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有机分子的刚性化或相互作用诱导磷光

Rigidification or interaction-induced phosphorescence of organic molecules.

作者信息

Baroncini Massimo, Bergamini Giacomo, Ceroni Paola

机构信息

Department of Chemistry "Giacomo Ciamician" and Interuniversity Center for the Chemical Conversion of Solar Energy (SolarChem), University of Bologna, Via Selmi 2, 40126 Bologna, Italy.

出版信息

Chem Commun (Camb). 2017 Feb 9;53(13):2081-2093. doi: 10.1039/c6cc09288h.

Abstract

Phosphorescent materials are mostly based on metal complexes. Metal-free organic molecules usually display phosphorescence only in a rigid matrix at 77 K. In the last few years, there has been increasing interest in the design of organic molecules displaying long-lived and highly intense room-temperature phosphorescence, an extremely difficult task since these two properties are generally conflicting. This review reports the most recent and tutorial examples of molecules that are weakly or non-phosphorescent in deaerated fluid solution and whose room temperature phosphorescence is switched on upon aggregation. The examples are divided into two classes according to the mechanism responsible for switching on phosphorescence: (i) rigidification by crystallization or by encapsulation in a polymeric matrix and (ii) interaction with other molecules of the same type (self-aggregation) or a different type by taking advantage of heavy-atom effects.

摘要

磷光材料大多基于金属配合物。无金属有机分子通常仅在77 K的刚性基质中显示磷光。在过去几年中,人们对设计具有长寿命和高强度室温磷光的有机分子越来越感兴趣,这是一项极其困难的任务,因为这两种性质通常相互矛盾。本综述报道了在脱气流体溶液中弱磷光或无磷光且在聚集时开启室温磷光的分子的最新示例及教程示例。这些示例根据开启磷光的机制分为两类:(i) 通过结晶或封装在聚合物基质中实现刚性化,以及(ii) 通过利用重原子效应与相同类型(自聚集)或不同类型的其他分子相互作用。

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