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多核钌(II)多吡啶配合物中的汇聚能量转移:发光性质的显著增强

Converging Energy Transfer in Polynuclear Ru(II) Multiterpyridine Complexes: Significant Enhancement of Luminescent Properties.

作者信息

Cerfontaine Simon, Marcélis Lionel, Laramee-Milette Baptiste, Hanan Garry S, Loiseau Frédérique, De Winter Julien, Gerbaux Pascal, Elias Benjamin

机构信息

Institut de la Matière Condensée et des Nanosciences (IMCN) - Molécules, Solides et Réactivité (MOST) , Université catholique de Louvain , Place Louis Pasteur 1, bte L4.01.02 , B-1348 Louvain-la-Neuve , Belgium.

Département de Chimie , Université de Montréal 2900 Edouard-Montpetit , Montréal , Québec H3T-1J4 , Canada.

出版信息

Inorg Chem. 2018 Mar 5;57(5):2639-2653. doi: 10.1021/acs.inorgchem.7b03040. Epub 2018 Feb 21.

Abstract

Ruthenium-based complexes are widely used as photocatalysts, as photosensitizers, or as building blocks for supramolecular assemblies. In the field of solar energy conversion, building light harvesting antenna is of prime interest. Nevertheless, collecting light is mandatory but not sufficient; once collected and transferred, the exciton has to be long-lived enough to be transferred to a catalytic site. If Ru(II) terpyridine complexes are prime building blocks for structural reasons, the short lifetime of their excited state prevents their use as a harvesting center in light antennae. In this paper, we present new polynuclear assemblies, based on Ru(II)-terpyridine units where delocalization of the excited state is combined with an antenna effect. As a consequence, complexes C1-C3 display long-lived excited states compared to [Ru(tpy)], making them promising efficient antenna building blocks to be connected to a final acceptor or a catalytic center.

摘要

钌基配合物被广泛用作光催化剂、光敏剂或超分子组装体的构建单元。在太阳能转换领域,构建光捕获天线备受关注。然而,收集光虽是必要的,但并不充分;激子一旦被收集并转移,必须具有足够长的寿命才能转移到催化位点。如果说钌(II)三联吡啶配合物因结构原因是主要的构建单元,那么其激发态的短寿命使其无法用作光天线中的捕获中心。在本文中,我们展示了基于钌(II)-三联吡啶单元的新型多核组装体,其中激发态的离域与天线效应相结合。因此,与[Ru(tpy)]相比,配合物C1 - C3显示出长寿命的激发态,使其有望成为连接到最终受体或催化中心的高效天线构建单元。

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