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Aromatik Schiff Bazları ve Co(II), Ni(II) ve Cu(II) Komplekslerinin Sentezi: Antimikrobiyal Aktivitelerinin İncelenmesi

Year 2022, Volume: 9 Issue: 3, 1049 - 1070, 30.09.2022
https://doi.org/10.31202/ecjse.1099521

Abstract

N,N-dietil-p-fenilendiamin ile salisilaldehit ve 2,4-dihidroksibenzaldehit ayrı ayrı reaksiyona sokulup, iki farklı türde Schiff bazı ligantları sentezlenmiştir. Elde edilen ligandların, Co(II), Cu(II) ve Ni(II) kompleksleri sentezlenmiş ve sentezlenen ligand ve metal komplekslerinin yapıları, FT-IR, UV.-Vis., ICP-OES, TG/DTA/DTG, 1H ve 13C NMR ve elemental analiz (C, H, N ve metal içeriği) teknikleri kullanılarak karakterize edilmiştir. Çalışmada elde edilen ligandların ve metal komplekslerin gram pozitif; Staphylococcus aureus Rosenbach ATCC-6538, Bacillus cereus ATCC 7064, gram negatif; Escherichia coli ATCC-8739, Salmonella typhimurium ve Candida albicans ATCC-90028 maya suşuna karşı biyolojik aktiviteleri incelenmiştir. L1 ligand ve komplekslerinin mikroorganizmalara karşı 8,15-12,99 mm, L2 ve komplekslerinin mikroorganizmalara karşı 7,66-13,88 mm çapında inhibisyon zonları gösterdiği belirlenmiştir. Elde edilen bu kompleks yapıların gram negatif ve gram pozitif suşlara karşı olumlu etkisi bulunduğundan hayatımızda yoğun olarak kullanılan antibiyotiklere alternatif olması mümkündür.

Supporting Institution

Kahramanmaraş Sütçü İmam Üniversitesi

Project Number

2021/2-7 YLS, 2019/2-17 YLS

References

  • [1] M. Sadia, J. Khan, R. Naz, M. Zahoor, S. Wadood Ali Shah, R. Ullah, S. Naz, A. Bari, H. Majid Mahmood, S. Saeed Ali, S.A. Ansari, M. Sohaib, Schiff base ligand L synthesis and its evaluation as anticancer and antidepressant agent, J. King Saud Univ. - Sci. 33 (2021) 101331. https://doi.org/10.1016/j.jksus.2020.101331.
  • [2] T.A. Alorini, A.N. Al-Hakimi, S. El-Sayed Saeed, E.H.L. Alhamzi, A.E.A.E. Albadri, Synthesis, characterization, and anticancer activity of some metal complexes with a new Schiff base ligand, Arab. J. Chem. 15 (2022) 103559. https://doi.org/10.1016/j.arabjc.2021.103559.
  • [3] S.G. Nozha, S.M. Morgan, S.E.A. Ahmed, M.A. El-Mogazy, M.A. Diab, A.Z. El-Sonbati, M.I. Abou-Dobara, Polymer complexes. LXXIV. Synthesis, characterization and antimicrobial activity studies of polymer complexes of some transition metals with bis-bidentate Schiff base, J. Mol. Struct. 1227 (2021) 129525. https://doi.org/10.1016/j.molstruc.2020.129525.
  • [4] T. Maharana, N. Nath, H.C. Pradhan, S. Mantri, A. Routaray, A.K. Sutar, Polymer-supported first-row transition metal schiff base complexes: Efficient catalysts for epoxidation of alkenes, React. Funct. Polym. 171 (2022) 105142. https://doi.org/10.1016/j.reactfunctpolym.2021.105142.
  • [5] J. Costamagna, J. Vargas, R. Latorre, A. Alvarado, G. Mena, Coordination compounds of copper, nickel and iron with Schiff bases derived from hydroxynaphthaldehydes and salicylaldehydes, Coord. Chem. Rev. 119 (1992) 67–88. https://doi.org/https://doi.org/10.1016/0010-8545(92)80030-U.
  • [6] M. Balouiri, M. Sadiki, S.K. Ibnsouda, Methods for in vitro evaluating antimicrobial activity: A review, J. Pharm. Anal. 6 (2016) 71–79. https://doi.org/10.1016/j.jpha.2015.11.005.
  • [7] A.W. Bauer, W.M.M. Kirby, J.C. Sherris, M. Turck, Antibiotic Susceptibility Testing by a Standardized Single Disk Method, Am. J. Clin. Pathol. 45 (1966) 493–496. https://doi.org/10.1093/ajcp/45.4_ts.493.
  • [8] V.S. Sharma, A.P. Shah, A.S. Sharma, A new class of supramolecular liquid crystals derived from azo calix[4]arene functionalized 1,3,4-thiadiazole derivatives, New J. Chem. 43 (2019) 3556–3564. https://doi.org/10.1039/C8NJ04997A.
  • [9] L. Zhu, Q. Zhu, J. Zhao, C. Dai, Investigation of thermal properties and growth mechanisms of nano-porous calix[4]arenes, Nanosci. Nanotechnol. Lett. 7 (2015) 939–944. https://doi.org/10.1166/nnl.2015.2049.
  • [10] T. Paul, M.F. Hossen, M.K.-E.- Zahan, M.M. Haque, R. Zamir, M.A. Asraf, Structural Investigation and Antibacterial Activity of Cu(II), Co(II), Ni(II) and Zn(II) Complexes of a Schiff Base Derived from Salicylaldehyde and Thiosemicarbazide, Asian J. Appl. Chem. Res. (2020) 39–48. https://doi.org/10.9734/ajacr/2020/v5i330138.

