Synthesis, Spectral Characterization, Electrochemical, Antioxidant and Antimicrobial Evaluation of 3d-Metal Complexes of 3-Mercapto-4-(Pyren-1-ylmethylene)Amino-1,2,4-Triazin-5-One

References

• Y. Lukmantara, D.S. Kalinowski, N. Kumar, and D.R. Richardson, “Synthesis and Biological Evaluation of 2-Benzoylpyridine Thiosemicarbazones in a Dimeric System: Structure-Activity Relationship Studies on Their anti-Proliferative and Iron Chelation Efficacy,” Journal of Inorganic Biochemistry 141, no. 1 (2014): 43–54.
   PubMedGoogle Scholar
• N.V. Kulkarni, N.H. Bevinahalli, and V.K. Revankar, “Ligational behavior of S, N, and O Donor Quinoxaline Derivatives toward the Later First-Row Transition Metal Ions,” Journal of Coordination Chemistry 63, no. 10 (2010): 1785–94.
   Web of Science ®Google Scholar
• M. Shebl, “Coordination behavior of New Bis(Tridentate ONO, ONS and ONN) Donor Hydrazones towards Some Transition Metal Ions: Synthesis, Spectral, Thermal, Antimicrobial and Antitumor Studies,” Journal of Molecular Structure 1128 (2017): 79–93.
   Web of Science ®Google Scholar
• Z.H. Xu, X.W. Zhang, W.Q. Zhang, Y.H. Gao, and Z.Z. Zeng, “Synthesis, Characterization, DNA Interaction and Antibacterial Activities of Two Tetranuclear Cobalt(II) and Nickel(II) Complexes with Salicylaldehyde 2-Phenylquinoline-4-Carboylhydrazone,” Inorganic Chemistry Communications 14, no. 10 (2011): 1569–73.
   Web of Science ®Google Scholar
• A.A. Al-Amiery, A.A.H. Kadhum, and A.B. Mohamad, “Antifungal and Antioxidant Activities of Pyrrolidone Thiosemicarbazone Complexes,” Bioinorganic Chemistry and Applications 2012 (2012): 1–6.
   Web of Science ®Google Scholar
• S. Kumar, D.N. Dhar, and P.N. Saxena, “Applications of Metal Complexes of Schiff bases-A Review,” Journal of Scientific and Industrial Research 68, no. 3 (2009): 181–7.
   Web of Science ®Google Scholar
• J. Costamagna, G. Ferraudi, B. Matsuhiro, M. Campos-Vallette, J. Canales, M. Villagrán, J. Vargas, and M.J. Aguirre, “Complexes of Macrocycles with Pendant Arms as Models for Biological Molecules,” Coordination Chemistry Reviews 196, no. 1 (2000): 125–64.
   Google Scholar
• A. Prakash and D. Adhikari, “Application of Schiff Bases and Their Metal complexes-A Review,” International Journal of ChemTech Research 3, no. 4 (2011): 1891–6.
   Google Scholar
• T. Joseph, D.P. Sawant, C.S. Gopinath, and S.B. Halligudi, “Zeolite encapsulated Ruthenium and Cobalt Schiff Base Complexes Catalyzed Allylic Oxidation of α-Pinene,” Journal of Molecular Catalysis A: Chemical 184, no. 1–2 (2002): 289–99.
   Google Scholar
• Y.D.M. Champouret, J. Fawcett, W.J. Nodes, K. Singh, and G.A. Solan, “Spacially confined M2 Centers (M = Fe, Co, Ni, Zn) on a Sterically Bulky Binucleating Support: Synthesis, Structures and Ethylene Oligomerization Studies,” Inorganic chemistry 45, no. 24 (2006): 9890–900.
   PubMed Web of Science ®Google Scholar
• A.L. Berhanu, Gaurav, I. Mohiuddin, A.K. Malik, J.S. Aulakh, V. Kumar, and K.-H. Kim, “A Review of the Applications of Schiff Bases as Optical Chemical Sensors,” TrAC Trends in Analytical Chemistry 116 (2019): 74–91.
