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添加融合给体-受体配体对 Ru(II) 配合物的影响:[Ru(TTF-dppz)2(Aqphen)]2+的合成、表征和光诱导电子转移反应。

Effect of the addition of a fused donor-acceptor ligand on a Ru(II) complex: synthesis, characterization, and photoinduced electron transfer reactions of [Ru(TTF-dppz)2(Aqphen)]2+.

机构信息

Département de Chimie Physique, Université de Genève, 30 Quai Ernest-Ansermet, CH-1211 Genève 4, Switzerland.

出版信息

Inorg Chem. 2011 Apr 18;50(8):3295-303. doi: 10.1021/ic101951n. Epub 2011 Mar 17.

Abstract

The synthesis and the photophysical properties of the complex Ru(TTF-dppz)(2)(Aqphen) (TTF = tetrathiafulvalene, dppz = dipyrido-[3,2-a:2',3'-c]phenazine, Aqphen = anthraquinone fused to phenanthroline via a pyrazine bridge) are described. In this molecular triad excitation into the metal-ligand charge transfer bands results in the creation of a long-lived charge separated state with TTF acting as electron donor and anthraquinone as terminal acceptor. The lifetime of the charge-separated state is 400 ns in dichloromethane at room temperature. A mechanism for the charge separation involving an intermediate charge-separated state is proposed based on transient absorption spectroscopy.

摘要

描述了配合物Ru(TTF-dppz)(2)(Aqphen)(TTF=四硫富瓦烯,dppz=二吡啶并[3,2-a:2',3'-c]吩嗪,Aqphen=通过吡嗪桥连接到菲咯啉的蒽醌)的合成和光物理性质。在这个分子三联体中,激发到金属-配体电荷转移带导致形成长寿命的电荷分离态,其中 TTF 作为电子供体,蒽醌作为末端受体。在室温下的二氯甲烷中,电荷分离态的寿命为 400 纳秒。基于瞬态吸收光谱,提出了一种涉及中间电荷分离态的电荷分离机制。

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