Copyright (c) 2020 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis, Structure and Antioxidant Activity of Mixed Ruthenium(III) Benzoyl Pyridine Complex
Corresponding Author(s) : E. Jayanthi
Asian Journal of Chemistry,
Vol. 32 No. 3 (2020): Vol 32 Issue 3
Abstract
A new ruthenium arsine complex was prepared by reacting equimolar ratio of [RuBr3(AsPh3)3] and 2-benzoyl pyridine. It was characterized by microanalysis, FT-IR and single crystal X-ray diffraction studies. X-ray diffraction data showed the distorted octahedral geometry of the complex. The pyridine nitrogen and carbonyl oxygen of the ligand coordinated with the metal center. Antioxidant activity of the complex was analyzed using different assays, which manifested significant activity. It has been found that a newly synthesized complex possessed better antioxidant activity than the ligand and precursor complex.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- R. Dua, S. Shrivastava, S.K. Sonwane and S.K. Srivastava, Adv. Biol. Res. (Faisalabad), 5, 120 (2011).
- L. Mercs and M. Albrecht, Chem. Soc. Rev., 39, 1903 (2010); https://doi.org/10.1039/b902238b
- C. Kaes, A. Katz and M.W. Hosseini, Chem. Rev., 100, 3553 (2000); https://doi.org/10.1021/cr990376z
- F.W. Bergstrom, Chem. Rev., 35, 77 (1944); https://doi.org/10.1021/cr60111a001
- P. Sathyadevi, P. Krishnamoorthy, E. Jayanthi, R.R. Butorac, A.H. Cowley and N. Dharmaraj, Inorg. Chim. Acta, 384, 83 (2012); https://doi.org/10.1016/j.ica.2011.11.033
- T.K. Köprülü, S. Ökten, S. Tekin and O. Çakmak, J. Biochem. Mol. Toxicol., 33, e22260 (2019); https://doi.org/10.1002/jbt.22260
- S. Li, H. Zhang and J. Liu, Trans. Nonferr. Met. Soc. China, 17, 318 (2007); https://doi.org/10.1016/S1003-6326(07)60092-2
- M.N. Hopkinson, C. Richter, M. Schedler and F. Glorius, Nature, 510, 485 (2014); https://doi.org/10.1038/nature13384
- S. Singh, N. Bharti and P.P. Mohapatra, Chem. Rev., 109, 1900 (2009); https://doi.org/10.1021/cr068217k
- F.A.K. Khan, Z. Zaheer, J.N. Sangshetti, R.H. Patil and M. Farooqui, Bioorg. Med. Chem. Lett., 27, 567 (2017); https://doi.org/10.1016/j.bmcl.2016.12.018
- N.T. Huy, D.T. Uyen, A. Maeda, D.T.X. Trang, T. Oida, S. Harada and K. Kamei, Antimicrob. Agents Chemother., 51, 350 (2007); https://doi.org/10.1128/AAC.00985-06
- M. Gras, B. Therrien, G. Suss-Fink, A. Casini, F. Edafe and P.J. Dyson, J. Organomet. Chem., 695, 1119 (2010); https://doi.org/10.1016/j.jorganchem.2010.01.020
- M.S.A. Gill, S.S. Hassan and N. Ahemad, Eur. J. Med. Chem., 179, 423 (2019); https://doi.org/10.1016/j.ejmech.2019.06.058
- M.A. Fakhfakh, A. Fournet, E. Prina, J.-F. Mouscadet, X. Franck, R. Hocquemiller and B. Figadère, Bioorg. Med. Chem., 11, 5013 (2003); https://doi.org/10.1016/j.bmc.2003.09.007
- A. Bari, D. Grenier, J. Azelmat, S.A. Syed, A.M. AlObaid and E.C. Hosten, Chem. Biol. Drug Des., 94, 1750 (2019); https://doi.org/10.1111/cbdd.13576
- C.X. Zhang and S.J. Lippard, Curr. Opin. Chem. Biol., 7, 481 (2003); https://doi.org/10.1016/S1367-5931(03)00081-4
- S.K. Bharti and S.K. Singh, Pharm. Lett., 1, 39 (2009).