   Web of Science ®Google Scholar
• J.C. Berrones-Reyes, B.M. Muñoz-Flores, A.M. Cantón-Diáz, M.A. Treto-Suárez, D. Páez-Hernández, E. Schott, X. Zarate, and V.M. Jiménez-Pérez, “Quantum chemical Elucidation of the Turn-on Luminescence Mechanism in Two New Schiff Bases as Selective Chemosensors of Zn2+: Synthesis, Theory and Bioimaging Applications,” RSC advances 9, no. 53 (2019): 30778–89.
   PubMed Web of Science ®Google Scholar
• K. Singh, S. Raparia, and S. Raparia, “Synthesis, Characterization and Biological Evaluation of Triazine Based Schiff Base Metal Complexes,” European Chemical Bulletin 5 (2016): 92–8.
   Google Scholar
• K. Singh, R. Thakur, and G. Kumar, “Synthesis, Characterization and in Vitro Anticancer Activity of Co(II), Ni(II), Cu(II), and Zn(II) Complexes with 4-[{3-(4-Bromophenyl)-1-Phenyl-1h-Pyrazol-4-Ylmethylene}-Amino]-3-Mercapto-1,2,4-Triazin-5-One,” European Chemical Bulletin 5 (2016): 46–53.
   Google Scholar
• K. Singh, S. Raparia, and P. Surain, “Co(II), Ni(II), Cu(II) and Zn(II) Complexes of 4-(4-Cyanobenzylideneamino)-3-Mercapto-5-Oxo-1,2,4-Triazine: Synthesis, Characterization and Biological Studies,” Medicinal Chemistry Research 24, no. 6 (2015): 2336–46.
   Web of Science ®Google Scholar
• K. Singh,   Ritu, and V. Kumar, “Spectral, Thermal, Fluorescence and Antimicrobial Studies of Some Newly Synthesized Metal Complexes,” Journal of Chemical, Biological and Physical Sciences 5, no. 3 (2015): 2691–705.
   Google Scholar
• Z.L. Yuan, L. Wang, X.M. Shen, X.Q. Yang, J.D. Huang, and G. Wei, “Copper(II) and Platinum(II) Compounds with Pyrene-Appended Dipicolylamine Ligand: Syntheses, Crystal Structures and Biological Evaluation,” Journal of Inclusion Phenomena and Macrocyclic Chemistry 82, no. 1–2 (2015): 135–43.
   Web of Science ®Google Scholar
• J. Lasri, S.M. Soliman, S.E. Elsilk, M. Haukka, and A. El-Faham, “Synthesis, Crystal Structure, DFT and Biological Activity of E-Pyrene-1-Carbaldehyde Oxime and E-2-Naphthaldehyde Oxime,” Journal of Molecular Structure 1207 (2020): 127848.
   Web of Science ®Google Scholar
• N.K. Gondia and S.K. Sharma, “Comparative optical Studies of Naphthalene Based Schiff Base Complexes for Colour Tunable Application,” Materials Chemistry and Physics 224, no. 2018 (2019): 314–9.
   Google Scholar
• S. Shaygan, H. Pasdar, N. Foroughifar, M. Davallo, and F. Motiee, “Cobalt (II) Complexes with Schiffbase Ligands Derived from Terephthalaldehyde and Ortho-Substituted Anilines: Synthesis, Characterization and Antibacterial Activity,” Applied Sciences 8, no. 3 (2018): 385.
   Google Scholar
• S. Dinda, S.C. Patra, and S. Ganguly, “Rhodium(III) Complex with Pyrene-Pyridyl-Hydrazone: synthesis, Structure, Ligand Redox, Spectral Characterization and DFT Calculation,” Journal of Chemical Sciences 131, no. 3 (2019): 1–9.
