The synthesis of some organotin (IV) compounds in the melt- phase
محورهای موضوعی : Journal of the Iranian Chemical ResearchUche B. Eke 1 , Temitope O. Abodunrin 2 , Samson O. Owalude 3
1 - Department of Chemistry, University of Ilorin, PMB 1515, Ilorin, Nigeria
2 - Department of Chemistry, University of Ilorin, PMB 1515, Ilorin, Nigeria
3 - Department of Chemistry, University of Ilorin, PMB 1515, Ilorin, Nigeria
کلید واژه: Organotin, Melt-phase, Carboxylate group, Benzoic acid,
چکیده مقاله :
The melt-phase synthesis of dioctyltin (IV) and triphenyltin (IV) benzoates were carried outusing stoichiometric amounts of benzoic acids and the corresponding organotin (IV) compounds.The reagents were ground together in a mortar and fed into a boiling glass tube. A cannula tubewas inserted into the boiling tube to discharge accumulated gaseous products. A syringe ensureda continuous flow of dry Nitrogen gas in the reaction vessel. The compounds are known usingwet Chemistry. Their syntheses via the melt-phase were in good yields. The physical propertiescorresponded to those of the similar compounds prepared by wet chemistry. The IR, 1H and 13CNMR data indicate that coordination to the tin atom is via carboxylate group.
[1] B. Gyuresik, I. Nagy, Coord. Chem. Rev. 203 (2000) 81-149.
[2] Y. Farina, A. Graisa, M. Kassem, E. Yousif, Eur. J. Sci. Res. 22 (2008) 602-607.
[3] W. Rehman, M.K. Baloch, A. Badshah, S. Ali, J. Chin. Chem. Soc. 52 (2005) 231-236.
[4] M. Nath, S. Pokharia, R. Yadav, Coord. Chem. Rev. 215 (2001) 99-149.
[5] M. Gielen, Applied Organomet. Chem. 16 (2002) 481-494.
[6] W. Rehman, M.K. Balaoch, A. Badshah, J. Braz. Chem. Soc. 16 (2005) 827-834.
[7] M.H. Bhatti, S. Ali, F. Huma, S. Shahzadi, Turk. J. Chem. 29 (2005) 463-476.
[8] K.R. Seddon, J. Chem. Technol. Biotechnol. 68 (1997) 351-356.
[9] S. Wells, J.M. Disimone, Angew. Chem. Int. Ed. 40 (2001) 519-527.
[10] K. Tanaka, F. Toda, Chem. Rev. 100 (2000) 1025-1074.
[11] O.G. Adeyemi, N.J. Coville, Organometallics 22 (2003) 2284-2290.
[12] B. Zewdie, “Synthesis and antimicrobial activity of triphenyltinbenzoate aniline complex”. M.Sc.
Thesis submitted to the School of Graduate Studies of Addis Ababa University, Ethiopia, 2008.
[13] R.R. Holmes, R.O. Day, V. Chandrasekhar, J.F. Vollano, J.M. Holmes, Inorg. Chem. 25 (1986)
2490-2494.
U.B. Eke & et al. / J. Iran. Chem. Res. 3 (2010) 237-243
243
[14] U.B. Eke, N.J. Coville, Inorg. Chem. Commun. 3 (2000) 368-370.
[15] O.G. Adeyemi, U.B. Eke, L. Cheng, M. Cook, D.G. Billing, B.B. Mamba, D.C. Levendis, N.J.
Coville, J. Organomet. Chem. 689 (2004) 2207-2215.
[16] H. Hussain, V.U. Ahmad, I.R. Green, K. Krohn, J. Hussain, A. Badshah, ARKIVOC, xiv (2007)
289-299.
[17] J. Li, G. Zhao, G. Xiong, Y. Ma, Synth. React. Inorg. Met-Org. Chem. 31 (2001) 85-93.
[18] M. Danish, S. Ali, A. Badshah, H.G. Alt, M. Mazhar, N. Islam, J. Organomet. Chem. 486 (1995) 51-
56.
[19] Z.H. Chohan, M. Arif, M.A. Akhtar, C.T. Supuran, Bioinorg Chem. Appl. ID93131 (2006) 1-13.
[20] M. Nath, R. Yadav, Bull. Chem. Soc. Jpn. 71 (1998) 1355-1362.
[21] Z.M. Mei, W. Fang, Acta Cryst. Sect. E 64 (2008) m857-m866.
[22] J.K. Sandhu, R. Gupta, S.S. Sandhu, R.F. Parish, Polyhedron 4 (1985) 81-87.
[23] J.F. Vollano, R.O. Day, D.N. Rau, V. Chandrasekhar, R.R. Holmes, Inorg. Chem. 23 (1984) 3153-
3160.
[24] R.G. Swisher, J.F. Vollano, V. Chandrasekhar, R.O. Day, R.R. Holmes, Inorg. Chem. 23 (1984)
3147-3152.
[25] S. Ahmed, M.H. Bhatti, S. Ali, F. Ahmed, Turk. J. Chem. 30 (2006) 193-202.
[26] M. Nath, S. Goyal, G. Eng, N. Ogawura,. Synth. React. Inorg. Met-Org. Chem. 28 (1998) 1619-
1641.