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异多核超分子铽/镱组装体在水中的分子上转换

Molecular Upconversion in Water in Heteropolynuclear Supramolecular Tb/Yb Assemblies.

作者信息

Nonat Aline, Bahamyirou Sylvana, Lecointre Alexandre, Przybilla Frédéric, Mély Yves, Platas-Iglesias Carlos, Camerel Franck, Jeannin Olivier, Charbonnière Loïc J

机构信息

Equipe de Synthèse pour l'Analyse (SynPA), Institut Pluridisciplinaire Hubert Curien (IPHC, UMR 7178) , CNRS/Université de Strasbourg , ECPM, 25 Rue Becquerel , 67087 Strasbourg Cedex, France.

Laboratoire de Bioimagerie et Pathologies, CNRS UMR 7021, Faculté de Pharmacie CS60024 74, Route du Rhin , 67401 Illkirch-Graffenstaden , France.

出版信息

J Am Chem Soc. 2019 Jan 30;141(4):1568-1576. doi: 10.1021/jacs.8b10932. Epub 2019 Jan 16.

Abstract

Piling up excited states to reach upconversion (UC) is severely restricted by vibrational quenching mechanisms, especially when one looks at discrete molecular entities in solution. By carefully controlling the supramolecular assembly processes resulting from the strong electrostatic interactions between negatively charged Yb complexes and Tb cations in aqueous solutions, we engineered the formation of heteropolynuclear complexes of [(YbL)Tb ] compositions ( x = 1 and 2). These edifices display a phenomenon of cooperative photosensitization UC with green emission of the Tb cations upon NIR excitation at 980 nm in the Yb absorption band. The photophysical properties of the complexes were carefully investigated by steady-state and time-resolved luminescence experiments in DO, allowing one to quantify the impact of the composition and pD of the solution on the emission intensity as well as clarifying the exact cooperative photosensitization upconversion mechanism. Using optimized conditions, the energy transfer UC process could be observed for the first time in nondeuterated water with discrete molecular compounds.

摘要

通过振动猝灭机制,堆积激发态以实现上转换(UC)受到严重限制,尤其是当观察溶液中的离散分子实体时。通过仔细控制水溶液中带负电荷的Yb配合物与Tb阳离子之间强静电相互作用产生的超分子组装过程,我们设计合成了[(YbL)Tb ]组成(x = 1和2)的异多核配合物。这些结构在980 nm近红外光激发下,于Yb吸收带中呈现Tb阳离子的绿色发射协同光敏上转换现象。通过在重水中进行稳态和时间分辨发光实验,对配合物的光物理性质进行了仔细研究,从而能够量化溶液组成和pD对发射强度的影响,并阐明确切的协同光敏上转换机制。在优化条件下,首次在非重水的离散分子化合物中观察到了能量转移上转换过程。

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