   Web of Science ®Google Scholar
• A. Gümüş, V. Okumuş, and S. Gümüş, “Synthesis, Biological Evaluation of Antioxidant-Antibacterial Activities and Computational Studies of New anthracene- And Pyrene-Based Schiff Base Derivatives,” Turkish journal of Chemistry 44, no. 4 (2020): 1200–15.
   PubMed Web of Science ®Google Scholar
• M. Heidelberger and H.P. Treffers, “Quantitative chemical Studies on Hemolysins: I. The Estimation of Total Antibody in Antisera to Sheep Erythrocytes and Stromata,” The Journal of General Physiology 25, no. 4 (1942): 523–31.
   PubMedGoogle Scholar
• A. Murugappan, J.S. Sudarsan, and A. Manoharan, “Effects of Using Lignite Mine Drainage for Irrigation on soils – A Case Study of Perumal Tank Command Area in Tamilnadu State,” Journal of Industrial Pollution Control 22, no. 1 (2006): 149–60.
   Google Scholar
• I. Ahmad, and A.Z. Beg, “Antimicrobial and Phytochemical Studies on 45 Indian Medicinal Plants against Multi-Drug Resistant Human Pathogens,” Journal of Ethnopharmacology 74, no. 2 (2001): 113–23.
   PubMed Web of Science ®Google Scholar
• I. Wiegand, K. Hilpert, and R.E.W. Hancock, “Agar and Broth Dilution Methods to Determine the Minimal Inhibitory Concentration (MIC) of Antimicrobial Substances,” Nature protocols 3, no. 2 (2008): 163–75.
   PubMed Web of Science ®Google Scholar
• K.T. Tadele, “Antioxidant Activity of Schiff Bases and Their Metal Complexes : A Recent Review,” Journal of Pharmaceutical and Medicinal Research 3, no. 1 (2017): 73–7.
   Google Scholar
• I. Ali, W.A. Wani, and K. Saleem, “Empirical formulae to Molecular Structures of Metal Complexes by Molar Conductance,” Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry 43, no. 9 (2013): 1162–70.
   Web of Science ®Google Scholar
• S. Chandra, and A.K. Sharma, “Nickel(II) and Copper(II) Complexes with Schiff Base Ligand 2,6-Diacetylpyridine Bis(Carbohydrazone): Synthesis and IR, Mass, 1H NMR, Electronic and EPR Spectral Studies,” Spectrochimica acta-Part A, Molecular and Biomolecular Spectroscopy 72, no. 4 (2009): 851–7.
   PubMed Web of Science ®Google Scholar
• K. Singh, P. Turk, and A. Dhanda, “Synthesis, Structural and Biological Studies of Co(II), Ni(II), Cu(II) and Zn(II) Complexes of 4-[(3-Ethoxy-4-Hydroxybenzylidene)Amino]-3-Mercapto-6-Methyl-5-Oxo-1,2,4-Triazine,” European Chemical Bulletin 7, no. 7 (2018): 194–202.
   Google Scholar
• P. Bharati, A. Bharti, P. Nath, S. Kumari, N.K. Singh, and M.K. Bharty, “Square planar Pd(II) Complexes Derived from 1-Ethyl-3-Phenylthiourea, 3-Mercapto-4-Methyl-1,2,4-Triazole and 2-Mercapto-5-Methyl-1,3,4-Thiadiazole: Syntheses, Spectral, Structural Characterization and Photoluminescence Properties,” Inorganica Chimica Acta 443 (2016): 160–9.
   Web of Science ®Google Scholar
• K. Singh, B. Kumari, and A. Sharma, “Synthesis, Spectral Characterisation and Biological Studies of Ni (II), Cu (II), Zn (II) and Cd (II) Complexes with 1, 2, 4-Triazole Based Bidentate Schiff Base,” Rasayan Journal of Chemistry 14, no. 01 (2021): 29–35.
