Selective formation of luminescent chiral cocrystal:Molecular self-assembly of 2,20-binaphthol and 2-(3-pyridyl)-1H-benzimidazole
Selective formation of luminescent chiral cocrystal:Molecular self-assembly of 2,20-binaphthol and 2-(3-pyridyl)-1H-benzimidazole作者机构:State Key Laboratory of Chemical Resource EngineeringBeijing University of Chemical Technology Key Laboratory of Theoretical and Computational PhotochemistryMinistry of EducationCollege of ChemistryBeijing Normal University
出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))
年 卷 期:2018年第29卷第10期
页 面:1541-1543页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学]
基 金:supported by the National Natural Science Foundation of China(NSFC, Nos. 21771021 and 21473013) the National Basic Research Program of China(973 Program, No. 2014CB932103) Beijing Municipal Natural Science Foundation (No. 2152016)
主 题:Chiral cocrystal Molecular self-assembly Binaphthol
摘 要:Luminescent cocrystals have been received much attention in fluorescence imaging and sensor application. In this work, we report that the high-quality chiral luminescent cocrystal can be obtained through a molecular self-assembly process of 2,20-binaphthol and 2-(3-pyridyl)-1 H-benzimidazole. The assembly modes and stacking fashions of as-obtained cocrystal were determined by single crystal X-ray diffractometer. The structure and optical properties of the cocrystals were characterized by fluorescence emission, fluorescence decay, Raman and circular dichroism spectra. The results show that both the pristine co-assembled units(R-BINOL and S-BINOL) give rise to the R conformation within the final cocrystal, suggesting that the formation of cocrystal can be an effective way to achieve R/S-isomeric transformation of 2,20-binaphthol. It is also expected that the co-crystallization approach has much flexibility and potential applications for the design and selective formation of chiral luminescent materials.