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极性噻唑衍生物在具有可逆光致变色性的混合氯酸铋中诱导的二次谐波响应。

Polar Thiazole Derivative-Induced Second Harmonic Response in Hybrid Bismuth Chlorate with Reversible Photochromism.

作者信息

Wang Ting-Jie, Guo Jin-Shuang, Zhang Ning-Ning, Li Yu, Li Cuncheng, Liu Guang-Ning

机构信息

Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, Shandong250022, P. R. China.

Characteristic Laboratory of Forensic Science in Universities of Shandong Province, Shandong University of Political Science and Law, Jinan, Shandong 250014, P. R. China.

出版信息

Inorg Chem. 2024 Oct 7;63(40):18955-18962. doi: 10.1021/acs.inorgchem.4c03315. Epub 2024 Sep 22.

Abstract

Inorganic-organic hybrid bismuth halides demonstrate great prospect in the field of second-order nonlinear optical (NLO) crystals because the ns electron on Bi(III) could lead to large molecular polarization and high second harmonic generation (SHG) coefficient on a noncentrosymmetric structure. However, researchers cannot yet control the effective arrangements of the bismuth halide functional motif, which results in SHG-active hybrid bismuth halides being rare. Herein, thiazole derivatives with a polar donor-π-acceptor system are designed to explore hybrid bismuth halide NLO crystals. The protonated 2-(4-hydroxyphenyl) thiazole (denoted as hpt) interacts with the (BiCl) motif via H···Cl hydrogen bonds to prevent antiparallel arrangements, which therefore enhance the NLO property. crystallizes in the monoclinic polar 2 space group, which exhibits a strong SHG response and reversible photochromic behavior. Structural analysis and theory calculations reveal that the synergistic effect between the polar thiazole derivative and the distorted inorganic [BiCl] motif is responsible for the SHG response. This is the first report of polar thiazole derivative-induced SHG-active hybrid bismuth halide coupled with reversible photochromism.

摘要

无机-有机杂化卤化铋在二阶非线性光学(NLO)晶体领域展现出巨大前景,因为Bi(III)上的ns电子可在非中心对称结构上导致较大的分子极化和高二阶谐波产生(SHG)系数。然而,研究人员尚未能控制卤化铋功能基序的有效排列,这导致具有SHG活性的杂化卤化铋十分罕见。在此,设计了具有极性供体-π-受体体系的噻唑衍生物,以探索杂化卤化铋NLO晶体。质子化的2-(4-羟基苯基)噻唑(记为hpt)通过H···Cl氢键与(BiCl)基序相互作用,防止反平行排列,从而增强NLO性能。其晶体属于单斜极性2空间群,表现出强烈的SHG响应和可逆光致变色行为。结构分析和理论计算表明,极性噻唑衍生物与畸变的无机[BiCl]基序之间的协同效应是SHG响应的原因。这是关于极性噻唑衍生物诱导的具有SHG活性的杂化卤化铋并伴有可逆光致变色的首次报道。

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