   Google Scholar
• K. Singh and P. Siwach, “Metal based Bio-Active 1, 2, 4 Triazole Derivatives: Preparation, Spectral, Thermal and Antimicrobial Studies,” Chemical Biology Letters 9, no. 4 (2022): 407.
   Web of Science ®Google Scholar
• F. Samy and M. Shebl, “Synthesis, Spectroscopic, Biological, and Theoretical Studies of New Complexes from (E)‐3‐(2‐(5, 6‐Diphenyl‐1, 2, 4‐Triazin‐3‐yl) Hydrazono) Butan‐2‐One Oxime,” Applied Organometallic Chemistry 34, no. 4 (2020): e5502.
   Web of Science ®Google Scholar
• F. Samy and M. Shebl, “Co (II), Ni (II), and Cu (II) Complexes of 4, 6‐Bis (2‐Hydroxynaphthalen‐1‐yl) Methyl‐Ene) Hydrazono) Ethyl) Benzene‐1, 3‐Diol: Synthesis, Spectroscopic, Biological, and Theoretical Studies,” Applied Organometallic Chemistry 36, no. 5 (2022): e6650.
   Web of Science ®Google Scholar
• K. Singh, B. Kumari, and A. Sharma, “Copper(II), Nickel(II), Zinc(II) and Cadmium(II) Complexes of 1,2,4-Triazole Based Schiff Base Ligand: synthesis, Comparative Spectroscopic, Thermal, Biological and Molecular Docking Studies,” Spectroscopy Letters 54, no. 10 (2021): 742–62.
   Web of Science ®Google Scholar
• Z.H. Chohan, “Synthesis, Characterization, and Biological Properties of Bivalent Transition Metal Complexes of Co(II), Cu(II), Ni(II), and Zn(II) with Some Acylhydrazine Derived Furanyl and Thienyl ONO and SNO Donor Schiff Base Ligands,” Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 31, no. 1 (2001): 1–16.
   Web of Science ®Google Scholar
• N. Raman, Y.P. Raja, and A. Kulandaisamy, “Synthesis and Characterisation of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Schiff Base Complexes Derived from o-Phenylenediamine and Acetoacetanilide,” Journal of Chemical Sciences 113, no. 3 (2001): 183–9.
   Google Scholar
• M.A. Duncan, Infrared Spectroscopy of Transition Metal-Molecular Interactions in the Gas Phase (Athens, GA: University of Georgia, 2008), 4658–4.
   Google Scholar
• J. Fujita, K. Nakamoto, and M. Kobayashi, “Infrared Spectra of Metallic Complexes. II. The Absorption Bands of Coördinated Water in Aquo Complexes,” Journal of the American Chemical Society 78, no. 16 (1956): 3963–5.
   Web of Science ®Google Scholar
• K. Singh, P. Turk, and A. Dhanda, “Synthesis, Spectral Characterization, and Antimicrobial Evaluation of New Imine Derived from 3-Methylthiophene- 2-Carboxaldehyde and Its Co(II),” Ni(II), Cu(II), and Zn(II) Metal Complexes”. Applied Organometallic Chemistry 35 (2021): 1–14.
   Web of Science ®Google Scholar
• C.C.R. Sutton, G.D. Silva, and G.V. Franks, “Modeling the IR Spectra of Aqueous Metal Carboxylate Complexes: Correlation between Bonding Geometry and Stretching Mode Wavenumber Shifts,” Chemistry 21, no. 18 (2015): 6801–5.
   PubMed Web of Science ®Google Scholar
• S.M.E. Khalil, M. Shebl, and F.S. Al-Gohani, “Zinc (II) Thiosemicarbazone Complex as a Ligand towards Some Transition Metal Ions: synthesis, Spectroscopic and Antimicrobial Studies,” Acta chimica Slovenica 57, no. 3 (2010): 716–25.
