Lanthanide coordination polymers assembled from triazine-based flexible polycarboxylate ligands and their luminescent properties

被引:23
|
作者
Huang, Yihui [1 ,2 ]
Zhu, Qilong [1 ,2 ]
Sheng, Tianlu [1 ]
Hu, Shengmin [1 ]
Fu, Ruibiao [1 ]
Shen, Chaojun [1 ]
Tan, Chunhong [1 ,2 ]
Wen, Yuehong [1 ]
Bai, Songyan [1 ,2 ]
Wu, Xintao [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
基金
美国国家科学基金会;
关键词
INTRAMOLECULAR ENERGY-TRANSFER; METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; HIGHLY LUMINESCENT; MAGNETIC-PROPERTIES; SUPRAMOLECULAR CHEMISTRY; COMPLEXES; PHOTOLUMINESCENCE; SERIES; ACID;
D O I
10.1039/c3ce27020c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two flexible triazine-based polycarboxylate ligands, 1,3,5-triazine-2-iminodiacetic acid-4,6-bis(L-alanine) (H(4)L1) and 1,3,5-triazine-2-iminodiacetic acid-4,6-biglycine (H4L2), have been designed and used to construct a series of luminescent lanthanide coordination polymers {[Ln(HL1)](H2O)(5)}(n) (Ln = 1, Tb; 2, Eu; 3, Gd) and {[Ln(HL2)(H2O)](H2O)(2)}(n) (Ln = 4, Tb; 5, Eu; 6, Gd). The complexes were structurally authenticated by single-crystal X-ray diffraction, revealing that isostructural complexes 1-3, derived from H(4)L1, possess a 2-D framework with the monoclinic space group C2/c, whereas isostructural complexes 4-6, based on H(4)L2, exhibit a 2-D layer structure with the monoclinic space group P2(1)/c. Solid-state photoluminescence properties of the complexes were investigated. Complexes 1 and 2 exhibit remarkable green and red luminescence emissions with high quantum yields up to 67% and 68%, respectively, and millisecond-level lifetimes. Nevertheless, complexes 4 and 5 feature weak quantum yields (9.9% for 4; and 30% for 5).
引用
收藏
页码:3560 / 3567
页数:8
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