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基于咪唑鎓和吡啶鎓的腙类化合物的可调聚集诱导发光及发射颜色

Tunable Aggregation-induced Emission and Emission Colors of Imidazolium and Pyridinium Based Hydrazones.

作者信息

Zhou Ying, Xie Puhui, Liu Lijie, Hao Changming, Qian Cheng, Guo Fengqi, Zheng Xin

机构信息

Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou, 450003, People's Republic of China.

College of Science, Henan Agricultural University, Zhengzhou, 450002, People's Republic of China.

出版信息

J Fluoresc. 2023 Nov;33(6):2201-2208. doi: 10.1007/s10895-023-03202-6. Epub 2023 Mar 31.

Abstract

Aggregation-induced emission (AIE) materials have drawn great attention for their wide applications as optical materials. The applications of AIE materials, however, are restricted by the complicated syntheses, hydrophobic properties and short emission wavelengths. Herein, an imidazolium based hydrazone (E)-1-(4-methoxyphenyl)-2-((1-methyl-1H-imidazol-2-yl)methylene)hydrazine hydrochloride (1) and a pyridinium based hydrazone (E)-1-(4-methoxyphenyl)-2-(pyridin-4-ylmethylene)hydrazine hydrochloride (2) have been synthesized. Notably, 1 and 2 in crystals show distinct green and near-infrared (NIR) fluorescence, with emission peaks at 530 and 688 nm, and Stokes shifts of 176 and 308 nm, respectively. After grinding the crystals to powder, the absolute fluorescence quantum yield (Φ) of 1 is increased from 4.2% to 10.6%, and the Φ of 2 is increased from 0.2% to 0.7%. X-ray crystallography studies together with theoretical calculations indicate that the enhanced emission of 1 arises from hydrogen bonding induced rigid network, and the fluorescence in the NIR region and large Stokes shift of 2 are attributed to its twisted molecular structure and strong push-pull effect.

摘要

聚集诱导发光(AIE)材料因其作为光学材料的广泛应用而备受关注。然而,AIE材料的应用受到复杂合成、疏水性质和短发射波长的限制。在此,合成了一种基于咪唑鎓的腙(E)-1-(4-甲氧基苯基)-2-((1-甲基-1H-咪唑-2-基)亚甲基)肼盐酸盐(1)和一种基于吡啶鎓的腙(E)-1-(4-甲氧基苯基)-2-(吡啶-4-基亚甲基)肼盐酸盐(2)。值得注意的是,晶体中的1和2呈现出明显的绿色和近红外(NIR)荧光,发射峰分别位于530和688 nm,斯托克斯位移分别为176和308 nm。将晶体研磨成粉末后,1的绝对荧光量子产率(Φ)从4.2%提高到10.6%,2的Φ从0.2%提高到0.7%。X射线晶体学研究和理论计算表明,1的发射增强源于氢键诱导的刚性网络,2在近红外区域的荧光和大斯托克斯位移归因于其扭曲的分子结构和强推拉效应。

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