Fu Hong-Ru, Zhang Ruo-Yu, Li Ting, Wei Chen-Ying, Liu Shuang, Xu Jia-Yi, Zhu Xueli, Wei Jiaojiao, Ding Qing-Rong, Ma Lu-Fang
College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471934, China.
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China.
Chem Commun (Camb). 2024 Sep 12;60(74):10212-10215. doi: 10.1039/d4cc03164d.
Herein, chiral metal-organic frameworks (MOFs), DCF-20 and LCF-20, were utilized as matrices for both chirality transfer and energy transfer. HBT1@MOFs and HBT2@MOFs emit excitation-dependent circularly polarized luminescence (CPL) due to excited-state intramolecular proton transfer (ESIPT). HBT1/C152/NIR@MOFs exhibit full-color and white CPL. The luminescence dissymmetry factors () were significantly increased, benefiting from the efficient chirality space transfer and high luminescence efficiency.
在此，手性金属有机框架（MOF）DCF - 20和LCF - 20被用作手性转移和能量转移的基质。由于激发态分子内质子转移（ESIPT），HBT1@MOF和HBT2@MOF发出依赖于激发的圆偏振发光（CPL）。HBT1/C152/NIR@MOF表现出全色和白色CPL。得益于高效的手性空间转移和高发光效率，发光不对称因子（）显著增加。