Synthesis of Aromatic Schiff Bases and Co(II), Ni(II) and Cu(II) Complexes: Investigation of Antımicrobial Activities

Year 2022, Volume: 9 Issue: 3, 1049 - 1070, 30.09.2022
https://doi.org/10.31202/ecjse.1099521

Abstract

Two types of Schiff base ligands were synthesized with the reaction of N,N-diethyl-p-phenylenediamine and salicylaldehyde , 2,4-dihydroxybenzaldehyde separately. Co(II), Cu(II), Ni(II) complexes of the obtained ligants were synthesized and characterized using FT-IR, UV.-Vis., ICP-OES, TG/DTA/DTG, 1H and 13C NMR) and elemental analyses (C, H, N and metal contents analyses). The ligands and metal complexes obtained in the study were gram positive; Staphylococcus aureus Rosenbach ATCC-6538, Bacillus cereus ATCC 7064, gram negative; Escherichia coli ATCC-8739, Salmonella typhimurium and Candida albicans ATCC-90028 yeast strain biological activities against were investigated. It was determined that the L1 ligand and its complexes showed 8.15-12.99 mm diameter inhibition zones against microorganisms, and the L2 and complexes showed 7.66-13.88 mm diameter inhibition zones against microorganisms. Since these complex structures have positive effects against gram-negative and gram-positive strains, it is possible to be an alternative to antibiotics that are used extensively in our lives.

