Three functional Cd(II) coordination polymers constructed by the thiazolothiazole extended viologen ligand

被引:7
|
作者
Yang, Fengyi [1 ]
Chen, Jiali [1 ]
Fu, Yuying [1 ]
Wang, Junwen [1 ]
Liu, Jinjian [1 ]
机构
[1] Shanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Magnet Mol & Magnet Informat Mat, Minist Educ, Taiyuan 030032, Peoples R China
关键词
Extended viologens; Crystal structure; Photochromism; Photo-controlled fluorescence; Inkless and erasable printing; METAL-ORGANIC FRAMEWORKS; PHOTOCHROMISM;
D O I
10.1016/j.dyepig.2023.111877
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Expanding the pi-conjugated structure of traditional viologens by incorporating thiazole units to the bipyridine skeleton has attracted more and more attention. In this work, a rigid thiazolothiazole extended viologen ligand (TTVP, 2,5-bis (pyridinium-4-yl) thiazolo [5,4-d] thiazole propionate) has been used to constitute three new functional Cd(II) coordination polymers (CPs), {[Cd(TTVP)0.5(HBTC)(H2O)2]center dot 2H2O}n (1), {[Cd(TTVP)0.5(pBDC)0.5(p-HBDC)(H2O)]center dot 3H2O}n (2), {[Cd(TTVP)0.5(m-BDC)]}n (3) by introducing different benzenecarboxylic acids as auxiliary ligands (H3BTC = 1,3,5-benzenetricarboxylic acid; p-H2BDC = 1,4-benzenedicarboxylic acid; m-H2BDC = 1,3-benzenedicarboxylic acid). The crystal structures and photochromic capabilities of 1-3 are studied. Both compounds 1 and 2 own one-dimensional (1D) chain-like structure, while compound 3 owns twodimensional (2D) layered structure. As expected, compounds 1-3 show reversible photochromism due to electron-transfer (ET). In addition, the photo-controlled luminescent properties and the potential application as inkless and erasable printing media are also explored.
引用
收藏
页数:8
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