   PubMed Web of Science ®Google Scholar
• H.F. El-Shafiy and M. Shebl, “Binuclear oxovanadium (IV), Cerium (III) and Dioxouranium (VI) Nano Complexes of a Bis (Bidentate) Ligand: Synthesis, Spectroscopic, Thermal, DFT Calculations and Biological Studies,” Journal of Molecular Structure 1194 (2019): 187–203.
   Web of Science ®Google Scholar
• K. Singh, R. Thakur, and V. Kumar, “Co(II), Ni(II), Cu(II), and Zn(II) Complexes Derived from 4-[{3-(4-Bromophenyl)-1-Phenyl-1H-Pyrazol-4-Ylmethylene}-Amino]-3-Mercapto-6-Methyl-5-Oxo-1,2,4-Triazine,” Beni-Suef University Journal of Basic and Applied Sciences 5, no. 1 (2016): 21–30.
   Google Scholar
• K.S. Shambuling, G.Y. Nagesh, K.R. Sumangala, and K.M. Neelakanthayya, “Synthesis, Characterization and Antimicrobial Activity of Metal Complexes Derived from Thiazole and 2-Naphthaldehyde,” Journal of Applied Chemistry 8, no. 4 (2015): 42–6.
   Google Scholar
• R. Fekri, M. Salehi, A. Asadi, and M. Kubicki, “Synthesis, Characterization, Anticancer and Antibacterial Evaluation of Schiff Base Ligands Derived from Hydrazone and Their Transition Metal Complexes,” Inorganica Chimica Acta 484 (2019): 245–54.
   Web of Science ®Google Scholar
• A.S. Munde, A.N. Jagdale, S.M. Jadhav, and T.K. Chondhekar, “Synthesis, Characterization and Thermal Study of Some Transition Metal Complexes of an Asymmetrical Tetradentate Schiff Base Ligand,” Journal of the Serbian Chemical Society 75, no. 3 (2010): 349–59.
   Web of Science ®Google Scholar
• A.E. Underhill and D.E. Billing, “Calculation of the Racah Parameter B for Nickel(II) and Cobalt(II) Compounds,” Nature 210, no. 5038 (1966): 834–5.
   Web of Science ®Google Scholar
• M.B. Fugu, N.P. Ndahi, B.B. Paul, and A.N. Mustapha, “Synthesis, Characterization, and Antimicrobial Studies of Some Vanillin Schiff Base Metal (II) Complexes,” Journal of Chemical and Pharmaceutical Research 5, no. 4 (2013): 22–8.
   Google Scholar
• V. Kumar, R.K. Singh, V. Kumari, B. Kumar, and S. Sharma, “Studies of Distorted Octahedral Complexes of Cobalt, Nickel and Copper and Their Antibacterial Properties,” Oriental Journal of Chemistry 34, no. 4 (2018): 1937–44.
   Web of Science ®Google Scholar
• B. Geeta, K. Shravankumar, P.M. Reddy, E. Ravikrishna, M. Sarangapani, K.K. Reddy, and V. Ravinder, “Binuclear cobalt(II), Nickel(II), Copper(II) and Palladium(II) Complexes of a New Schiff-Base as Ligand: Synthesis, Structural Characterization, and Antibacterial Activity,” Spectrochimica Acta–Part A, Molecular and Biomolecular Spectroscopy 77, no. 4 (2010): 911–5.
   PubMed Web of Science ®Google Scholar
• A.Z. El-Sonbati, M.A. Diab, and S.M. Morgan, “Thermal properties, Antimicrobial Activity and DNA Binding of Ni(II) Complexes of Azo Dye Compounds,” Journal of Molecular Liquids 225 (2017): 195–206.
   Web of Science ®Google Scholar
• N. Kavitha and P.V.A. Lakshmi, “Synthesis, Characterization and Thermogravimetric Analysis of Co(II), Ni(II), Cu(II) and Zn(II) Complexes Supported by ONNO Tetradentate Schiff Base Ligand Derived from Hydrazino Benzoxazine,” Journal of Saudi Chemical Society 21 (2017): S457–S466.
