Cationic bipy induced the three dimensional supramolecules based on azoxybenzene tetracarboxylate: Structures and NIR luminescence property

被引:21
作者
Feng, Xun [1 ,2 ]
Chen, Haipeng [1 ,2 ]
Li, Rongfang [1 ,2 ]
Yang, Mingting [1 ,2 ]
Guo, Shilei [1 ,2 ]
Wang, Liya [3 ]
Liang, Qingru [1 ,2 ]
Li, Zhongjun [4 ]
机构
[1] Luoyang Normal Univ, Coll Chem & Chem Engn, Luoyang 471934, Peoples R China
[2] Luoyang Normal Univ, Henan Key Lab Funct Oriented Porous Mat, Luoyang 471934, Peoples R China
[3] Nanyang Normal Univ, Sch Life Sci & Technol, Nanyang 473601, Peoples R China
[4] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Lanthanide(III)-organic based compounds; Chemical modification; Near-infrared luminescence; Azoxybenzene tetracarboxylic acid; Fluorescence lifetime; METAL-ORGANIC FRAMEWORKS; COORDINATION POLYMERS; COMPLEXES; SERIES; TOPOLOGY; ACID; MOFS; HO;
D O I
10.1016/j.poly.2018.10.055
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Series of Ln(III) coordination polymers, namely, {[Ln(Oaobtc)(H2O)(4)]center dot Hbipy center dot H2O}(n)(H(4)Oaobtc = oxidation azoxybenzene - 2, 2', 3, 3'-tetracarboxylic acid, bipy = 4,4'-bipyridine, and Ln = Pr(1), Nd(2), Ho(3), Er (4), Yb(5), respectively) have been designed, afforded and luminescence characterized systematically. The family coordination polymers are nearly isostructural sets, featuring one dimensional (1D) zigzag double chain edifice structure, with cationic Hbipy(+) guest being located along two sides. These 1D chains are interlinked into 2D network, and are further extended into 3D supramolecular architecture through hydrogen bonding interactions from the cationic Hbipy(+) moiety. The photo luminescence emission spectra of polymer 1 and 4 are based on the H(4)aobtc acid ligand, while 2, 3 and 5 display the emissions originated from characteristic f-f transitions of Ln(III) ions within near-infrared (NIR) regions. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:420 / 427
页数:8
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