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Template Synthesis of Sn(II), Sn(IV) and Co(II) complexes via 3-Aminopropyltriethoxysilane and Salicylaldehyde and Evaluate their Antibacterial Sensitivity
Corresponding Author(s) : Hayder Hamied Mihsen
Asian Journal of Chemistry,
Vol. 30 No. 10 (2018): Vol 30 Issue 10, 2018
Abstract
Template method reaction of SnCl2·2H2O or SnCl4·5H2O or CoCl2·6H2O with 3-aminopropyltriethoxysilane and salicyaldehyde have been carried out to prepare three metal complexes; C32H53N2O8ClSnSi2 (A), C32H53N2O8Cl3SnSi2 (B) and C32H52N2O8CoSi2 (C). The prepared metal complexes were characterized by analytical techniques viz., FT-IR, 1H NMR, UV-visible, CHNS elemental and molar conductivity. The analytical data shows that the metal ion to ligand (Schiff base ) ratio in the prepared complexes was in 1:2. Octahedral structures were proposed for A and B complexes while C complex has a tetrahedral structure. The antibacterial activity of metal complexes were investigated against Streptococcus pneumoniae (Gram-negative) and Proteus (Gram-positive). The results showed that all the prepared complexes diminished the bacterial growth.
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- D. Pawlica, M. Marszalek, G. Mynarczuk, L. Sieroñ and J. Eilmes, New J. Chem., 28, 1615 (2004); https://doi.org/10.1039/B409298H.
- J.-P. Costes, F. Dahan, M.B. Fernandez Fernandez, M.I. Fernandez Garcia, A.M. Garcia Deibe and J. Sanmartin, Inorg. Chim. Acta, 274, 73 (1998); https://doi.org/10.1016/S0020-1693(97)05991-4.
- M.T. Kaczmarek, R. Jastrzab, E. Holderna-Kedzia and W. RadeckaParyzek, Inorg. Chim. Acta, 362, 3127 (2009); https://doi.org/10.1016/j.ica.2009.02.012.
- P. Mukherjee, O. Sengupta, M.G. Drew and A. Ghosh, Inorg. Chim. Acta, 362, 3285 (2009); https://doi.org/10.1016/j.ica.2009.02.041.
- M.A. Neelakantan, F. Rusalraj, J. Dharmaraja, S. Johnsonraja, T. Jeyakumar and M. Sankaranarayana Pillai, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 1599 (2008); https://doi.org/10.1016/j.saa.2008.06.008.
- C.E. Housecroft and A.G. Sharpe, Inorganic Chemistry, Pearson Education Limited, Edinburgh Gate Harlow Essex: England, edn 4 (2012,).
- A. Befekadu, M.Sc. Thesis, Synthesis and Characterization of Cu(II) and Ni(II) Schiff Base Complexes Derived from 2-Hydroxyphenyl Oxoacetaldehyde and Ethylenediamine, Haramaya University, Ethiopia (2013).
- F. Diederich and P.J. Stang, Templated Organic Synthesis, Wiley-VCH, Weinheim (1999).
- S. Manju, Ph.D. Thesis, Transition Metal Complexes of Quinoxaline Based Schiff Base Ligands: Synthesis, Characterization and Catalytic Activity Study, Cochin University of Science & Technology, Kochi, India (2010).
- I. Masih, N. Fahmi and Rajkumar, J. Enzyme Inhib. Med. Chem., 28, 33 (2013); https://doi.org/10.3109/14756366.2011.625022.
- A.R. Cutler, C.S. Alleyne and D. Dolphin, Inorg. Chem., 24, 2276 (1985); https://doi.org/10.1021/ic00208a030.
- D.P. Singh, R. Kumar and J. Singh, Eur. J. Med. Chem., 44, 1731 (2009); https://doi.org/10.1016/j.ejmech.2008.03.007.
- E.F. Murphy, L. Schmid, T. Bürgi, M. Maciejewski, A. Baiker, D. Günther and M. Schneider, Chem. Mater., 13, 1296 (2001); https://doi.org/10.1021/cm001187w.
- J.A. Gharamaleki, F. Akbari, A. Karbalaei, K.B. Ghiassi and M.M. Olmstead, Open J. Inorg. Chem., 6, 76 (2016); https://doi.org/10.4236/ojic.2016.61005.
- C. Joubert, M.Sc. Thesis, Heterogenization of Schiff Base Complexes on Mesoporous Silica and their Application as Catalysts in the Oxidative Transformation of Alcohols, Stellenbosch University, Stellenbosch, South Africa (2012).
- E.F. Murphy, D. Ferri, A. Baiker, S. Van Doorslaer and A. Schweiger, Inorg. Chem., 42, 2559 (2003); https://doi.org/10.1021/ic020298p.
- K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds Part A: Theory and Applications in Inorganic Chemistry, John Wiley & Sons, Inc., edn 6 (2009).
- I.S. Ahmed and M.A. Kassem, Spectrochim. Acta A Mol. Biomol. Spectrosc., 77, 359 (2010); https://doi.org/10.1016/j.saa.2010.03.026.
- A.B.P. Lever, Inorganic Electronic Spectroscopy, Elsevier Publishing Company: Amsterdam-London-NewYork (1968).