Project Number

2021/2-7 YLS, 2019/2-17 YLS

References

  • [1] M. Sadia, J. Khan, R. Naz, M. Zahoor, S. Wadood Ali Shah, R. Ullah, S. Naz, A. Bari, H. Majid Mahmood, S. Saeed Ali, S.A. Ansari, M. Sohaib, Schiff base ligand L synthesis and its evaluation as anticancer and antidepressant agent, J. King Saud Univ. - Sci. 33 (2021) 101331. https://doi.org/10.1016/j.jksus.2020.101331.
  • [2] T.A. Alorini, A.N. Al-Hakimi, S. El-Sayed Saeed, E.H.L. Alhamzi, A.E.A.E. Albadri, Synthesis, characterization, and anticancer activity of some metal complexes with a new Schiff base ligand, Arab. J. Chem. 15 (2022) 103559. https://doi.org/10.1016/j.arabjc.2021.103559.
  • [3] S.G. Nozha, S.M. Morgan, S.E.A. Ahmed, M.A. El-Mogazy, M.A. Diab, A.Z. El-Sonbati, M.I. Abou-Dobara, Polymer complexes. LXXIV. Synthesis, characterization and antimicrobial activity studies of polymer complexes of some transition metals with bis-bidentate Schiff base, J. Mol. Struct. 1227 (2021) 129525. https://doi.org/10.1016/j.molstruc.2020.129525.
  • [4] T. Maharana, N. Nath, H.C. Pradhan, S. Mantri, A. Routaray, A.K. Sutar, Polymer-supported first-row transition metal schiff base complexes: Efficient catalysts for epoxidation of alkenes, React. Funct. Polym. 171 (2022) 105142. https://doi.org/10.1016/j.reactfunctpolym.2021.105142.
  • [5] J. Costamagna, J. Vargas, R. Latorre, A. Alvarado, G. Mena, Coordination compounds of copper, nickel and iron with Schiff bases derived from hydroxynaphthaldehydes and salicylaldehydes, Coord. Chem. Rev. 119 (1992) 67–88. https://doi.org/https://doi.org/10.1016/0010-8545(92)80030-U.
  • [6] M. Balouiri, M. Sadiki, S.K. Ibnsouda, Methods for in vitro evaluating antimicrobial activity: A review, J. Pharm. Anal. 6 (2016) 71–79. https://doi.org/10.1016/j.jpha.2015.11.005.
  • [7] A.W. Bauer, W.M.M. Kirby, J.C. Sherris, M. Turck, Antibiotic Susceptibility Testing by a Standardized Single Disk Method, Am. J. Clin. Pathol. 45 (1966) 493–496. https://doi.org/10.1093/ajcp/45.4_ts.493.
  • [8] V.S. Sharma, A.P. Shah, A.S. Sharma, A new class of supramolecular liquid crystals derived from azo calix[4]arene functionalized 1,3,4-thiadiazole derivatives, New J. Chem. 43 (2019) 3556–3564. https://doi.org/10.1039/C8NJ04997A.
  • [9] L. Zhu, Q. Zhu, J. Zhao, C. Dai, Investigation of thermal properties and growth mechanisms of nano-porous calix[4]arenes, Nanosci. Nanotechnol. Lett. 7 (2015) 939–944. https://doi.org/10.1166/nnl.2015.2049.
  • [10] T. Paul, M.F. Hossen, M.K.-E.- Zahan, M.M. Haque, R. Zamir, M.A. Asraf, Structural Investigation and Antibacterial Activity of Cu(II), Co(II), Ni(II) and Zn(II) Complexes of a Schiff Base Derived from Salicylaldehyde and Thiosemicarbazide, Asian J. Appl. Chem. Res. (2020) 39–48. https://doi.org/10.9734/ajacr/2020/v5i330138.
There are 10 citations in total.

Details

Primary Language Turkish
Subjects Engineering
Journal Section Makaleler
Authors

Serhan Uruş 0000-0002-4204-9860

Project Number 2021/2-7 YLS, 2019/2-17 YLS
Publication Date September 30, 2022
Submission Date April 6, 2022
Acceptance Date July 7, 2022
Published in Issue Year 2022 Volume: 9 Issue: 3

Cite

IEEE S. Uruş, “Aromatik Schiff Bazları ve Co(II), Ni(II) ve Cu(II) Komplekslerinin Sentezi: Antimikrobiyal Aktivitelerinin İncelenmesi”, El-Cezeri Journal of Science and Engineering, vol. 9, no. 3, pp. 1049–1070, 2022, doi: 10.31202/ecjse.1099521.
Creative Commons License El-Cezeri is licensed to the public under a Creative Commons Attribution 4.0 license.
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