Coordination site induced controllable assembly of metal-organic units in polyoxometalate-based hybrids

被引:6
|
作者
Dong, Huan [1 ,2 ]
Yang, Yanan [1 ,2 ]
Zhao, Fangfang [1 ,2 ]
Ji, Wenbin [1 ,2 ]
Liu, Beibei [1 ,2 ]
Hu, Hailiang [1 ,2 ]
Wang, Yang [3 ]
Huang, Hui [1 ,2 ]
Liu, Yang [1 ,2 ]
Kang, Zhenhui [1 ,2 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215123, Peoples R China
[3] Liaoning Univ, Coll Pharm, Shenyang 110036, Peoples R China
基金
中国国家自然科学基金;
关键词
Coordination site; Polyoxometalate; Metal-organic unit; FRAMEWORKS; CLUSTERS; CHAINS;
D O I
10.1016/j.inoche.2014.03.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two hybrid materials based on Keggin-type polyoxometalate, [Ag-4(mtrz)(4)(H2O)(2)(SiW12O40)] (1), [Ag-4(mtez)(5) (SiW12O40)] center dot H2O (2), (mtrz = 1-methyl-1,2,4-triazole, mtez = 1-methyl-1,2,3,4-tetrazole), have been hydrothermally synthesized and structurally characterized. Through the use of the azole ligands mtrz and mtez, compounds 1 and 2 with totally different metal-organic units are obtained. In 1, the mtrz ligands with N atoms in meta-positions induced the formation of chain-like metal-organic units, while in 2, the mtez ligands with adjacent N atoms induced the assembly of tetranuclear units. The SiW12 anions act as bridging linkers to evolve the structural dimensionality of the two title compounds into 20 network and 3D framework, respectively. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:107 / 110
页数:4
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