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Vol. 34 No. 8 (2022): Vol 34 Issue 8, 2022

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Organyltellurium(IV) Bidentate Schiff Base Metal Complexes: Synthesis, Characterization and Biological Activities

https://doi.org/10.14233/ajchem.2022.23679
Nidhi Antil
Department of Chemistry, Maharshi Dayanand University, Rohtak-124001, India
Mahak Dalal
Department of Chemistry, Maharshi Dayanand University, Rohtak-124001, India
K.K. Verma
Department of Chemistry, Maharshi Dayanand University, Rohtak-124001, India
Sapana Garg
Department of Chemistry, Maharshi Dayanand University, Rohtak-124001, India

Corresponding Author(s) : Sapana Garg

sapanagarg1511@gmail.com

Asian Journal of Chemistry, Vol. 34 No. 8 (2022): Vol 34 Issue 8, 2022

Abstract

Condensation of 5-(hydroxymethyl)furan-2-carboxaldehyde with 4-toluidine yielded a Schiff base (5-((p-tolylimino)methyl)furan-2-ol). A series of seven novel hexa-coordinated organyltellurium(IV) complexes of type TeCl4·HMeFPT, RTeCl3·HMeFPT and R2TeCl2·HMeFPT (where R belongs to 4-methoxyphenyl, 4-hydroxyphenyl and 3-methyl-4-hydroxyphenyl; L belongs to HMeFPT i.e. Schiff base have been prepared and characterized by molar conductance, IR, UV, 1H NMR, 13C NMR, mass spectroscopy and elemental analysis. Thus according to spectroscopic studies, Schiff base ligand functions as a NO donor bidentate ligand across all organyltellurium(IV) complexes via the azomethine nitrogen atom and the oxygen atom of the furan ring. The above mentioned spectroscopic analysis indicated that all the organyltellurium(IV) complexes have distorted octahedral geometry. Schiff base and all the organyltellurium(IV) complexes had their geometry optimized and theoretical quantum mechanical characteristics computed. The octahedral geometry for complexes is also suggested by this computing analysis. The antimicrobial property of the Schiff base ligand and its organyltellurium(IV) complexes was evaluated in vitro against different bacterial strains viz. A. clavatus, C. albicans, A. niger, S. pyogenes, S. aureus, E. coli and P. aerugenosa. Antimicrobial property of heterocyclic bidentate Schiff base and its organyltellurium(IV) complexes was found to be significantly greater than that of some standard antibiotics.

