Copyright (c) 2019 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Spectral Investigations of Polymeric Hydrazone Schiff Base and its Transition Metal Complexes with Promising Antimicrobial, Anti-Angeogenic and DNA Photo-Cleavage Activities
Corresponding Author(s) : Manoj Kumar
Asian Journal of Chemistry,
Vol. 31 No. 10 (2019): Vol 31 Issue 10
Abstract
This report describes the synthesis and exploration of novel Schiff base ligand in the form of a polymer (heptamer) which was prepared by reaction between 3,4-diacetyl-2,5-hexanedione and hydrazine hydrate in ethanol. On further reaction of Schiff base with transition metals ions (Co and Cu) leads to formation of its transition metal complexes. The structural identification of Schiff base ligand and its transition metal complexes were characterized by classical structural techniques like FT-IR, NMR and mass spectra. The free ligand and its transition metal complexes have been screened for in vitro biological activities against various strains of bacteria and fungi. The prepared Schiff base and its metal complexes were also screened for antiangiogenic activity. The results have shown the remarkable antimicrobial and antiangiogenic activities of the Schiff base and its metal complexes.
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- S. Kumar, D.N. Dhar and P.N. Saxena, J. Sci. Ind. Res., 68, 181 (2009).
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References
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H.C. Aspinall, Chem. Rev., 102, 1807 (2002); https://doi.org/10.1021/cr010288q.
K.L. Haas and K.J. Franz, Chem. Rev., 109, 4921 (2009); https://doi.org/10.1021/cr900134a.
T. Rosu, S. Pasculescu, V. Lazar, C. Chifiriuc and R. Cernat, Molecules, 11, 904 (2006); https://doi.org/10.3390/11110904.
S.K. Sridhar, S.N. Pandeya, J.P. Stables and A. Ramesh, Eur. J. Pharm. Sci., 16, 129 (2002); https://doi.org/10.1016/S0928-0987(02)00077-5.
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J.A. Sclafani, M.T. Maranto, T.M. Sisk and S.A. Van Arman, Org. J. Chem., 61, 3221 (1996); https://doi.org/10.1021/jo952190f.
R.N. Sharma, K.P. Sharma and S.N. Dikshit, J. Adv. Sci. Res., 2, 5 (2011).
D.R. Richardson and P.V. Bernhardt, J. Biol. Inorg. Chem., 4, 266 (1999); https://doi.org/10.1007/s007750050312.
M.T. Tarafder, A. Kasbollah, N. Saravan, K.A. Crouse, A.M. Ali and O.K. Tin, J. Biochem. Mol. Biol. Biophys., 6, 85 (2002).
R. Sahu, D.S. Thakur and P. Kashyap, Int. J. Pharm. Sci. Nanotechnol., 5, 1757 (2002).
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M.S. Yadawe and S.A. Patil, Transition Metal Chem., 22, 220 (1997); https://doi.org/10.1023/A:1018400121316.
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H.I. Boshoff, M.B. Reed, C.E. Barry 3rd and V. Mizrahi, Cell, 113, 183 (2003); https://doi.org/10.1016/S0092-8674(03)00270-8.
I.G. Darnel and D.R. Richardson, Blood, 94, 781 (1999).
B. Murukan and K. Mohanan, J. Enzyme Inhib. Med. Chem., 22, 65 (2007); https://doi.org/10.1080/14756360601027373.
R. Rasool, S. Hasnain and N. Nishat, J. Designed Monomers Polymers, 17, 217 (2014); https://doi.org/10.1080/15685551.2013.840472.
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A. Bajpai, S. Rai and U.D.N. Bajpai, Polym. J., 29, 44 (1997); https://doi.org/10.1295/polymj.29.44.
K. Takagi, I. Tomita and T. Endo, Macromolecules, 30, 7386 (1997); https://doi.org/10.1021/ma9708959.
M.D. Hobday and T.D. Smith, Coord. Chem. Rev., 9, 83 (1973); https://doi.org/10.1016/S0010-8545(00)82081-0.
L.F. Lindoy, Q. Rev. DC Nurses Assoc., 25, 379 (1971); https://doi.org/10.1039/qr9712500379.
M. Cieslak-Golonka, A. Bartecki and S.P. Sinha, Coord. Chem. Rev., 31, 251 (1979); https://doi.org/10.1016/S0010-8545(00)80451-8.
S.C. Suh and S.C. Shim, Synth. Met., 114, 91 (2000); https://doi.org/10.1016/S0379-6779(00)00234-4.
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E.A. Bekturov and S.E. Kudaibergenov, Catalysis of Polymers, H. Huttig-Werf, p. 180 (1996).
D.W. Bruce, eds.: D.W. Bruce and D. O’Hare, Inorganic Materials, John Wiley & Sons: Chichester, p. 405 (1992).
J.P., Sauvage, Perspectives in Supramolecular Chemistry, In: Transition Metals in Supramolecular Chemistry, John Wiley & Sons: Chichester, vol. 5 (1999).
A.Y. Louie and T.J. Meade, Chem. Rev., 99, 2711 (1999); https://doi.org/10.1021/cr9804285.
R.G. Charles, Org. Synth., 39, 61 (1959); https://doi.org/10.15227/orgsyn.039.0061.
Y. Liu, H. Chao, L. Tan, Y. Yuan, W. Wei and L. Ji, J. Inorg. Biochem., 99, 530 (2005); https://doi.org/10.1016/j.jinorgbio.2004.10.030.
W.D. Charity, P.E. Ikechukwu, M.M. Fanyana, J.K. Michael and D.D. Ezekiel, Int. J. Pharm. Pharmaceut. Sci., 9, 975 (2017).
D. Nasrin, M.A. Alam, M.N. Hossain and M. Nazimuddin, Chem. J., 3, 13 (2013).
L.J. Bellamy, The Infrared Spectra of Complex Molecules, John Wiley & Sons: New York (1971).
V. Pawar, S. Joshi and V. Uma, Nigerian Soc. Exp. Biol., 23, 21 (2011).
F.A. Beckford, M.B. Niece, B.P. Lassiter, S.J. Beebe and A.A. Holder, J. Biol. Inorg. Chem., 23, 1205 (2018); https://doi.org/10.1007/s00775-018-1599-8.
S. D. Dakore, V.T. Kamble and P. Pisal, Int. J. Chem. Stud., 110, 2349 (2017).
V.K. Durg, Int. J. Pharm. Chem. Biol. Sci., 5, 77 (2015).
N.G. Yernale and M.B.H. Mathada, Bioinorg. Chem. Appl., 2014, Article ID 314963 (2014); https://doi.org/10.1155/2014/314963.
W. Hassan, R.A. Umar and M. Lawal, Breast J., 3, 18 (2006).
S. Dhar, D. Senapati, P.K. Das, P. Chattopadhyay, M. Nethaji and A.R. Chakravarty, J. Am. Chem. Soc., 125, 12118 (2003); https://doi.org/10.1021/ja036681q.