- W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0.
- O.O. Agarry, F.A. Akinyosoye and F.C. Adetuyi, Afr. J. Biotechnol., 4, 627 (2005); https://doi.org/10.5897/AJB2005.000-3114.
- C. Saxena and R.V. Singh, Adv. Synth. Catal., 336, 707 (1994); https://doi.org/10.1002/prac.19943360815.
- K.A.K. Mohammed, H.M. Abdulkadhim and S.I. Noori, Int. J. Curr. Microbiol. Appl. Sci., 5, 483 (2016); https://doi.org/10.20546/ijcmas.2016.502.054.
References
D. Pawlica, M. Marszalek, G. Mynarczuk, L. Sieroñ and J. Eilmes, New J. Chem., 28, 1615 (2004); https://doi.org/10.1039/B409298H.
J.-P. Costes, F. Dahan, M.B. Fernandez Fernandez, M.I. Fernandez Garcia, A.M. Garcia Deibe and J. Sanmartin, Inorg. Chim. Acta, 274, 73 (1998); https://doi.org/10.1016/S0020-1693(97)05991-4.
M.T. Kaczmarek, R. Jastrzab, E. Holderna-Kedzia and W. RadeckaParyzek, Inorg. Chim. Acta, 362, 3127 (2009); https://doi.org/10.1016/j.ica.2009.02.012.
P. Mukherjee, O. Sengupta, M.G. Drew and A. Ghosh, Inorg. Chim. Acta, 362, 3285 (2009); https://doi.org/10.1016/j.ica.2009.02.041.
M.A. Neelakantan, F. Rusalraj, J. Dharmaraja, S. Johnsonraja, T. Jeyakumar and M. Sankaranarayana Pillai, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 1599 (2008); https://doi.org/10.1016/j.saa.2008.06.008.
C.E. Housecroft and A.G. Sharpe, Inorganic Chemistry, Pearson Education Limited, Edinburgh Gate Harlow Essex: England, edn 4 (2012,).
A. Befekadu, M.Sc. Thesis, Synthesis and Characterization of Cu(II) and Ni(II) Schiff Base Complexes Derived from 2-Hydroxyphenyl Oxoacetaldehyde and Ethylenediamine, Haramaya University, Ethiopia (2013).
F. Diederich and P.J. Stang, Templated Organic Synthesis, Wiley-VCH, Weinheim (1999).
S. Manju, Ph.D. Thesis, Transition Metal Complexes of Quinoxaline Based Schiff Base Ligands: Synthesis, Characterization and Catalytic Activity Study, Cochin University of Science & Technology, Kochi, India (2010).
I. Masih, N. Fahmi and Rajkumar, J. Enzyme Inhib. Med. Chem., 28, 33 (2013); https://doi.org/10.3109/14756366.2011.625022.
A.R. Cutler, C.S. Alleyne and D. Dolphin, Inorg. Chem., 24, 2276 (1985); https://doi.org/10.1021/ic00208a030.
D.P. Singh, R. Kumar and J. Singh, Eur. J. Med. Chem., 44, 1731 (2009); https://doi.org/10.1016/j.ejmech.2008.03.007.
E.F. Murphy, L. Schmid, T. Bürgi, M. Maciejewski, A. Baiker, D. Günther and M. Schneider, Chem. Mater., 13, 1296 (2001); https://doi.org/10.1021/cm001187w.
J.A. Gharamaleki, F. Akbari, A. Karbalaei, K.B. Ghiassi and M.M. Olmstead, Open J. Inorg. Chem., 6, 76 (2016); https://doi.org/10.4236/ojic.2016.61005.
C. Joubert, M.Sc. Thesis, Heterogenization of Schiff Base Complexes on Mesoporous Silica and their Application as Catalysts in the Oxidative Transformation of Alcohols, Stellenbosch University, Stellenbosch, South Africa (2012).
E.F. Murphy, D. Ferri, A. Baiker, S. Van Doorslaer and A. Schweiger, Inorg. Chem., 42, 2559 (2003); https://doi.org/10.1021/ic020298p.
K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds Part A: Theory and Applications in Inorganic Chemistry, John Wiley & Sons, Inc., edn 6 (2009).
I.S. Ahmed and M.A. Kassem, Spectrochim. Acta A Mol. Biomol. Spectrosc., 77, 359 (2010); https://doi.org/10.1016/j.saa.2010.03.026.
A.B.P. Lever, Inorganic Electronic Spectroscopy, Elsevier Publishing Company: Amsterdam-London-NewYork (1968).
W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0.
O.O. Agarry, F.A. Akinyosoye and F.C. Adetuyi, Afr. J. Biotechnol., 4, 627 (2005); https://doi.org/10.5897/AJB2005.000-3114.
C. Saxena and R.V. Singh, Adv. Synth. Catal., 336, 707 (1994); https://doi.org/10.1002/prac.19943360815.
K.A.K. Mohammed, H.M. Abdulkadhim and S.I. Noori, Int. J. Curr. Microbiol. Appl. Sci., 5, 483 (2016); https://doi.org/10.20546/ijcmas.2016.502.054.