Four 3d–4d heterometallic coordination polymers based on 1,2,3-triazole-4,5-dicarboxylate: Synthesis, structures, and magnetic properties

Four 3d–4d heterometallic coordination polymers, were synthesized under hydrothermal conditions. The single-crystal X-ray diffraction analysis reveals that complexes 1–3 are isostructural; the complex 4 exhibits a three-dimensional architecture constructed by planar {AgCu4N12} units. •Four novel 3d–...

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Published inInorganica Chimica Acta Vol. 409; pp. 497 - 502
Main Authors Sun, Ya-Guang, Gao, Xin, Xiong, Gang, Zong, Wen-Hui, Ding, Fu, Xu, Zhen-He, Wang, Shu-Ju, You, Li-Xin, Ren, Bao-Yi, Gao, En-Jun
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.01.2014
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Summary:Four 3d–4d heterometallic coordination polymers, were synthesized under hydrothermal conditions. The single-crystal X-ray diffraction analysis reveals that complexes 1–3 are isostructural; the complex 4 exhibits a three-dimensional architecture constructed by planar {AgCu4N12} units. •Four novel 3d–4d coordination polymers have been synthesized.•Compounds 1, 2 and 4 show a strong antiferromagnetic coupling.•The H3TzDC ligand exhibits diverse coordination modes.•The complex 4 shows a 3D architecture constructed by planar {AgCu4N12} units. Four 3d–4d heterometallic coordination polymers, [Ag2M(HTzDC)2·3H2O]n(M=Co(1), Ni(2), Zn(3) and {[(CH3)2NH2][AgCu5(TzDC)4·6H2O]·6H2O]}n(4) (H3TzDC=1,2,3-triazole-4,5-dicarboxylic acid) were synthesized under hydrothermal conditions using one-step approach and structurally characterized by elemental analysis, FT-IR, power X-ray diffraction and single-crystal X-ray diffraction. The single-crystal X-ray diffraction analysis reveals that complexes 1–3 are isostructural, the three dimensional frameworks is composed of Ag ions and transition metals which linked by TzDC ligands; the complex 4 exhibits a three-dimensional architecture constructed by planar {AgCu4N12} units. The magnetic properties of compounds 1–2 and 4 were investigated.
ISSN:0020-1693
1873-3255
DOI:10.1016/j.ica.2013.09.039