期刊文献+

Hydrothermal Reaction, Structure and Magnetic Properties of a Binuclear Cobalt Complex with N-donor Ligand:2-Methyldipyrido[3,2-f:2ˊ3ˊ-h]quinoxaline 被引量:2

Hydrothermal Reaction, Structure and Magnetic Properties of a Binuclear Cobalt Complex with N-donor Ligand:2-Methyldipyrido[3,2-f:2ˊ3ˊ-h]quinoxaline
下载PDF
导出
摘要 One complex [Co1.5(C6H5CHCHCOO)3(Medpq)]·H2O(C6H5CHCHCOO = cinnamic acid, Medpq = 2-methyldipyrido[3,2-f:2,3-h]quinoxaline) 1 has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectrum, TG, single-crystal X-ray diffraction and magnetic susceptibility measurements. Complex 1 crystallizes in the triclinic system, space group P1, with a = 10.224(5), b = 14.572(5), c = 15.139(5)A, α = 112.704(5), β = 97.168(5), γ = 109.749(5), V = 1871.8(13) 3 and Z = 2(at 293(2) K). In the crystal structure, the Co(1) ion is hexa-coordinated with six atoms from three different cinnamic acid ligands and the symmetric three different cinnamic acid ligands; the Co(2) center adopts a coordination environment with two nitrogen atoms from Medpq ligand and four oxygen atoms from two different cinnamic ligands, assuming a slightly distorted octahedral geometry, respectively. The negative value of the Weiss constant indicates antiferromagnetic exchange interactions between the Co ions. One complex [Co1.5(C6H5CHCHCOO)3(Medpq)]·H2O(C6H5CHCHCOO = cinnamic acid, Medpq = 2-methyldipyrido[3,2-f:2,3-h]quinoxaline) 1 has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectrum, TG, single-crystal X-ray diffraction and magnetic susceptibility measurements. Complex 1 crystallizes in the triclinic system, space group P1, with a = 10.224(5), b = 14.572(5), c = 15.139(5)A, α = 112.704(5), β = 97.168(5), γ = 109.749(5), V = 1871.8(13) 3 and Z = 2(at 293(2) K). In the crystal structure, the Co(1) ion is hexa-coordinated with six atoms from three different cinnamic acid ligands and the symmetric three different cinnamic acid ligands; the Co(2) center adopts a coordination environment with two nitrogen atoms from Medpq ligand and four oxygen atoms from two different cinnamic ligands, assuming a slightly distorted octahedral geometry, respectively. The negative value of the Weiss constant indicates antiferromagnetic exchange interactions between the Co ions.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2014年第11期1580-1586,共7页 结构化学(英文)
基金 supported by Tonghua Normal University field project(No.201402)
关键词 cobalt complex magnetic susceptibility measurement 2-methyldipyrido[3 2-f:2ˊ 3ˊ-h]quinoxaline cobalt complex,magnetic susceptibility measurement,2-methyldipyrido[3,2-f:2ˊ,3ˊ-h]quinoxaline
  • 相关文献

参考文献23

  • 1Han, Z. B.; Cheng, X. N.; Chen, X. M. Effect of the size of aromatic chelate ligands on the frameworks of metal dicarboxylate polymers: from helical chains to 2D networks. J. Co,st. Growth Des. 2005, 5, 695-700.
  • 2Brunsveld, L.; Folmer, B. L B.; Meijer, E. W.; Sijbesma, R. P. Supramolecular polymers. Chem. Rev. Z001, 101,4071-4098.
  • 3Fyfe, M. C. T.; Stoddart, J. F. Synthetic sapramolecular chemistry. J. Acc. Chem. Res. 1997, 30, 393--401.
  • 4Caulder, D. L.; Raymond, R. N. Supermoleeules by design, d. Aec. Chem. Res, 1999, 32, 975-982.
  • 5Pan L.; Liu, H.; Lei, X.; Huang, X.; Olson, D. H.; Tun'o, N. J.; Li, 2. PM-I: a recyclable nanoporous martial suitable for ship-in-bottle synthesis and large hydrocarbon sorption. Angew. Chem. Int. Ed. 2003, 42, 542-546.
  • 6Rowsell, J. L. C.; Millward, A. R.; Park, K. S.; Yaghi, O, M. Hydrogen sorption in funetionalized metal-organic fran eworks. ,/Am. Chem. Soc. 2004, 126, 5666-5667.
  • 7Chae, H. K.; Siberio-Perez, D. Y.; Kim, J.; Go, Y. B.; Eddaoudi, M. A.; Matzger, J.; O'Keeffe, M.; Yaghi, O. M. A route to high surface area, porosity and inclusion of large molecules in crystals. Nature 2004, 427, 523-527.
  • 8Aoyama, Y. Functional organic zeolite analogues. M. Design of Organic Solids. Springer Berlin Heidelberg 1998, 165, 131-161.
  • 9Bassani, D. M.; Darcos, V.; Mahony, S.; Desvergne, J. P. Supramolecular catalysis of olefin [2+ 2] photodimerization. J. Am. Chem. Soc. 2000, 122, 8795-8796.
  • 10Muthuraman. M.; Masse, R.; Nicold, J. F.; Desiraju, G. R. Molecular eomplexation as a design tool in the crystal engineering ofnoneentrosymmetrie structures, ideal orientation of chromophores linked by OH.--O and C-H---O hydrogen bonds for nonlinear optics. Chem. Mater. 2001, 13, 1473-1479.

同被引文献4

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部