- A.A. Raj, R. Raghunathan , M.R. SrideviKumari and N. Raman, Bioorg. Med. Chem., 11, 407 (2003); https://doi.org/10.1016/S0968-0896(02)00439-X
- F. Li, M. Feterl, Y. Mulyana, J.M. Warner, J.G. Collins and F.R. Keene, J. Antimicrob. Chemother., 67, 2686 (2012); https://doi.org/10.1093/jac/dks291
- D. Gambino and L. Otero, Inorg. Chim. Acta, 393, 103 (2012); https://doi.org/10.1016/j.ica.2012.05.028
- X.L. Hong, H. Li and C.H. Peng, J. Mol. Struct., 990, 197 (2011); https://doi.org/10.1016/j.molstruc.2011.01.045
- J.M. da Silveira Carvalho, A.H. de Morais Batista, N.A.P. Nogueira, A.K.M. Holanda, J.R. de Sousa, D. Zampieri, M.J.B. Bezerra, F. Stefânio Barreto, M.O. de Moraes, A.A. Batista, A.C.S. Gondim, T. de F. Paulo, L.G. de França Lopes and E.H.S. Sousa, New J. Chem., 41, 13085 (2017); https://doi.org/10.1039/C7NJ02943H
- E. Jayanthi, M. Anusuya, N.S.P. Bhuvanesh, K.A. Khalil and N. Dharmaraj, J. Coord. Chem., 68, 3551 (2015); https://doi.org/10.1080/00958972.2015.1077950
- S.S. Valvassori, M.P. Cristiano, D.C. Cardoso, G.D. Santos, M.R. Martins, J. Quevedo and M.M.S. da Paula, Neurochem. Res., 31, 1457 (2006); https://doi.org/10.1007/s11064-006-9198-4
- E. Jayanthi, S. Kalaiselvi, V.V. Padma, N.S.P. Bhuvanesh and N. Dharmaraj, Dalton Trans., 45, 1693 (2016); https://doi.org/10.1039/C5DT03849A
- R. Prabhakaran, V. Krishnan, K. Pasumpon, D. Sukanya, E. Wendel, C. Jayabalakrishnan, H. Bertagnolli and K. Natarajan, Appl. Organomet. Chem., 20, 203 (2006); https://doi.org/10.1002/aoc.1026
- F.E. Poynton, S.A. Bright, S. Blasco, D.C. Williams, J.M. Kelly and T. Gunnlaugsson, Chem. Soc. Rev., 46, 7706 (2017); https://doi.org/10.1039/C7CS00680B
- T.S. Kamatchi, N. Chitrapriya, S.K. Kim, F.R. Fronczek and K. Natarajan, Eur. J. Med. Chem., 59, 253 (2013); https://doi.org/10.1016/j.ejmech.2012.11.024
- K. Natarajan, R.K. Poddar and U. Agarwala, J. Inorg. Nucl. Chem., 39, 431 (1977); https://doi.org/10.1016/0022-1902(77)80056-0
- O.V. Dolomanov, L.J. Bourhis, R.J. Gildea, J.A.K. Howard and H. Puschmann, J. Appl. Cryst., 42, 339 (2009); https://doi.org/10.1107/S0021889808042726
- SADABS, Program for Absorption Correction of Area Detector Frames; Bruker AXS Inc., 5465 East Cheryl Parkway, Madison, USA.
