Two Cobalt(II) Coordination Polymers Based on Tetrazylphosphonate and Tetrazylphosphonic Acid Ligands

被引:0
|
作者
Zhao Yu-Chun [1 ]
Yao Lin-Shan [1 ]
Li Jian-Yue [1 ]
Yu Ying-Hui [1 ,2 ]
Hou Guang-Feng [2 ]
Gao Jin-Sheng [1 ,2 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China
[2] Heilongjiang Univ, Engn Res Ctr Pesticide, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
Co(II) complex; crystal structure; coordination polymer; magnetic property; METAL-ORGANIC FRAMEWORKS; MAGNETIC-PROPERTIES; COMPLEXES; DIPHOSPHONATES; LUMINESCENT;
D O I
10.14102/j.cnki.0254-5861.2011-1308
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two cobalt coordination polymers with the same 2D structure have been hydrothermally synthesized based on two bifunctional ligands with tetrazole and phosphonate (phosphonic acid) groups, namely, diethyl 4-(2H-1,2,3,4-tetrazol-5-yl) benzylphosphonate (C2H5-L1) and 4-(2H-1,2,3,4-tetrazol-5-yl) benzylphosphonic acid (H(2)L2). The structures of the two complexes are characterized by elemental analysis, IR, TGA and X-ray single-crystal/powder diffraction. The pink block crystals of complex [Co(L1)(H2O)]center dot H2O (1) belong to the monoclinic system, space group C2/m with a = 20.8390(11), b = 7.2695(3), c = 10.0156(6) angstrom, beta = 109.773(7)degrees, V = 1427.80(13)angstrom(3), Z = 4, D-c = 1.680 mg/cm(-3), M-r = 361.16, F(000) = 740, R = 0.0316 and wR = 0.0826 for 1702 observed reflections (I > 2 sigma(I)). The purple block crystals of complex [Co(L2)(H2O)]center dot 2H(2)O (2) also belong to the monoclinic system, space group C2/c with a = 25.5382(16), b = 7.3844(3), c = 15.1925(11) angstrom, beta = 124.238(9)degrees, V = 2368.6(2)angstrom(3), Z = 8, D-c = 1.969 mg/cm(-3), M-r = 351.12, F(000) = 1432, R = 0.0475, wR = 0.1617 for 2088 observed reflections (I > 2 sigma(I)). Both the nitrogen atoms of tetrazole group and oxygen atoms of phosphonate (phosphonic acid) groups in the ligands coordinated with the metal cobalt. The magnetic property of complex 1 is also investigated.
引用
收藏
页码:453 / 462
页数:10
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