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用于聚集诱导发光的激发驱动高价锡(IV)化合物的制备及其在冰点以下热响应发光薄膜中的应用。

Creation of Excitation-Driven Hypervalent Tin(IV) Compounds For Aggregation-Induced Emission and Application to Thermoresponsive Luminescent Films Below Freezing Point.

作者信息

Gon Masayuki, Shibahara Keisuke, Tanimura Kazuya, Tanaka Kazuo

机构信息

Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Katsura, Kyoto, 615-8510, Japan.

Department of Technology and Ecology, Graduate School of Global Environmental Studies, Kyoto University, Katsura, Nishikyo-ku, Kyoto, 615-8510, Japan.

出版信息

Chem Asian J. 2024 Dec 16;19(24):e202401094. doi: 10.1002/asia.202401094. Epub 2024 Oct 31.

Abstract

Although many researchers have devoted their much effort to establish the strategy for developing a stimuli-responsive molecule and tuning of their properties according to the preprogrammed design, it is still challenging to create desired molecules from the scratch. We recently demonstrated that the molecules with a large structural difference between the theoretically optimized structures in the ground and excited states have a potential to exhibit stimuli-responsive luminescent properties. We defined these molecules as an excitation-driven molecule and have shown that they are a versatile platform for designing stimuli-responsive luminescent molecules. Herein, based on the concept of excitation-driven molecules, we show that the hypervalent tin-fused azomethine (TAm) compounds possessing aggregation-induced emission (AIE) properties can be obtained by simple chemical modification with a methyl group although conventional TAm derivatives are well known to be highly luminescent compounds in solution. Furthermore, by combining the solid-state luminescence property of AIE and the coordination number shifts of the hypervalent tin atom, the thermoresponsive films operating below the freezing point are fabricated with the polymer. In this study, we apply the concept of excitation-driven molecules to the hypervalent compounds and demonstrate to obtain the novel functional materials.

摘要

尽管许多研究人员付出了巨大努力来建立开发刺激响应分子的策略,并根据预先设定的设计调整其性质,但从头开始创建所需分子仍然具有挑战性。我们最近证明,在基态和激发态下理论优化结构之间存在巨大结构差异的分子具有展现刺激响应发光性质的潜力。我们将这些分子定义为激发驱动分子,并表明它们是设计刺激响应发光分子的通用平台。在此,基于激发驱动分子的概念,我们表明,尽管传统的高价锡-甲亚胺(TAm)衍生物在溶液中是众所周知的高发光化合物,但通过用甲基进行简单的化学修饰,可以获得具有聚集诱导发光(AIE)性质的高价锡稠合甲亚胺(TAm)化合物。此外,通过结合AIE的固态发光性质和高价锡原子的配位数变化,用该聚合物制备了在冰点以下工作的热响应薄膜。在本研究中,我们将激发驱动分子的概念应用于高价化合物,并证明可以获得新型功能材料。

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