   Web of Science ®Google Scholar
• M. Shebl, S.M.E. Khalil, S.A. Ahmed, and H.A.A. Medien, “Synthesis, Spectroscopic Characterization and Antimicrobial Activity of Mono-, bi- and Tri-Nuclear Metal Complexes of a New Schiff Base Ligand,” Journal of Molecular Structure 980, no. 1–3 (2010): 39–50.
   Web of Science ®Google Scholar
• M. Shebl, “Synthesis, Spectral Studies, and Antimicrobial Activity of Binary and Ternary Cu(II), Ni(II), and Fe(III) Complexes of New Hexadentate Schiff Bases Derived from 4,6-Diacetylresorcinol and Amino Acids,” Journal of Coordination Chemistry 62, no. 19 (2009): 3217–31.
   Web of Science ®Google Scholar
• A.S. El-Tabl, “Synthesis and Physico-Chemical Studies on Cobalt(II), Nickel(II) and Copper(II) Complexes of Benzidine Diacetyloxime,” Transition Metal Chemistry 27, no. 2 (2002): 166–70.
   Web of Science ®Google Scholar
• J.C. Eisenstein, “Effect of Exchange Interaction on the Magnetic and Thermal Properties of Copper Salts and Copper Coordination Compounds,” The Journal of Chemical Physics 28, no. 2 (1958): 323–9.
   Web of Science ®Google Scholar
• D. Kivelson and R. Neiman, “ESR studies on the Bonding in Copper Complexes,” The Journal of Chemical Physics 35, no. 1 (1961): 149–55.
   Web of Science ®Google Scholar
• A.S. El-Tabl, M.M.E. Shakdofa, and A.M.A. El-Seidy, “Synthesis, Characterization and ESR Studies of New Copper(II) Complexes of Vicinal Oxime Ligands,” Journal of the Korean Chemical Society 55, no. 4 (2011): 603–11.
   Google Scholar
• R.K. Ray and G.B. Kauffman, “An EPR Study of Some Copper(II) Coordination Compounds of Substituted Biguanides. Part IV,” Inorganica Chimica Acta 174, no. 2 (1990): 257–62.
   Web of Science ®Google Scholar
• S.A. Patil, P.G. Avaji, and P.S. Badami, “Synthesis, Spectral, Thermal, Solid-State DC Electrical Conductivity and Biological Studies of Co(II) Complexes with Schiff Bases Derived from 3-Substituted-4-Amino-5-Hydrazino-1,2,4-Triazole and Substituted Salicylaldehydes,” Transition Metal Chemistry 33, no. 3 (2008): 275–83.
   Web of Science ®Google Scholar
• M. Sohrabi, M. Amirnasr, H. Farrokhpour, and S. Meghdadi, “A single Chemosensor with Combined Ionophore/Fluorophore Moieties Acting as a Fluorescent “off-on” Zn2+ Sensor and a Colorimetric Sensor for Cu2+: Experimental, Logic Gate Behavior and TD-DFT Calculations,” Sensors and Actuators B: Chemical 250 (2017): 647–58.
   Web of Science ®Google Scholar
• S.A. Patil, V.H. Naik, A.D. Kulkarni, and P.S. Badami, “DNA cleavage, Antimicrobial, Spectroscopic and Fluorescence Studies of Co(II), Ni(II) and Cu(II) Complexes with SNO Donor Coumarin Schiff Bases,” Spectrochimica Acta-Part A, Molecular and Biomolecular Spectroscopy 75, no. 1 (2010): 347–54.
   PubMed Web of Science ®Google Scholar
• T. Yu, K. Zhang, Y. Zhao, C. Yang, H. Zhang, L. Qian, D. Fan, W. Dong, L. Chen, and Y. Qiu, “Synthesis, Crystal Structure and Photoluminescent Properties of an Aromatic Bridged Schiff Base Ligand and Its Zinc Complex,” Inorganica Chimica Acta 361, no. 1 (2008): 233–40.