Keywords

5-(Hydroxymethyl)furan-2-carboxaldehyde 4-Toluidine Organyltellurium Antimicrobial activity
Antil, N., Dalal, M., Verma, K., & Garg, S. (2022). Organyltellurium(IV) Bidentate Schiff Base Metal Complexes: Synthesis, Characterization and Biological Activities. Asian Journal of Chemistry, 34(8), 2008–2016. https://doi.org/10.14233/ajchem.2022.23679
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References
  1. A.M. Abu-Dief and I.M.A. Mohamed, Beni. Suef Univ. J. Basic Appl. Sci., 4, 119 (2015); https://doi.org/10.1016/j.bjbas.2015.05.004
  2. H.-Q. Chang, L. Jia, J. Xu, T.-F. Zhu, Z.-Q. Xu, R.-H. Chen, T.-L. Ma, Y. Wang and W.-N. Wu, J. Mol. Struct., 1106, 366 (2016); https://doi.org/10.1016/j.molstruc.2015.11.001
  3. E. Raczuk, B. Dmochowska, J. Samaszko-Fiertek and J. Madaj, Molecules, 27, 787 (2022); https://doi.org/10.3390/molecules27030787
  4. S. Kumar, D.N. Dhar and P. Saxena, J. Sci. Ind. Res. (India), 68, 181 (2009).
  5. R. Savalia, A. Patel, P. Tivedi, H. Gohel and D. Khetani, J. Chem. Sci., 2231, 606X (2013).
  6. G. Grivani, G. Bruno, H.A. Rudbari, A.D. Khalaji and P. Pourteimouri, Inorg. Chem. Commun., 18, 15 (2012); https://doi.org/10.1016/j.inoche.2011.12.044
  7. K.C. Gupta and A.K. Sutar, Coord. Chem. Rev., 252, 1420 (2008); https://doi.org/10.1016/j.ccr.2007.09.005
  8. S. Banerjee, C. Adhikary, C. Rizzoli and R. Pal, Inorg. Chim. Acta, 409, 202 (2014); https://doi.org/10.1016/j.ica.2013.09.032
  9. X. Yun, X. Hu, Z. Jin, J. Hu, C. Yan, J. Yao and H. Li, J. Mol. Catal. Chem., 327, 25 (2010); https://doi.org/10.1016/j.molcata.2010.05.006
  10. G. Grivani, A. Ghavami, M. Kuèeráková, M. Dušek and A.D. Khalaji, J. Mol. Struct., 1076, 326 (2014); https://doi.org/10.1016/j.molstruc.2014.07.073
  11. P. Fita, E. Luzina, T. Dziembowska, C. Radzewicz and A. Grabowska, J. Chem. Phys., 125, 184508 (2006); https://doi.org/10.1063/1.2371058
  12. T. Wei, G. Gao, W. Qu, B. Shi, Q. Lin, H. Yao and Y. Zhang, Sens. Actuators B Chem., 199, 142 (2014); https://doi.org/10.1016/j.snb.2014.03.084
  13. G. Grivani, V. Tahmasebi, K. Eskandari, A.D. Khalaji, G. Bruno and H.A. Rudbari, J. Mol. Struct., 1054-1055, 100 (2013); https://doi.org/10.1016/j.molstruc.2013.09.026
  14. M. Ghassemzadeh, R. Firouzi, S. Shirkhani, S. Amiri and B. Neumüller, Polyhedron, 69, 188 (2014); https://doi.org/10.1016/j.poly.2013.11.030
  15. L.E.H. Paul, I.C. Foehn, A. Schwarzer, E. Brendler and U. Böhme, Inorg. Chim. Acta, 423, 268 (2014); https://doi.org/10.1016/j.ica.2014.08.026
  16. K.S. Kumar, S. Ganguly, R. Veerasamy and E. De Clercq, Eur. J. Med. Chem., 45, 5474 (2010); https://doi.org/10.1016/j.ejmech.2010.07.058
  17. C.M. da Silva, D.L. da Silva, L.V. Modolo, R.B. Alves, M.A. de Resende, C.V.B. Martins and Â. de Fátima, J. Adv. Res., 2, 1 (2011); https://doi.org/10.1016/j.jare.2010.05.004
  18. S. Amer, N. El-Wakiel and H. El-Ghamry, J. Mol. Struct., 1049, 326 (2013); https://doi.org/10.1016/j.molstruc.2013.06.059
  19. S.M. Bensaber, H. Allafe, N.B. Ermeli, S.B. Mohamed, A. Zetrini, S.G. Alsabri, M. Erhuma, A. Hermann, M.I. Jaeda and A.M. Gbaj, Med. Chem., 23, 5120 (2014); https://doi.org/10.1007/s00044-014-1064-3
  20. A. Sinha, K. Banerjee, A. Banerjee, S. Das and S.K. Choudhuri, J. Organomet. Chem., 34, 772 (2014); https://doi.org/10.1016/j.jorganchem.2014.08.032
  21. S. Shahidi, M. Ghoranneviss, B. Moazzenchi, A. Rashidi and M. Mirjalili, Plasma Process. Polym., 4(S1), S1098 (2007); https://doi.org/10.1002/ppap.200732412
  22. M. Hasanzadeh, M. Salehi, M. Kubicki, S.M. Shahcheragh, M. Pyziak, G. Dutkiewicz and A. Khaleghian, Transition Met. Chem., 39, 623 (2014); https://doi.org/10.1007/s11243-014-9841-x
