Two novel hybrid compounds based on [MW12O40]5- (M = B, Al) heteropolyanions and copper coordination polymer with bpp ligands

被引:17
作者
Chen, Ying [1 ]
Zhou, Baibin [1 ]
Zhao, Jingxiang [1 ]
Li, Yangguang [2 ]
Su, Zhanhua [1 ]
Zhao, Zhifeng [1 ]
机构
[1] Harbin Normal Univ, Key Lab Phys & Chem Mat, Coll Heilongjiang Prov, Harbin 150025, Peoples R China
[2] NE Normal Univ, Key Lab Polyoxometalate Sci, Minist Educ, Fac Chem, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Keggin-type polyoxometalate; Group; 13; element; Transition-metal complex; Flexible ligand; Electrochemical property; KEGGIN-TYPE POLYOXOMETALATE; HYDROTHERMAL SYNTHESES; CRYSTAL-STRUCTURES; CLUSTERS; CHANNELS; ALPHA;
D O I
10.1016/j.ica.2010.07.060
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Under hydrothermal condition, two novel organic-inorganic hybrid compounds, [Cu(bpp)][Cu-2.5(bpp)(3)-( Hbpp)]H-0.5[BW12O40]center dot 1.5H(2)O (1) and [Cu(en)(2)(H2O)]{[Cu(bpp)](3)[AlW12O40]}center dot H2O (2) (bpp = 1,3-bis(4-pyridyl) propane; en = ethylenediamine), have been synthesized based on B/Al atom-centered Keggin-type polyoxometalates combined with Cu ions and bpp ligands. The two compounds are characterized through single-crystal X-ray diffraction analysis, elemental analyse, IR, UV and TG. For compound 1, as the nodes, the [BW12O40](5) polyanions link to the [Cu-2.5(bpp)(3)(Hbpp)](3.5+) oligomers, leading to the formation of 1D helical chains which further attach to the macrocycles [Cu-2(bpp)(2)](2+) via the Cu-O weak interaction to construct the 2D "wave-like" layers. For compound 2, the {[Cu(bpp)](4)[AlW12O40](2)} unit is obtained by the interaction between two Keggin-type [AlW12O40](5) polyanions and one tetranuclear macrocycle composed by four [Cu(bpp)](+) complex cations. Furthermore, the units are sandwiched by two 1D "wave-like" polymeric chains resulting in a new 1D structure. In addition, the electrochemical properties and electrocatalytic activities of these two compounds have been studied in this paper. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:3897 / 3903
页数:7
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