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Hydrothermal Synthesis and Structure of a Novel Coordination Polymer Co_3(tma)(pda)_2(H_2O)_3]n·nH_2O 被引量:1

Hydrothermal Synthesis and Structure of a Novel Coordination Polymer Co_3(tma)(pda)_2(H_2O)_3]n·nH_2O
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摘要 A novel coordination polymer [Co3(tma)(pda)2(H2O)3]n·nH2O was synthesized by hydrothermal reaction of 3-(3-pyridyl)acrylate acid (pda) and trimesic acid (tma) with COCl2·6H2O. The structure was characterized by elemental analysis, IR spectroscopy and X-ray single-crystal diffraction analysis. It crystallizes in triclinic, space group PT with a = 9.569(4), b = 12.562(6), c = 12.666(6) A, a = 97.321(7), β = 110.295(7), γ = 106.110(7)°, V = 1328.9(10)A^3, Dc = 1.877 g/cm^3, Mr = 751.24, Z = 2,μ = 1.930 mm^-1, F(000) = 758, the final R = 0.0392 and wR = 0.0837. The diffraction result shows that Co atoms are linked through pda and tma ligands to form an infinite three-dimensional network. A novel coordination polymer [Co3(tma)(pda)2(H2O)3]n·nH2O was synthesized by hydrothermal reaction of 3-(3-pyridyl)acrylate acid (pda) and trimesic acid (tma) with COCl2·6H2O. The structure was characterized by elemental analysis, IR spectroscopy and X-ray single-crystal diffraction analysis. It crystallizes in triclinic, space group PT with a = 9.569(4), b = 12.562(6), c = 12.666(6) A, a = 97.321(7), β = 110.295(7), γ = 106.110(7)°, V = 1328.9(10)A^3, Dc = 1.877 g/cm^3, Mr = 751.24, Z = 2,μ = 1.930 mm^-1, F(000) = 758, the final R = 0.0392 and wR = 0.0837. The diffraction result shows that Co atoms are linked through pda and tma ligands to form an infinite three-dimensional network.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第1期49-52,共4页 结构化学(英文)
基金 ThisworkwassupportedbytheNaturalScienceFoundationofHebeiprovince(B2005000534)
关键词 coordination polymer hydrothermai synthesis crystal structure coordination polymer, hydrothermai synthesis, crystal structure
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  • 1Liu, S. Z., Li, J. P., Zhang, Z. W., Chen, J. Y., Xing, Y., Jia, It. Q., Lin, Y. H., Chinese J. Struct. Chem. 2001, 20, 221-225.
  • 2Zeng, Q. X., Yang, G. Y., Xu, J. Q., Huang, X. Y. Chinese J. Struct. Chem. 2003, 22, 103-108.
  • 3Zeng, X. R., Xiong, R. G., You, X. Z. Wuji Huaxue Xuebao 2000, 16, 641-646.
  • 4Ayyappan, P., Evans, O. R., Lin, W.Inorg. Chem. 2001, 40, 4627-4632.
  • 5Liu, Y. H., Lin, C. S., Chen, S. Y., Tsai, H. L., Ueng, C. H., Lu, K. L. J. Solid State. Chem. 2001, 157, 166-172.
  • 6Bu, X. H., Liu, H., Du, M., Zhang, L., Guo, Y. M., Shionoya, M., Ribas, J.Inorg. Chem. 2002, 41, 1855-1861.
  • 7Yang, W., Lu, C., Lin, X., Wu, C., Wu, D., Zhuang, H.Inorg. Chem. Commun. 2001, 4, 285-289.
  • 8Lin, Z. Z., Zhang, H. H., Huang, C. C., Sun, R. Q. Chinese J. Struct. Chem. 2002, 21, 42-45.
  • 9Sheldrick, G. M. SADABS: Program for Empirical Absorption Correction of Area Detector Data, University of Gottingen, Germany 1996.
  • 10Sheldrick, G. M. SHELXTL: Structure Determination Software Programs, Bruker Analytical X-ray System, Inc., Madison, W, USA 1997.

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