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Hydrothermal Synthesis, Crystal Structure and EPR Property of Tetranuclear Copper(II) Cluster [Cu4OCl6(C14H12N2)4]

  • Jian, Fang-Fang (New Materials & Function Coordination Chemistry Laboratory, Qingdao University of Science and Technology) ;
  • Zhao, Pu-Su (Materials Chemistry Laboratory, Nanjing University of Science and Technology) ;
  • Wang, Huan-Xiang (New Materials & Function Coordination Chemistry laboratory, Qingdao University of Science and Technology) ;
  • Lu, Lu-De (Materials Chemistry Laboratory, Nanjing University of Science and Technology)
  • Published : 2004.05.20

Abstract

The tetranuclear copper(II) cluster compound $[Cu_4OCl_6(C_{14}H_{12}N_2)_4]$ has been synthesized by hydrothermal reaction and studied by X-ray diffraction. The four copper(II) atoms locate four capsheaves of a tetrahedral skeletal structure and a oxygen atom as interstitial atom occupies the center position of the same tetrahedron, and each edge of the Cu-Cu tetrahedron is bridged by one ${\mu}_2$-Cl anion. The copper atom possesses slightly distorted trigonal bipyramidal geometry with three ${\mu}_2$-Cl atoms in equatorial position and the interstitial O atom and one N atom from 3-benzyl-benzimidazole ligand occupying axial position. The Cu-Cu distances are in the range of 3.0986-3.1162 ${\AA}$. The EPR spectrum suggested that the copper(II) ground state $d_{x2-y2}$ and the coordination geometry was trigonal bipyramidal.

Keywords

References

  1. Sakai, T.; Hamada, T.; Awata, N.; Watanabe, J. Pharmacobio.Dyn. 1989, 12, 530. https://doi.org/10.1248/bpb1978.12.530
  2. Brown, H. D.; Matzuk, A. R.; Ilves, I. R.; Peterson, L. H.; Harris,S. A.; Sarett, L. H.; Egerton, J. R.; Yakstis, J. J.; Campbell, W. C.;Cuckler, A. C. J. Am. Chem. Soc. 1961, 83, 1764. https://doi.org/10.1021/ja01468a052
  3. Preston, P. N. Chem. Rev. 1974, 74, 279. https://doi.org/10.1021/cr60289a001
  4. Bouwman, E.; Driessen, W. L.; Reedijk, J. Coord. Chem. Rev.1990, 104, 143. https://doi.org/10.1016/0010-8545(90)80042-R
  5. Pujar, M. A.; Bharamgoudar, T. D.; Sathyanarayana, D. N.Transition Met. Chem. 1988, 13, 423. https://doi.org/10.1007/BF01043702
  6. O'Sullivan, D. G.; Wallis, A. K. J. Med. Chem. 1972, 15, 103. https://doi.org/10.1021/jm00271a032
  7. Mylonas, S.; Valavanidis, A.; Dimitropoulos, K.; Polissiou, M.;Tsiftsoglou, A. S.; Viziranakis, I. S. J. Inorg. Biochem. 1988, 34,265. https://doi.org/10.1016/0162-0134(88)83004-6
  8. Bei, F. L.; Jian, F. F.; Lu, L. D.; Yang, X. J.; Wang, X. ActaCryst. 2000, C56, 718.
  9. Jian, F. F.; Bei, F. L.; Yang, X. J.; Lu, L. D.; Wang, X. Acta Cryst. 2001, C57, 176.
  10. Bei, F. L.; Jian, F. F.; Yang, X. J.; Lu, L. D.; Wang, X. Acta Cryst. 2001, C57, 45.
  11. Bertrand, J. A.; Kelly, J. A. J. Am. Chem. Soc. 1966, 88, 4746. https://doi.org/10.1021/ja00972a053
  12. Bertrand, J. A.; Kelly, J. A. Inorg. Chem. 1969, 9, 1982.
  13. Gill, N. S.; Sterns, M. Inorg. Chem. 1970, 9, 619. https://doi.org/10.1021/ic50085a037
  14. Dickinson, R. C.; Helm, F. T.; Baker, A.; Black, T. D.; Watson, D. H. Inorg.Chem. 1977, 16, 1530. https://doi.org/10.1021/ic50172a058
  15. Drake, R. F.; Crawford, V. H.; Hatfield, W. J. Chem. Phys. 1974,60, 4525. https://doi.org/10.1063/1.1680934
  16. Norman, R. E.; Rose, N. J.; Stenkamp, R. E. Acta Cryst. 1989,C45, 1707.
  17. Atria, A. M.; Vega, A.; Contreras, M.; Valenzuela, J.; Spodine, E.Inorg. Chem. 1999, 38, 5681. https://doi.org/10.1021/ic990389v
  18. Jones, D. H.; Sams, J. R.; Thompson, R. C. J. Chem. Phys. 1983,79, 3877. https://doi.org/10.1063/1.446254
  19. Sheldrick, G. M. SAINT V4 Software Reference Manual; SiemensAnalytical X-ray Systems, Inc.: Madison Wisconsin, USA, 1996.
  20. Sheldrick, G. M. SADABS. Program for Empirical AbsorptionCorrection of Area Detector Data; University of Gottingen:Germany, 1996.
  21. Sheldrick, G. M. SHELXTL97, Program for Crystal StructureRefinement of Crystal Structures; University of Göttingen:Germany, 1997.
  22. Rowland, J. M.; Thornton, M. L.; Olmstead, M. M.; Mascharak, P.K. Inorg. Chem. 2001, 40, 1069. https://doi.org/10.1021/ic000848o
  23. Fang, C. J.; Duan, C. Y.; Guo, D.; He, C.; Meng, Q. J.; Wang, Z.M.; Yan, C. H. Chem. Commun. 2001, 2540.
  24. Hathaway, B. J.; Tomlinson, A. A. G. Coord. Chem. Rev. 1970, 5, 1. https://doi.org/10.1016/S0010-8545(00)80073-9
  25. Hathaway, B. J. J. Chem. Soc., Dalton Trans. 1972, 1196.

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