  23. S. Chandra and A. Kumar, Spectrochim. Acta A Mol. Biomol. Spectrosc., 66, 1347 (2007); https://doi.org/10.1016/j.saa.2006.04.047
  24. S. Sharma, F. Athar, M.R. Maurya, F. Naqvi and A. Azam, Eur. J. Med. Chem., 40, 557 (2005); https://doi.org/10.1016/j.ejmech.2005.01.003
  25. N.S. Youssef and K.H. Hegab, Synth. React Met. Org. Nano-Met. Chem., 35, 391 (2005); https://doi.org/10.1081/SIM-200059215
  26. M. Kumar, K.K. Verma and S. Garg, Asian J. Chem., 33, 1236 (2021); https://doi.org/10.14233/ajchem.2021.23159
  27. M. Kumar, P.J. Darolia, N. Antil, M. Dalal, J. Narwal, K.K. Verma and S. Garg, Asian J. Chem., 33, 1749 (2021); https://doi.org/10.14233/ajchem.2021.23214
  28. S. Deepak Chouhan, K.K. Verma and S. Garg, Int. J. Chem. Sci., 15, 182 (2017).
  29. Ö. Güngör and P. Gürkan, J. Mol. Struct., 1074, 62 (2014); https://doi.org/10.1016/j.molstruc.2014.05.032
  30. A.K. Singh, S.K. Pandey, O.P. Pandey and S.K. Sengupta, J. Mol. Struct., 1074, 376 (2014); https://doi.org/10.1016/j.molstruc.2014.06.009
  31. H.A.R. Pramanik, D. Das, P.C. Paul, P. Mondal and C.R. Bhattacharjee, J. Mol. Struct., 1059, 309 (2014); https://doi.org/10.1016/j.molstruc.2013.12.009
  32. N.N. Greenwood, B. Straughan and A.E. Wilson, J. Chem. Soc. A: Inorg., Phys. Theor., 4, 2209 (1968); https://doi.org/10.1039/j19680002209
  33. W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
  34. A. Apelblat, J. Solution Chem., 40, 1234 (2011); https://doi.org/10.1007/s10953-011-9718-y
  35. M.L. Petrus, R.K.M. Bouwer, U. Lafont, S. Athanasopoulos, N.C. Greenham and T.J. Dingemans, J. Mater. Chem. A Mater. Energy Sustain., 2, 9474 (2014); https://doi.org/10.1039/C4TA01629G
  36. T.P. Yoon and E.N. Jacobsen, Science, 299, 1691 (2003); https://doi.org/10.1126/science.1083622
  37. R. Nair, A. Shah, S. Baluja and S. Chanda, J. Serb. Chem. Soc., 71, 733 (2006); https://doi.org/10.2298/JSC0607733N
  38. W.G. Hanna and M.M. Moawad, Transition Met. Chem., 26, 644 (2001); https://doi.org/10.1023/A:1012066612090
  39. P.A. Vigato and S. Tamburini, Coord. Chem. Rev., 248, 1717 (2004); https://doi.org/10.1016/j.cct.2003.09.003
  40. S. Ilhan, H. Baykara, M.S. Seyitoglu, A. Levent, S. Özdemir, A. Dündar, A. Öztomsuk and M.H. Cornejo, J. Mol. Struct., 1075, 32 (2014); https://doi.org/10.1016/j.molstruc.2014.06.062
  41. M. Gaber, N. El-Wakiel, H. El-Ghamry and S.K. Fathalla, J. Mol. Struct., 1076, 251 (2014); https://doi.org/10.1016/j.molstruc.2014.06.071
  42. A. Kakanejadifard, F. Esna-ashari, P. Hashemi and A. Zabardasti, Spectrochim. Acta A Mol. Biomol. Spectrosc., 106, 80 (2013); https://doi.org/10.1016/j.saa.2012.12.044
  43. S. Deepak Chouhan, K.K. Verma and S. Garg, Chem. Sci. Trans., 6, 448 (2017).
  44. G. Goyat, S. Garg and K.K. Verma, Chem. Sci. Trans., 5, 479 (2016).
  45. S. Deepak Chouhan, K.K. Verma and S. Garg, Int. J. Chem. Sci., 14, 269 (2016).
  46. A. Pui, T. Malutan, L. Tataru, C. Malutan, D. Humelnicu and G. Carja, Polyhedron, 30, 2127 (2011); https://doi.org/10.1016/j.poly.2011.05.029
  47. O.M. Ali, Spectrochim. Acta A, 132, 52 (2014); https://doi.org/10.1016/j.saa.2014.03.127
  48. A.A. Abdel-Aziz, A.N. Salem, M.A. Sayed and M.M. Aboaly, J. Mol. Struct., 1010, 130 (2012); https://doi.org/10.1016/j.molstruc.2011.11.043
  49. D. Dey, G. Kaur, A. Ranjani, L. Gayathri, P. Chakraborty, J. Adhikary, J. Pasan, D. Dhanasekaran, A.R. Choudhury, M.A. Akbarsha, N. Kole and B. Biswas, Eur. J. Inorg. Chem., 2014, 3350 (2014); https://doi.org/10.1002/ejic.201402158
  50. M.M. Aboaly and M.M.H. Khalil, Spectrosc. Lett., 34, 495 (2001); https://doi.org/10.1081/SL-100105095
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