- K. Mishra, K. Ojha and N.K. Chaudhury, Food Chem., 130, 1036 (2012); https://doi.org/10.1016/j.foodchem.2011.07.127
- R. Manian, N. Anusuya, P. Siddhuraju and S. Manian, Food Chem., 107, 1000 (2008); https://doi.org/10.1016/j.foodchem.2007.09.008
- T. Krishnaswamy, P. Subramaniam, M. Sellamuthu and K. Krishnamoorthy, Int. J. Green Pharm., 8, 58 (2014); https://doi.org/10.4103/0973-8258.126826
- C. Beauchamp and I. Fridovich, Anal. Biochem., 44, 276 (1971); https://doi.org/10.1016/0003-2697(71)90370-8
References
R. Dua, S. Shrivastava, S.K. Sonwane and S.K. Srivastava, Adv. Biol. Res. (Faisalabad), 5, 120 (2011).
L. Mercs and M. Albrecht, Chem. Soc. Rev., 39, 1903 (2010); https://doi.org/10.1039/b902238b
C. Kaes, A. Katz and M.W. Hosseini, Chem. Rev., 100, 3553 (2000); https://doi.org/10.1021/cr990376z
F.W. Bergstrom, Chem. Rev., 35, 77 (1944); https://doi.org/10.1021/cr60111a001
P. Sathyadevi, P. Krishnamoorthy, E. Jayanthi, R.R. Butorac, A.H. Cowley and N. Dharmaraj, Inorg. Chim. Acta, 384, 83 (2012); https://doi.org/10.1016/j.ica.2011.11.033
T.K. Köprülü, S. Ökten, S. Tekin and O. Çakmak, J. Biochem. Mol. Toxicol., 33, e22260 (2019); https://doi.org/10.1002/jbt.22260
S. Li, H. Zhang and J. Liu, Trans. Nonferr. Met. Soc. China, 17, 318 (2007); https://doi.org/10.1016/S1003-6326(07)60092-2
M.N. Hopkinson, C. Richter, M. Schedler and F. Glorius, Nature, 510, 485 (2014); https://doi.org/10.1038/nature13384
S. Singh, N. Bharti and P.P. Mohapatra, Chem. Rev., 109, 1900 (2009); https://doi.org/10.1021/cr068217k
F.A.K. Khan, Z. Zaheer, J.N. Sangshetti, R.H. Patil and M. Farooqui, Bioorg. Med. Chem. Lett., 27, 567 (2017); https://doi.org/10.1016/j.bmcl.2016.12.018
N.T. Huy, D.T. Uyen, A. Maeda, D.T.X. Trang, T. Oida, S. Harada and K. Kamei, Antimicrob. Agents Chemother., 51, 350 (2007); https://doi.org/10.1128/AAC.00985-06
M. Gras, B. Therrien, G. Suss-Fink, A. Casini, F. Edafe and P.J. Dyson, J. Organomet. Chem., 695, 1119 (2010); https://doi.org/10.1016/j.jorganchem.2010.01.020
M.S.A. Gill, S.S. Hassan and N. Ahemad, Eur. J. Med. Chem., 179, 423 (2019); https://doi.org/10.1016/j.ejmech.2019.06.058
M.A. Fakhfakh, A. Fournet, E. Prina, J.-F. Mouscadet, X. Franck, R. Hocquemiller and B. Figadère, Bioorg. Med. Chem., 11, 5013 (2003); https://doi.org/10.1016/j.bmc.2003.09.007
A. Bari, D. Grenier, J. Azelmat, S.A. Syed, A.M. AlObaid and E.C. Hosten, Chem. Biol. Drug Des., 94, 1750 (2019); https://doi.org/10.1111/cbdd.13576
C.X. Zhang and S.J. Lippard, Curr. Opin. Chem. Biol., 7, 481 (2003); https://doi.org/10.1016/S1367-5931(03)00081-4
S.K. Bharti and S.K. Singh, Pharm. Lett., 1, 39 (2009).
