This work is licensed under a Creative Commons Attribution 4.0 International License.
Gas Chromatographic Technique Employed for Catalytic Investigation of Novel Phthalocyanines
Corresponding Author(s) : C.R. Ravikumar
Asian Journal of Chemistry,
Vol. 35 No. 7 (2023): Vol 35 Issue 7 (2023)
Abstract
The primaquine substituted Fe(II) phthalocyanine (PQFePc) and Co(II) phthalocyanine (PQCoPc) catalysts were prepared by using amide linkage method. The physical and chemical properties have been investigated by FTIR, mass, UV-Vis, TGA, XRD and elemental analysis. The catalytic oxidation of benzyl alcohol was determined by PQFePc and PQCoPc complexes by varying parameters like temperature, oxidant/catalytic ratio and substance/catalyst ratio. The optimization of catalytic oxidation reaction has been effectively achieved for the determination of benzyl alcohol (Bzalc) to benzaldehyde (Bzald). The PQCoPc and PQFePc exhibited excellent catalytic behaviour for the oxidation of benzyl alcohol obtaining high yield and good selectivity.
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- Mounesh, K.R. Venugopal Reddy and Fasiulla, Anal. Chem. Lett., 10, 137 (2020); https://doi.org/10.1080/22297928.2020.1760132
- Mounesh, P. Malathesh, N.Y. Praveen Kumara, C.D. Mruthyunjayachari, B.S. Jilani and K.R. Venugopala Reddy, Heliyon, 5, e01946 (2019); https://doi.org/10.1016/j.heliyon.2019.e01946
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- Q.G. Ren, S.Y. Chen, X.T. Zhou and H.B. Ji, Bioorg. Med. Chem., 18, 8144 (2010); https://doi.org/10.1016/j.bmc.2010.10.026
- R. Rahimi, E. Gholamrezapor and M.R. Naimi-jamal, Inorg. Chem. Commun., 14, 1561 (2011); https://doi.org/10.1016/j.inoche.2011.05.056
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I. Acar, S. Topçu, Z. Biyiklioglu and H. Kantekin, Color. Technol., 259, 4 (2013); https://doi.org/10.1111/cote.12031
T.M. Sharanakumar, 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
B. Sanna Jilani, C.D. Mruthyunjayachari, P. Malathesh, Mounesh, T.M. Sharankumar and K.R.V. Reddy, Sens. Actuators B Chem., 301, 127078 (2019); https://doi.org/10.1016/j.snb.2019.127078
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P.K. Mounesh, N.Y. Praveenkumar, T.M. Sharankumar and K.R. Venugopal Reddy, Electrochem. Sci. Adv., 2, e2100006 (2021); https://doi.org/10.1002/elsa.202100006
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T. Inabe and K. Morimoto, Synth. Met., 86, 1799 (1997); https://doi.org/10.1016/S0379-6779(97)80909-5
A.S. Komolov and P.J. Moller, Synth. Met., 138, 119 (2003); https://doi.org/10.1016/S0379-6779(02)01286-9
X. Zhang, J. Song, C. Zhou, L. Zhou and M. Gong, J. Lumin., 149, 69 (2014); https://doi.org/10.1016/j.jlumin.2014.01.012
A. Kumar, J. Brunet, C. Varenne, A. Ndiaye, A. Pauly, M. Penza and M. Alvisi, Sens. Actuators B Chem., 210, 398 (2015); https://doi.org/10.1016/j.snb.2015.01.010
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O.M. Bankole, J. Britton and T. Nyokong, Polyhedron, 88, 73 (2015); https://doi.org/10.1016/j.poly.2014.12.020
D. Çakir, C. Göl, V. Çakir, M. Durmus, Z. Biyiklioglu and H. Kantekin, J. Lumin., 159, 79 (2015); https://doi.org/10.1016/j.jlumin.2014.10.044
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M.P. Chaudhari and S.B. Sawant, Chem. Eng. J., 106, 111 (2005); https://doi.org/10.1016/j.cej.2004.07.014
S. Tsuruya, H. Miyamoto, T. Sakae and M. Masai, J. Catal., 64, 260 (1980); https://doi.org/10.1016/0021-9517(80)90501-1
R.A. Sheldon and J.K. Kochi, Metal-Catalyzed Oxidation of Organic Compounds, Academic: New York (1981).
M. Hudlicky, Oxidations in Organic Chemistry, ACS Monograph Series 186, American Chemical Society, Washington, p. 174 (1990).
A. Aktas, I. Acar, E.T. Saka, Z. Biyiklioglu and H. Kantekin, J. Incl. Phenom. Macrocycl. Chem., 86, 183 (2016); https://doi.org/10.1007/s10847-016-0650-z
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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
Mounesh, K.R. Venugopal Reddy and Fasiulla, Anal. Chem. Lett., 10, 137 (2020); https://doi.org/10.1080/22297928.2020.1760132
Mounesh, P. Malathesh, N.Y. Praveen Kumara, C.D. Mruthyunjayachari, B.S. Jilani and K.R. Venugopala Reddy, Heliyon, 5, e01946 (2019); https://doi.org/10.1016/j.heliyon.2019.e01946
M. Grossman, G. Glosser, J. Kalmanson, J. Morris, M.B. Stern and H.I. Hurtig, J. Neurol. Sci., 184, 123 (2001); https://doi.org/10.1016/S0022-510X(00)00491-3
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V. Çakir, E.T. Saka, Z. Biyiklioglu and H. Kantekin, Synth. Met., 197, 233 (2014); https://doi.org/10.1016/j.synthmet.2014.09.022
S.R. Ali, V.K. Bansal, A.A. Khan, S.K. Jain and M.A. Ansari, J. Mol. Catal. Chem., 303, 60 (2009); https://doi.org/10.1016/j.molcata.2008.12.020
A. Rezaeifard, M. Jafarpour and A. Naeimi, Catal. Commun., 16, 240 (2011); https://doi.org/10.1016/j.catcom.2011.09.039
M. Ozer, F. Yilmaz, H. Erer, I. Kani and O. Bekaroglu, Appl. Organomet. Chem., 23, 55 (2009); https://doi.org/10.1002/aoc.1471
Q.G. Ren, S.Y. Chen, X.T. Zhou and H.B. Ji, Bioorg. Med. Chem., 18, 8144 (2010); https://doi.org/10.1016/j.bmc.2010.10.026
R. Rahimi, E. Gholamrezapor and M.R. Naimi-jamal, Inorg. Chem. Commun., 14, 1561 (2011); https://doi.org/10.1016/j.inoche.2011.05.056
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