Possibility of Some Metals Dissolution in Mixtures of Dimethyl Sulfoxide and Aliphatic Halogen Derivative. Part II. Characteristics of the Metallic Nickel Dissolution Reaction in Binary Organic Mixtures

• Autorzy: Lenarcik B. , Jurek K.
• Języki publikacji: EN

Abstrakty

EN

Nickel can be dissolved at temperature 323 K in binary organic mixtures containing dimethyl sulfoxide and one of halogeno aliphatic derivatives: 1,2-dibromoethane or tribromomethane, 1,1,2,2-tetrabromoethane, tetrabromomethane and hexachloroethane. As a result of dissolution of metallic nickel in binary organic system the octahedral nickel(II) complexes were obtained. Products of the dissolution of metallic nickel were characterized by UV-Vis and IR spectroscopy,MS spectrometry, thermal decomposition and analytical methods.

Słowa kluczowe

EN

nickel oxidation; nickel complexes; UV-Vis spectroscopy; IR spectroscopy; S,O ligands; mass spectrometry

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Polish Journal of Chemistry
• Rocznik: 2005
• Tom: Vol. 79 / nr 10
• Strony: 1605--1613
• Opis fizyczny: Bibliogr. 24 poz., rys.

Twórcy

autor

Lenarcik B.

• Department of Inorganic Chemistry, University of Technology and Agriculture, Seminaryjna Str. 3, 85-326 Bydgoszcz, Poland

autor

Jurek K.

• Department of Inorganic Chemistry, University of Technology and Agriculture, Seminaryjna Str. 3, 85-326 Bydgoszcz, Poland

Bibliografia

• 1.Lavrentiev I.P. and Khidckcl M.L., Usp. Khim., 52 596 (1983).
• 2.Tezuka Y., Miya M., Hashimoto A. and Imai K,.,J. Chem. Soc., Chem. Commun., 1642 (1987).
• 3.Gamovski A.D., Kharisov B.I., Gokhon-Zorrilla G. and Gamovski D.A., Usp. Khim., 64, 215 (1995).
• 4.Gutman V., The Donor-Acceptor Approach to Molecular Interactions, Plenum Press, New York, 1978, pp. 121-128.
• 5.Lenarcik B. and Jurek K., Polish J. Chem., 73, 1423 (1999).
• 6.Dombek T., Dolan E. and Schultz J., Environ. Poll., 111,21 (2001).
• 7.Janda V., Vasck P., Bizova J. and Belohlav Z., Chemosphere, 54, 917 (2004).
• 8.Cheng S.-F. and Wu S.-C., Chemosphere, 41, 1263 (2000).
• 9.De Jong V. and Louw R., Appl. Catal. A. 271, 153 (2004).
• 10.Inada Y., Hayashi H., Sugimoto K. and Funabashi S.,.J. Phys. Chem A, 103, 1401 (1999).
• 11.Lever A.B.P., Inorganic Electronic Spectroscopy, Elsevier, New York, (1984) pp. 507-511.
• 12.Cotton F.A., Francis R. and Horroks W.D., J. Phys. Chem.. 64, 1534 (1960).
• 13.Bayari S., Kantarci Z. and Akyuz S., J. Mol. Struct., 351, 19 (1995).
• 14.Farmer P.J., Solouki T., Mills D.K., Soma T., Russell D.H., Reibenspies J.H. and Darensbourg M.Y., J. Am. Chem. Soc., 114,4601 (1992).
• 15.Jurek K.., Ph. D. Thesis, Department of Chemical Technology, University of Technology, Poznan 2003, (in Polish).
• 16.Cecconi F., Ghilardi C.A., Gili P., Midollini S., Luis P.A.L., Lozano-Gorrin A.D. and Orlandini A., Inorg. Chim. Acta, 319, 967 (2001).
• 17.Prasad R. and Kumar A., Thermochim. Acta, 383, 59 (2002).
• 18.Buonomo R.M., Font I., Maguire M.J., Reibenspies J.H., Tuntulani T. and Darensbourg M.Y., J. Am. Chem. Soc., 117, 963 (1995).
• 19.Groenewold G.S., Appelhans A.D., Gresham G.L., Ingram J.C. and Shaw A.D., Int. J. Mass Spectrom., 178, 19(1998).
• 20.Sengottuvelan N., Manonmani J. and Kandaswamy M., Polyhedron, 21, 2767 (2002).
• 21.Grant G.J., Jones M.W., Loveday K.D., Van Derveer D.G., Pennngton W.T., Eagle C.T. and Mehne L.F., Inorg. Chim. Acta, 300, 250 (2000).
• 22.Arquero A., Mendiola M.A., Souza P. and Sevilla M.T., Polyhedron, 15, 1657 (1996).
• 23.Canadas A., Lopez-Torres E., Martinez-Arias A., Mendiola M.A. and Sevilla M.T., Polyhedron, 19, 2059 (2000).
• 24.Marquez V.E. and Anacona J.R., Polyhedron, 16, 1931 (1997).