Thermogravimetric Analysis Of Metal Complexes Derived From 2-Phenyl-4H-Benzo[D] [3,1]-Oxazin-4-One Ligand.
DOI:
https://doi.org/10.53555/ejac.v20i2.1190Keywords:
PHBO (2-Phenyl-4H-benzo[d] [3,1]-oxazin-4-one), Metal Chelates, TGA-DTA, XRD, elemental analysis and antimicrobial activity.Abstract
Developments in the Synthesis of Certain Novel ligand PHBO (2-Phenyl-4H-benzo[d][3,1]-oxazin-4-one) is prepared from the condensation of anthranilic acid, benzoyl chloride and acetic anhydride. The heterocyclic classes which have drawn attention towards its synthesis because of their innumerable biological activities like antiviral, antitumor activity, A new complexes derived from 2-Phenyl-4H-benzo[d] [3,1]-oxazin-4-one with Ni (II), Cu (II), Cr (III), Co (III) ions. They are found to be soluble in organic solvents and characterized by IR, NMR, TGA-DTA, XRD, Elemental analysis and molar conductance measurements. The spectral data of synthesized complexes strongly support the stereochemistry of complexes and suggest the octahedral geometry for the metal ions. The thermogravimetric analysis (TGA) experiment is carried out to explore the thermal stability of the complexes. Thermal behavior of the complexes was checked in the range of temperature from 0 to 900OC in a nitrogen atmosphere. The PHBO ligand and their metal chelates have been tested for their antimicrobial activity using Broth Dilution Method and the results were discussed.
References
Emranul Kabir., Monir Uzzaman, Result in Chemistry, (4), 2022, 100606.
J. Alv´ arez-Builla, J. Barluenga, Mod. Heterocycl. Chem. 1 (2011) 1–9.
D. Barton, W.D. Ollis, Compr. Org. Chem. (1979) 357.
R. Mahdi Ubaid Mahmood, N. Mahmood Aljamali, 7 (2020) 2020.
Y. Ogawa, E. Tokunaga, O. Kobayashi, K. Hirai, N. Shibata, IScience 23 (2020),101467.
Adejoke D. Osinubi., Josephat U. Izunobi, Research Gate, CT, 2021.
Sakiyan I., Logoglu E., Arslan S., Sari N. and Sakiyan N., Biometals, 2004, 17, 115.
Pandeya S.N., Sriram D., Nath G. and DeCleeq E., European J. Pharm., 1999, 9, 25.
Chen H. and Rhodes J., J. Mol. Med., 1996, 74, 497.
Molla B.S., Rao B.S., Shridhara K. and Akberali P.M., Farmaco, 2000, 55, 338.
Islam M.R., Mirza A.H., Huda Q.M.N. and Khan B.R., J. Bang. Chem. Soc., 1989,2,87.
Ali M.M., Jesmin M., Sarkar M.K., Salahuddin M.S., Habib M.R. and Khanam J.A., Int. J. Biol. Chem. Sci., 2008, 2, 292.
K. Mészáros Szécsényi, V. M. Leovac., K. Jaæimoviæ et.al., Journal of Thermal Analysis and Calorimetry, Vol. 63 (2001), p.723–732.
Gamze Koz, Hale Kaya, Demet Astley, Ishan Yasa, Stephen T. Astley; Guj. Sci., 24(3), 2011, p.407.
Abu Shama, Oriental Journal of Chemistry, 26 (4), 2010, p. 1497.
Mahmoud M. Mashaly., Zinab H. Abd-Elwahab and Abeer A. Faheim., Journal of Chinese Chem. Soc., 51, 2004, p. 901.
Tadewos Damena., MamaruBitewAlem., Digafie Zeleke., Frontiers in Chemistry, Nov-2022.
H.M.F. Madkour., ARKIVOC, 2004 (i), 36-54.
H. Annita Zhong., Jay A. Labinger., and John E. Bercaw, J. AM. CHEM. SOC. 9, VOL. 124, NO. 7, 2002, p. 1399.
ALI HAMMADI SAMIR., Oriental Journal of Chemistry, Vol.33, No. (3), 2017, p. 1422-1432.
Bipransh Kumar Tiwary., Ravindra Kailasrao Zirmire., Kiran Pradhan., Ashis Kumar Nanda., international journal of Pharmacy and Pharmaceutical Sciences, Vol 6, Issue 3, 2014. P. 176-179.
Suraj B. Ade., M.N. Deshpande and J.H. Deshmukh, Rasayan. J. Chem, Vol. 5, No.1 2012, p. 10-15.