   Web of Science ®Google Scholar
• N.K. Gondia and S.K. Sharma, “Quantum yield and Photometric Parameters of Some Transition Metal Ion Schiff Base Complexes,” Optical and Quantum Electronics 49, no. 9 (2017): 1–12.
   Web of Science ®Google Scholar
• K. Singh, A. Kumar, R. Srivastava, P.S. Kadyan, M.N. Kamalasanan, and I. Singh, “Synthesis and Characterization of 5,7-Dimethyl-8-Hydroxyquinoline and 2-(2-Pyridyl)Benzimidazole Complexes of Zinc(II) for Optoelectronic Application,” Optical Materials 34, no. 1 (2011): 221–7.
   Web of Science ®Google Scholar
• M. Shebl, A.A. Saleh, S.M.E. Khalil, M. Dawy, and A.A.M. Ali, “Synthesis, Spectral, Magnetic, DFT Calculations, Antimicrobial Studies and Phenoxazinone Synthase Biomimetic Catalytic Activity of New Binary and Ternary Cu (II), Ni (II) and Co (II) Complexes of a Tridentate ONO Hydrazone Ligand,” Inorganic and Nano-Metal Chemistry 51, no. 2 (2021): 195–209.
   Web of Science ®Google Scholar
• M. Shebl, O.M. Adly, H.F. El-Shafiy, S.M.E. Khalil, A. Taha, and M.A. Mahdi, “Structural variety of Mono-and Binuclear Transition Metal Complexes of 3-[(2-Hydroxy-Benzylidene)-Hydrazono]-1-(2-Hydroxyphenyl)-Butan-1-One: synthesis, Spectral, Thermal, Molecular Modeling, Antimicrobial and Antitumor Studies,” Journal of Molecular Structure 1134 (2017): 649–60.
   Web of Science ®Google Scholar
• O.M. Adly, M. Shebl, E.M. Abdelrhman, and B.A. El-Shetary, “Synthesis, Spectroscopic, X-Ray Diffraction, Antimicrobial and Antitumor Studies of Ni (II) and Co (II) Complexes Derived from 4-Acetyl-5, 6-Diphenyl-3 (2H)-Pyridazinone and Ethylenediamine,” Journal of Molecular Structure 1219 (2020): 128607.
   Web of Science ®Google Scholar
• W. Al Zoubi, A.A.S. Al-Hamdani, and Y.G. Ko, “Schiff bases and Their Complexes: Recent Progress in Thermal Analysis,” Separation Science and Technology 52, no. 6 (2017): 1052–69.
   Web of Science ®Google Scholar
• S.M. Morgan, M.A. Diab, and A.Z. El-Sonbati, “Synthesis, Molecular Geometry, Spectroscopic Studies and Thermal Properties of Co(II) Complexes,” Applied Organometallic Chemistry 32, no. 4 (2018): e4305–16.
   Web of Science ®Google Scholar
• J. Zsako, “Kinetic Analysis of Thermogravimetric Data,” The Journal of Physical Chemistry 72, no. 7 (1968): 2406–11.
   Web of Science ®Google Scholar
• A.H. Kianfar, L. Keramat, M. Dostani, M. Shamsipur, M. Roushani, and F. Nikpour, “Synthesis, Spectroscopy, Electrochemistry and Thermal Study of Ni(II) and Cu(II) Unsymmetrical N 2O 2 Schiff Base Complexes,” Spectrochimica Acta-Part A, Molecular and Biomolecular Spectroscopy 77, no. 2 (2010): 424–9.
   PubMed Web of Science ®Google Scholar
• A. Abayneh, T. Gebretsadik, S. Tadesse, and M. Thomas, “Synthesis, Spectroscopic, Structural Characterization, Conductivity and Electrochemical Studies of a Schiff Base Ligand and Its Copper Complexes,” Advances in Chemical Engineering and Science 08, no. 04 (2018): 241–54.
