Synthesis and Crystal Structure of Two Decavanadates Cluster Metal Complexes: [Co(H2O)6]2[H2V10O28]·6H2O and (NH4)2[Ca(H2O)7]2[V10O28]

Journal of Cluster Science - Tập 20 - Trang 621-627 - 2009
Haixing Liu1,2, Jing Wang3, Fangfang Jian1,3, Hailian Xiao3
1Microscale Science Institute, Weifang University, Weifang, People’s Republic of China
2Department of Chemistry and Chemical Engineering, Weifang University, Weifang, People’s Republic of China
3New Materials and Function Coordination Chemistry Laboratory, Qingdao University of Science and Technology, Qingdao, People's Republic of China

Tóm tắt

Two new decavanadate metal complexes, [Co(H2O)6]2[H2V10O28]·6H2O (1) and (NH4)2[Ca(H2O)7]2[V10O28] (2), have been synthesized under hydrothermal condition by using chlorhydric acid as the initiator at 120 °C. The aqueous NaVO3 solution with an aqueous solution of CoCl2·6H2O were used for generating 1 and aqueous CaCl2·2H2O and NH4VO3 solution were employed for creating 2. Compound 1 consisted of discrete hexa-aqua-cobalt [Co(H2O)6]2+ cations, [H2V10O28]4− anions and non-coordination water molecules. Compound 2 were composed of hepta-aqua-calcium [Ca(H2O)7]2+ cations, ammonium NH4 + and [V10O28]6− anion. For compound 2, the distorted pentagonal bipyramid [Ca(H2O)7]2+ is uncommon. In the crystal lattice, hydrogen bonds played an important role on connecting cations, anions and non-coordinated water molecules to form the three-dimensional network.

Tài liệu tham khảo

M. T. Pope and A. Muller (1991). Angew. Chem. Int. Ed. Engl. 30, 34. J. T. Rhule, C. L. Hill, D. A. Judd, and R. F. Schinazi (1998). Chem. Rev. 98, 327. E. Rakovsky, D. Joniakova, R. Gyepes, P. Schwendt, and Z. Micka (2005). Cryst. Res. Technol. 40(7), 719. Y. Shan and S. D. Huang (1999). J. Chem. Crystallogr. 29(1), 93. S. Sharma, A. Ramanan, P. Y. Zavalij, and M. S. Whittingham (2002). CryEngComm 4(100), 601. R. M. Barrer, Hydrothermal Chemistry of Zeolites (Academic Press, New York, 1982). A. Rabenau (1985). Angew. Chem. Int. Ed. Engl. 24, 1026. G. M. Sheldrick (1969). Acta Crystallogr. Sect. A. 46, 467. G. M. Sheldrick, SHELXTL97, Program for Crystal Structure Refinement (University of Gottingen, Germany, 1993). A.J. Wilson, International Table for X-ray Crystallography, Vol. C (Kluwer Academic Publishers, Dordrecht, 1992), Tables 6.1.1.4, pp. 500–502 and 4.2.6.8, pp. 219–222. S. Nakamura and T. Ozeki (2001). J. Chem. Soc. Dalton Trans. 472. T. Li, J. Lu, S. Gao, F. Li, and R. Cao (2007). Chem. Lett. 36(3), 356. H. Kumagai, M. Arishima, S. Kitagawa, K. Ymada, S. Kawata, and S. Kaizaki (2002). Inorg. Chem. 41, 1989. R. B. Van Dreele and R. C. Fay (1971). J. Am. Chem. Soc. 93, 4936. P. K. Hon and C. E. Pfluger (1973). J. Coord. Chem. 3, 67. L. Martin, S. S. Turner, P. Day, P. Guionneau, J. A. K. Howard, D. E. Hibbs, M. E. Light, M. B. Hursthouse, M. Uruichi, and K. Yakushi (2001). Inorg. Chem. 40, 1363. O. Moers, A. Blaschette, and P. G. Jones (1997). Acta Crystallogr. C53, 845.