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基于咪唑的激发态分子内质子转移材料:大单晶的合成与放大自发辐射

Imidazole-based excited-state intramolecular proton-transfer materials: synthesis and amplified spontaneous emission from a large single crystal.

作者信息

Park Sanghyuk, Kwon Oh-Hoon, Kim Sehoon, Park Sangwoo, Choi Moon-Gun, Cha Myoungsik, Park Soo Young, Jang Du-Jeon

机构信息

School of Materials Science and Engineering, Seoul National University, ENG 445, Seoul 151-744, Korea.

出版信息

J Am Chem Soc. 2005 Jul 20;127(28):10070-4. doi: 10.1021/ja0508727.

Abstract

We have synthesized a novel class of imidazole-based excited-state intramolecular proton-transfer (ESIPT) materials, i.e., hydroxy-substituted tetraphenylimidazole (HPI) and its derivative HPI-Ac, which formed large single crystals exhibiting intense blue fluorescence and amplified spontaneous emission (ASE). Transparent, clear, and well-defined fluorescent single crystals of HPI-Ac as large as 20 mm x 25 mm x 5 mm were easily grown from its dilute solution. From the X-ray crystallographic analysis and semiempirical molecular orbital calculation, it was deduced that the four phenyl groups substituted into the imidazole ring of HPI and HPI-Ac allowed the crystals free from concentration quenching of fluorescence by limiting the excessive tight-stacking responsible for intermolecular vibrational coupling and relevant nonradiative relaxation. Fluorescence spectral narrowing and efficient ASE were observed in the HPI-Ac single crystal even at low excitation levels attributed to the intrinsic four-level ESIPT photocycle.

摘要

我们合成了一类新型的基于咪唑的激发态分子内质子转移(ESIPT)材料,即羟基取代的四苯基咪唑(HPI)及其衍生物HPI-Ac,它们形成了呈现强烈蓝色荧光和放大自发辐射(ASE)的大单晶。从其稀溶液中很容易生长出尺寸达20 mm×25 mm×5 mm的透明、清澈且轮廓清晰的HPI-Ac荧光单晶。通过X射线晶体学分析和半经验分子轨道计算推断,取代到HPI和HPI-Ac咪唑环上的四个苯基通过限制导致分子间振动耦合和相关非辐射弛豫的过度紧密堆积,使晶体免受荧光浓度猝灭。即使在低激发水平下,由于固有的四能级ESIPT光循环,在HPI-Ac单晶中也观察到了荧光光谱变窄和高效的ASE。

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