Synthesis and Characterization of New Coordination Polymers with Tunable Luminescent Properties Generated from Bent 1,2,4-Triazole-Bridged N,N′-Dioxides and Ln(III) Salts

被引:33
作者
Wang, Hai-Ying [1 ]
Cheng, Jun-Yan [1 ]
Ma, Jian-Ping [1 ]
Dong, Yu-Bin [1 ]
Huang, Ru-Qi [1 ]
机构
[1] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Mol & Nano Probe,Minist Educ, Engn Res Ctr Pesticide & Med Intermediate Clean P, Jinan 250014, Peoples R China
基金
中国国家自然科学基金;
关键词
CHIRAL LANTHANIDE COMPLEXES; ORGANIC ROTAXANE FRAMEWORKS; LIGANDS; AG(I); ADSORPTION; DINUCLEAR; EUROPIUM; DISCRETE; NETWORKS; ANION;
D O I
10.1021/ic902311g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new bent 1, 2,4-triazole-bridged N,N'-dioxide ligand, namely, 3,5-bis(3-pyridyl-N-oxide)-4-amino-1,2,4-triazole (L2), was designed and synthesized by the oxidation of 3,5-bis(3-pyridyl)-4-amino-1,2,4-triazole with H2O2 in the presence of HOAc at ambient temperatures. Eleven Ln(III)-based coordination polymers have been successfully prepared by the solution reactions of L2 with various Ln(III) -perchlorates. The structures of these new Ln(III) polymers clearly reflect the effect of the lanthanide contraction. Compounds 1-6 feature a two-dimensional net, in which the Ln(III) atoms adopt a nine-coordinate {LnO(9)} sphere due to their larger ionic radii, whereas the Ln(III) centers in the one-dimensional double-stranded chains of 7-11 with smaller ionic radii lie in a {LnO(8)} coordination environment. In addition, the tunable emission intensity was realized on 7 by controlling the type of the involved counterion on the basis of a reversible solid-state anion exchange. Such reversible solid-state anion exchange might provide an alternative approach to tuning the luminescence.
引用
收藏
页码:2416 / 2426
页数:11
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