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作 者:Shao-Jun Hu Xiao-Qing Guo Li-Peng Zhou Li-Xuan Cai Qing-Fu Sun
机构地区:[1]State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou,Fujian 350002, China [2]College of Chemistry, Fuzhou University, Fuzhou, Fujian 350108, China,State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou,Fujian 350002, China [3]University of Chinese Academy of Sciences, Beijing 100049, China,State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou,Fujian 350002, China
出 处:《Chinese Journal of Chemistry》2019年第7期657-662,共6页中国化学(英文版)
基 金:the National Natural Science Foundation of China(.21825107,21601183,2017J05037);the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB20000000).
摘 要:Photo-functional supramolecular lanthanides assemblies have shown great potential in the materials and biomedical fields.Two new tri(tridentate) ligands (L3 and L4) highlighting small variation of the connection position to the central tridentate linkers have been designed,which leads to the emergent formation of either Ln3L3-type sandwich structures or Ln4L4-type tetrahedral cages.Moreover,nonlinear enhancement of lanthanide luminescence based on the modulation of inter-ligand charge-transfer states has been revealed on the mix-ligand Ln3L3 sandwiches.Our results provide important guidance for structure-design and photoluminescence optimization of supramolecular lanthanide-organic assemblies.
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