分子完整功能的证据包括光催化强烈依赖于 BL'的身份,对 Hg(l)不敏感,没有检测到三金属前体和顺式-[PtCl2(DMSO)2]系统以及光催化系统的光谱分析中的 H2 产生。

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