A.A. Raj, R. Raghunathan , M.R. SrideviKumari and N. Raman, Bioorg. Med. Chem., 11, 407 (2003); https://doi.org/10.1016/S0968-0896(02)00439-X
F. Li, M. Feterl, Y. Mulyana, J.M. Warner, J.G. Collins and F.R. Keene, J. Antimicrob. Chemother., 67, 2686 (2012); https://doi.org/10.1093/jac/dks291
D. Gambino and L. Otero, Inorg. Chim. Acta, 393, 103 (2012); https://doi.org/10.1016/j.ica.2012.05.028
X.L. Hong, H. Li and C.H. Peng, J. Mol. Struct., 990, 197 (2011); https://doi.org/10.1016/j.molstruc.2011.01.045
J.M. da Silveira Carvalho, A.H. de Morais Batista, N.A.P. Nogueira, A.K.M. Holanda, J.R. de Sousa, D. Zampieri, M.J.B. Bezerra, F. Stefânio Barreto, M.O. de Moraes, A.A. Batista, A.C.S. Gondim, T. de F. Paulo, L.G. de França Lopes and E.H.S. Sousa, New J. Chem., 41, 13085 (2017); https://doi.org/10.1039/C7NJ02943H
E. Jayanthi, M. Anusuya, N.S.P. Bhuvanesh, K.A. Khalil and N. Dharmaraj, J. Coord. Chem., 68, 3551 (2015); https://doi.org/10.1080/00958972.2015.1077950
S.S. Valvassori, M.P. Cristiano, D.C. Cardoso, G.D. Santos, M.R. Martins, J. Quevedo and M.M.S. da Paula, Neurochem. Res., 31, 1457 (2006); https://doi.org/10.1007/s11064-006-9198-4
E. Jayanthi, S. Kalaiselvi, V.V. Padma, N.S.P. Bhuvanesh and N. Dharmaraj, Dalton Trans., 45, 1693 (2016); https://doi.org/10.1039/C5DT03849A
R. Prabhakaran, V. Krishnan, K. Pasumpon, D. Sukanya, E. Wendel, C. Jayabalakrishnan, H. Bertagnolli and K. Natarajan, Appl. Organomet. Chem., 20, 203 (2006); https://doi.org/10.1002/aoc.1026
F.E. Poynton, S.A. Bright, S. Blasco, D.C. Williams, J.M. Kelly and T. Gunnlaugsson, Chem. Soc. Rev., 46, 7706 (2017); https://doi.org/10.1039/C7CS00680B
T.S. Kamatchi, N. Chitrapriya, S.K. Kim, F.R. Fronczek and K. Natarajan, Eur. J. Med. Chem., 59, 253 (2013); https://doi.org/10.1016/j.ejmech.2012.11.024
K. Natarajan, R.K. Poddar and U. Agarwala, J. Inorg. Nucl. Chem., 39, 431 (1977); https://doi.org/10.1016/0022-1902(77)80056-0
O.V. Dolomanov, L.J. Bourhis, R.J. Gildea, J.A.K. Howard and H. Puschmann, J. Appl. Cryst., 42, 339 (2009); https://doi.org/10.1107/S0021889808042726
SADABS, Program for Absorption Correction of Area Detector Frames; Bruker AXS Inc., 5465 East Cheryl Parkway, Madison, USA.
K. Mishra, K. Ojha and N.K. Chaudhury, Food Chem., 130, 1036 (2012); https://doi.org/10.1016/j.foodchem.2011.07.127
R. Manian, N. Anusuya, P. Siddhuraju and S. Manian, Food Chem., 107, 1000 (2008); https://doi.org/10.1016/j.foodchem.2007.09.008
T. Krishnaswamy, P. Subramaniam, M. Sellamuthu and K. Krishnamoorthy, Int. J. Green Pharm., 8, 58 (2014); https://doi.org/10.4103/0973-8258.126826
C. Beauchamp and I. Fridovich, Anal. Biochem., 44, 276 (1971); https://doi.org/10.1016/0003-2697(71)90370-8