Structure and luminescent properties of 2D Salen-type lanthanide coordination polymers from the flexible N,N′-bis(salicylidene)-1,4-butanediamine ligand

被引:12
作者
Yue, Yumei [1 ]
Yan, Pengfei [1 ]
Sun, Jingwen [1 ]
Hou, Guangfeng [1 ]
Li, Guangming [1 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Minist Educ, Key Lab Funct Inorgan Mat Chem, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
Salen-type; Lanthanide coordination polymer; Luminescent property; Dinuclear; Methoxy bridged; METAL-ORGANIC FRAMEWORKS; SCHIFF-BASE COMPLEXES; TRIPLET-STATE ENERGY; HYDROTHERMAL SYNTHESIS; EXCITATION; CHEMISTRY; EU(III); DEVICES; FIELD;
D O I
10.1016/j.poly.2015.04.018
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new Salen-type lanthanide coordination polymers, [Ln(2)(H2L)(2)(NO3)(4)(CH3O)(2)] (Ln = Sm (1), Eu (2) and Lu (3); H2L = N,N'-bis(salicylidene)-1,4-butanediamine), have been synthesized by a solvothermal method and characterized by single-crystal X-ray diffraction, elemental analysis, IR spectra and thermo-gravimetric analysis. Single-crystal X-ray diffraction studies reveal that complexes 1-3 are isostructural 2D coordination polymers based on dinuclear units, where the mu(2)-(methoxy-O)(2)-bridged Ln(2)O(2) cores are linked by four Salen-type ligands in a bidentate mode. Each lanthanide ion is eight-coordinated by eight oxygen atoms, forming a distorted dodecahedral geometry. Luminescence analysis in the solid state at room temperature indicates that complex 1 exhibits the co-luminescence of the ligand and Sm-III ions and complex 2 shows the characteristic red luminescence of Eu-III ions. Furthermore, the energy transfer mechanisms are described and discussed. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 95
页数:6
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