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Synthesis, Spectroscopic Investigation and Catalytic Behaviour of Histidine Substituted Nickel(II) Phthalocyanine
Corresponding Author(s) : K.R. Venugopala Reddy
Asian Journal of Chemistry,
Vol. 33 No. 10 (2021): Vol 33 Issue 10, 2021
Abstract
In this work, the oxidation behaviour of phenol and chlorophenol contaminants present in the water catalyzed by histidine substituted nickel(II) phthalocyanine (NiPc) is reported. This work comprises synthesis, characterization and study the catalytic behaviour of histidine substituted NiPc on the oxidation of phenol and their substrates like 2- and 4-chlorophenols with 4-aminoantipyrine utilizing molecular oxygen. The products from the oxidation can be analyzed by UV-Vis spectroscopy and the results confirmed the formation of superoxide anion radical were crucial for the formation of product and a feasible mechanism including a successive transfer of single electron from phenolic compounds to O2 through the axis of histidine Ni(II)Pc was reported.
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C. Guillard, J. Disdier, C. Monnet, J. Dussaud, S. Malato, J. Blanco, M.I. Maldonado and J.M. Herrmann, Appl. Catal. B, 46, 319 (2003); https://doi.org/10.1016/S0926-3373(03)00264-9
K. Abburi, J. Hazard. Mater., 105, 143 (2003); https://doi.org/10.1016/j.jhazmat.2003.08.004
X.M. Zhang and J. Wiegel, Appl. Environ. Microbiol., 56, 1119 (1990); https://doi.org/10.1128/AEM.56.4.1119-1127.1990
F.A. Banat, B. Al-Bashir, S. Al-Asheh and O. Hayajneh, Environ. Pollut., 107, 391 (2000); https://doi.org/10.1016/S0269-7491(99)00173-6
A. Sorokin, B. Meunier and J.-L. Seris, Science, 268, 1163 (1995); https://doi.org/10.1126/science.268.5214.1163
B. Meunier and A. Sorokin, Acc. Chem. Res., 30, 470 (1997); https://doi.org/10.1021/ar960275c
J. Santhanalakshmi, J. Kasthuri and N. Rajendiran, J. Mol. Catal. Chem., 265, 283 (2007); https://doi.org/10.1016/j.molcata.2006.10.012
S. Sgalla, G. Fabrizi, S. Cacchi, A. Macone, A. Bonamore and A. Boffi, J. Mol. Catal., B Enzym., 44, 144 (2007); https://doi.org/10.1016/j.molcatb.2006.10.002
M. Mifune, T. Tai, A. Iwado, H. Akizawa, J. Oda, N. Motohashi and Y. Saito, Talanta, 54, 319 (2001); https://doi.org/10.1016/S0039-9140(00)00655-X
B. Tang, G.Y. Zhang, Y. Liu and F. Han, Anal. Chim. Acta, 459, 83 (2002); https://doi.org/10.1016/S0003-2670(02)00087-9
H. Biava and S. Signorella, Polyhedron, 29, 1001 (2010); https://doi.org/10.1016/j.poly.2009.12.004
C.E. La Rotta, E. D’Elia and E.P.S. Bon, Electr. J. Biotechnol., 10, 1 (2007); https://doi.org/10.2225/vol10-issue5-fulltext-5
C.J. Clarke, W.-C. Tu, O. Levers, A. Brohl and J.P. Hallett, Chem. Rev., 118, 747 (2018); https://doi.org/10.1021/acs.chemrev.7b00571
A. Ariza, E. García-Martín, M. Salas, M.I. Montañez, C. Mayorga, N. Blanca-Lopez, I. Andreu, J. Perkins, M. Blanca, J.A.G. Agúndez and M.J. Torres, Sci. Rep., 6, 23845 (2016); https://doi.org/10.1038/srep23845
P.M. Selvakumar, E. Suresh and P.S. Subramanian, Polyhedron, 26, 749 (2007); https://doi.org/10.1016/j.poly.2006.09.004
G.T. Selvan, M. Kumaresan, R. Sivaraj, I.V.M.V. Enoch and P.M. Selvakumar, Sens. Actuators B Chem., 229, 181 (2016); https://doi.org/10.1016/j.snb.2016.01.097
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E. Emerson, J. Org. Chem., 8, 417 (1943); https://doi.org/10.1021/jo01193a004
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N. Chebotareva and T. Nyokong, Electrochim. Acta, 42, 3519 (1997); https://doi.org/10.1016/S0013-4686(97)00033-9
T. Wieprecht, J. Xia, U. Heinz, J. Dannacher and G. Schlingloff, J. Mol. Catal. Chem., 203, 113 (2003); https://doi.org/10.1016/S1381-1169(03)00406-0
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Mounesh and K.R. Venugopala Reddy, Anal. Chim. Acta, 1108, 98 (2020); https://doi.org/10.1016/j.aca.2020.02.057
M. Pari and K.R. Venugopala Reddy, Anal. Bioanal. Electrochem., 11, 1383 (2019).
M.N.K. Harish, J. Keshavayya, K.R.V. Reddy and H.R. Mallikarjuna, J. Coord. Chem., 64, 2075 (2011); https://doi.org/10.1080/00958972.2011.588705
Mounesh, K.R. Venugopala Reddy and Fasiulla, Anal. Chem. Lett., 10, 137 (2020); https://doi.org/10.1080/22297928.2020.1760132
Mounesh, P. Malathesh, N.Y. Praveen Kumara, B.S. Jilani, C.D. Mruthyunjayachari and K.R. Venugopala Reddy, Heliyon, 5, e01946 (2015); https://doi.org/10.1016/j.heliyon.2019.e01946
M. Pari and K.R. Venugopala Reddy, J. Inorg. Organomet. Polym., 30, 3511 (2020); https://doi.org/10.1007/s10904-020-01515-8
K.R. Venugopala Reddy, N.Y. Praveenkumar, T.M. Sharanakumar, Mounesh and S.K. Ganiger, Asian J. Chem., 32, 2722 (2020); https://doi.org/10.14233/ajchem.2020.22803
N.Y. Praveen Kumar, Mounesh, T M. Sharanakumar and K R. Venugopala Reddy, Chem. Pap., 75, 2683 (2021); https://doi.org/10.1007/s11696-021-01523-z
Mounesh, T.M. Sharan Kumar, N.Y. Praveen Kumar and K.R. Venugopal Reddy, Anal. Chem. Lett., 10, 620 (2020); https://doi.org/10.1080/22297928.2020.1857835
T.M. Sharanakumar, N.Y. Mounesh, N.Y.P. Kumar, K.R.V. Reddy and Suresh, Rasayan J. Chem., 13, 2133 (2020); https://doi.org/10.31788/RJC.2020.1345876
N. Rajendiran and J. Santhanalakshmi, J. Mol. Catal. Chem., 245, 185 (2006); https://doi.org/10.1016/j.molcata.2005.09.045
B. Agboola, K.I. Ozoemena and T. Nyokong, J. Mol. Catal. Chem., 227, 209 (2005); https://doi.org/10.1016/j.molcata.2004.10.041
W.J. Li, D.Z. Li, J.J. Xian, W. Chen, Y. Hu, Y. Shao and X.Z. Fu, J. Phys. Chem. C, 114, 21482 (2010); https://doi.org/10.1021/jp106659g
E.T. Saka, G. Sarki, H. Kantekin and A. Koca, Synth. Met., 214, 82 (2016); https://doi.org/10.1016/j.synthmet.2016.01.012