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通过多重堆积相互作用诱导的金属俄罗斯套娃和金属[2]连环烷的自组装及光热转换

Self-Assembly and Photothermal Conversion of MetallaRussian Doll and Metalla[2]catenanes Induced via Multiple Stacking Interactions.

作者信息

Chen Tian, Zhao Ying, Dang Li-Long, Zhang Ting-Ting, Lu Xiao-Li, Chai Yin-Hang, Lu Ming-Yu, Aznarez Francisco, Ma Lu-Fang

机构信息

College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471934, P. R. China.

College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China.

出版信息

J Am Chem Soc. 2023 Aug 16;145(32):18036-18047. doi: 10.1021/jacs.3c05720. Epub 2023 Jul 17.

Abstract

A variety of organometallic supramolecular architectures have been constructed over the past decades and their properties were also explored via different strategies. However, the synthesis of metalla-Russian doll is still a fascinating challenge. Herein, a series of new coordination supramolecular complexes, including a metalla-Russian doll, metalla[2]catenanes, and metallarectangles, were synthesized by using meticulously selected CpRh (Cp = η-CMe) building units (E1, E2, and E3) and three rigid anthracylpyridine ligands (L1, L2, and L3) via a self-assembly strategy. While the combination of the short ligand L1 and E1 or E2 generated two metallarectangles, the longer ligand L2 containing an alkynyl group resulted in two new [2]catenanes, most likely due to which the strong electron-donating effect of alkynyl groups causes self-accumulation. Interestingly, an unusual Russian doll assembly was obtained through the reaction of L3 and E3 based on sextuple π···π stacking interactions. Furthermore, the dynamic structural conversion between [2]catenanes and the corresponding metallarectangles could be observed through concentration-, solvent-, and guest-induced effects. The [2]catenane complexes 4b displayed efficient photothermal conversion efficiency in solution (20.2%), in comparison with other organometallic macrocycles. We believe that π···π stacking interactions generate active nonradiative pathways and promote radiative photodeactivation pathways. This study proves the versatility of half-sandwich building units, not only to build complicated supramolecular topologies but also in effective functional materials for various appealing applications.

摘要

在过去几十年中,人们构建了各种各样的有机金属超分子结构,并通过不同策略探索了它们的性质。然而,金属俄罗斯套娃的合成仍然是一个极具吸引力的挑战。在此,通过自组装策略,使用精心挑选的CpRh(Cp = η-CMe)构建单元(E1、E2和E3)和三种刚性蒽基吡啶配体(L1、L2和L3)合成了一系列新的配位超分子配合物,包括金属俄罗斯套娃、金属[2]连环烷和金属矩形。短配体L1与E1或E2的组合生成了两个金属矩形,而含有炔基的较长配体L2则产生了两个新的[2]连环烷,这很可能是由于炔基的强给电子效应导致了自堆积。有趣的是,基于六重π···π堆积相互作用,通过L3和E3的反应获得了一种不寻常的俄罗斯套娃组装体。此外,通过浓度、溶剂和客体诱导效应,可以观察到[2]连环烷与相应金属矩形之间的动态结构转换。与其他有机金属大环化合物相比,[2]连环烷配合物4b在溶液中表现出高效的光热转换效率(20.2%)。我们认为,π···π堆积相互作用产生了活跃的非辐射途径,并促进了辐射光失活途径。这项研究证明了半夹心构建单元的多功能性,不仅可以构建复杂的超分子拓扑结构,还可以用于各种有吸引力应用的有效功能材料。

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