   Google Scholar
• N. Elgrishi, K.J. Rountree, B.D. McCarthy, E.S. Rountree, T.T. Eisenhart, and J.L. Dempsey, “A Practical Beginner’s Guide to Cyclic Voltammetry,” Journal of Chemical Education 95, no. 2 (2018): 197–206.
   Web of Science ®Google Scholar
• J.N. Bavane and R.B. Mohod, “Synthesis, Characterization and Electrochemical Studies of Symmetrical Schiff Base Complexes of [1-(5-Chloro-2-Hydroxy-4-Methyl-Phenyl) Ethanone-4-Chloro(-3-Trifluromethyl)Aniline,” The Pharma Innovation 7, no. 1 (2018): 149–52.
   Google Scholar
• R.A. Shiekh, I.A. Rahman, M.A. Malik, N. Luddin, S.M. Masudi, and S.A. Al-Thabaiti, “Transition metal Complexes with Mixed Nitrogen-Sulphur (N-S) Donor Macrocyclic Schiff Base Ligand: Synthesis, Spectral, Electrochemical and Antimicrobial Studies,” International Journal of Electrochemical Science 8, no. 5 (2013): 6972–87.
   Web of Science ®Google Scholar
• V. Srinivasan, M.A. Jhonsi, N. Dhenadhayalan, K.C. Lin, D.A. Ananth, T. Sivasudha, R. Narayanaswamy, and A. Kathiravan, “Pyrene-Based Prospective Biomaterial: In Vitro Bioimaging, Protein Binding Studies and Detection of Bilirubin and Fe3,” Spectrochimica Acta-Part A, Molecular and Biomolecular Spectroscopy 221 (2019): 117150.
   PubMed Web of Science ®Google Scholar
• V. Srinivasan, T. Khamrang, C. Ponraj, D. Saravanan, R. Yamini, S. Bera, and M.A. Jhonsi, “Pyrene based Schiff Bases: Synthesis, Crystal Structure, Antibacterial and BSA Binding Studies,” Journal of Molecular Structure 1225 (2021): 129153.
   Web of Science ®Google Scholar
• H. Kargar, A.A. Ardakani, M.N. Tahir, M. Ashfaq, and K.S. Munawar, “Synthesis, Spectral Characterization, Crystal Structure Determination and Antimicrobial Activity of Ni(II), Cu(II) and Zn(II) Complexes with the Schiff Base Ligand Derived from 3, 5-Dibromosalicylaldehyde,” Journal of Molecular Structure 1229 (2021): 129842.
   Web of Science ®Google Scholar
• H. Kargar, M. Fallah-Mehrjardi, R. Behjatmanesh-Ardakani, H.A. Rudbari, A.A. Ardakani, S. Sedighi-Khavidak, K.S. Munawar, M. Ashfaq, and M.N. Tahir, “Binuclear Zn (II) Schiff Base Complexes: Synthesis, Spectral Characterization, Theoretical Studies and Antimicrobial Investigations,” Inorganica Chimica Acta 530 (2022): 120677.
   Web of Science ®Google Scholar
• A. Sahraei, H. Kargar, M. Hakimi, and M.N. Tahir, “Synthesis, Characterization, Crystal Structures and Biological Activities of Eight-Coordinate Zirconium (IV) Schiff Base Complexes,” Transition Metal Chemistry 42, no. 6 (2017): 483–9.
   Web of Science ®Google Scholar
• M. Shakir, S. Hanif, M.A. Sherwani, O. Mohammad, and S.I. Al-Resayes, “Pharmacologically significant Complexes of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) of New Schiff Base Ligand, (E)-N-(Furan-2-yl Methylene) Quinolin-8-Amine: Synthesis, Spectral, XRD, SEM, Antimicrobial, Antioxidant and in Vitro Cytotoxic Studies,” Journal of Molecular Structure 1092 (2015): 143–59.
   Web of Science ®Google Scholar