Shobhana Sharma., Poonam Yadav., Seema., and Suman Kumari, Rasayan. J. Chem, Vol. 15, No.2 2022, p. 836-841.
C, Gh, Macarovici analiza., Chimica. Cantitativa Anorganica, Inorganic Quantitative Chemical Analysis, Editura, Academiei, R.S.R. Bucuresti, 1979, p. 364.
SURAJ B. ADE., D.G. KOLHATKAR., AND M.N. DESHPANDE, International Journal of Pharma and Bio Sciences, Vol 3, Issue 2, 2012.
Samar A. Aly., Safaa S. Hassan., HanaaA.El-Boraey., Ayman Eldourghamy., Ehab M. Abdalla., et.al, Arabian Journal for Science and Engineering, 49: 2024, p.361–379.
Pingalkar S.R. and Deshpande M.N., Orient. J. Chem., 23(1), 2007, p. 265.
Chandra Sekhara Rao G M et al, Int Jou Phar Chem 4(2), 2023, p. 7-11.
Dixit, B. C. and Patel, H.M.., E-Journal of Chemistry, 8(2), 2011, p. 615.
Mapari, A.K. and Mangaokar, K.V.., International Journal Chem. Tech, Res., Vol, 3(2), 2011, p. 636.
Md. Kudrat-E-Zahan., Md. Masuqul Haque., Lokonuzzaman Ahmmed., M. Sher Ali., International Journal of Materials Science and Applications, 4(2), 2015, p. 120-123.
Chioma Festus., International Journal of Chemistry, Pharmacy & Technology, Vol. 2, No.5, 2017, p. 202-211.
Thakur, G.A. and Shaikh, M.M., Acta Poloniae Pharmaceutical Drug Res., Vol. 63(2), 2006, p.95.
Ebd EI Wahed, M.G., Thermo. Chimica Acta., Vol 182 (2), 1991, p. 181.
Thakor, Y, J., Patel S.G and Patel, K. N., Der Chimica Sinica., vol 2(1), 2011, p. 43.
D. A. Köse and H. Necefo lu., Journal of Thermal Analysis and Calorimetry, Vol. 93(2), 2008, p. 509-514.
Saleh A. Ahmed., J. of university of Anbar for pure science, Vol.4, 2010, p.1.
El-Tabi., A.S., Shakofa., M.M.E., El-SZeidy., A.M.A. and Al-Hakimi A.N., J. Korean Chem. Soc., Vol. 55(1).
Modi, C.K., Patel A. S, and Thaker, B, T., E- Journal of Chemistry, Vol.2 (6), 2005, p.21.
Adesoji A. Olanrewaj, Collins U. Ibeji, Festus S. Fabiyi., Indian Journal of Heterocyclic Chemistry, Vol. 28. (03), 2018, p. 351-361.
V. Mukil Meenakshi, S. Balasubramaniyan, R. Govindharaju and M. Marlin Risana., Indian Journal of Natural Sciences, Vol.13, Issue 71, 2022.
Ghosh, S., and Malik, S., E-Journal of Chemistry,7(4), 2010, p.1391.
Baluja, S., Solanki, A., and Kachhadia, N., Journal of the Iranian Chemical Society, Vol. 3(4), 2006, p. 312.
Pingalkar S.R. and Deshpande M.N., Orient. J. Chem., 23(1), 2007, p. 265.
Mohammed H. A. Al-Amery, Journal of Al-Nahrain University, Vol.15 (3),2012, p.55-61.
SURAJ B. ADE., D.G. KOLHATKAR AND M.N. DESHPANDE, International Journal of Pharma and Bio Sciences, Vol 3, Issue 2, 2012.
Suraj B. Ade., M.N. Deshpande and J.H. Deshmukh, Rasayan Journal of Chemistry, Vol. 5, No.1, 2012, p. 10-15.
Tabot, P.C., and Mackinnon, I.D.R., Journal of Material Science Letter, Vol. 13 (18), 1994, p. 1377.
Clinical microbiology procedure handbook, vol.2, chapter 5 page no 5.0.1 Henry d. Isenberg, 2nd edition, National Committee for Clinical Laboratory Standards, Methods for Dilution, Antimicrobial Susceptibility Tests for Bacteria, that Grow Aerobically Approved Standard, (M7A5), 9th ed.; National, Committee for Clinical Laboratory Standards: Wayne, PA, 2010.
Shadowy, S. In Manual of Clinical Microbiology; Albert., Ed.; ASM Press: Washington, DC, 1991; p 1173.
Rattan, A. Antimicrobials in Laboratory Medicine; BI, Churchill Livingstone: India, 2000; p 85.