References
- Ajlouni, A. M., Abu-Salem, Q., Taha, Z. A., Hijazi, A. K., & Al Momani, W. (2016). Synthesis, characterization, biological activities and luminescent properties of lanthanide complexes with [2-thiophenecarboxylic acid, 2-(2-pyridinyl methylene)hydrazide] Schiff bases ligand. Journal of Rare Earths, 34(10), 986–993. https://doi.org/https://doi.org/10.1016/S1002-0721(16)60125-4
- Amarowicz, R., Pegg, R. B., Rahimi-Moghaddam, P., Barl, B., & Weil, J. A. (2004). Free-radical scavenging capacity and antioxidant activity of selected plant species from the Canadian prairies. Food Chemistry, 84(4), 551–562. https://doi.org/https://doi.org/10.1016/S0308-8146(03)00278-4
- Amr, A. E.-G E., Sayed, H. H., & Abdulla, M. M. (2005). Synthesis and reactions of some new substituted pyridine and pyrimidine derivatives as analgesic, anticonvulsant and antiparkinsonian agents. Archiv der Pharmazie, 338(9), 433–440. https://doi.org/https://doi.org/10.1002/ardp.200500982
- Andiappan, K., Sanmugam, A., Deivanayagam, E., Karuppasamy, K., Kim, H. S., & Vikraman, D. (2018). In vitro cytotoxicity activity of novel Schiff base ligand–lanthanide complexes. Scientific Reports, 8(1), 1–12.
- Arslan, H., Ozpozan, N., & Tarkan, N. (2002). Kinetic analysis of thermogravimetric data of p-toluidino-p-chlorophenylglyoxime and of some complexes. Thermochimica Acta, 383(1–2), 69–77. https://doi.org/https://doi.org/10.1016/S0040-6031(01)00657-8
- Azuara, L. R., & Gomez, M. E. B. (2010). Cu compounds in cancer chemotherapy. Current Medicinal Chemistry, 17(31), 3606–3615.
- Bard, A. J., & Faulkner, L. R. (1980). Electrochemical methods. John Wiley & Sons.
- Basu, C., Chowdhury, S., Banerjee, R., Evans, H. S., & Mukherjee, S. (2007). A novel blue luminescent high-spin Fe(III) complex with interlayer O–H⋯Cl bridging: Synthesis, structure and spectroscopic studies. Polyhedron, 26(14), 3617–3624. https://doi.org/https://doi.org/10.1016/j.poly.2007.03.053
- Bauer, A. W., Kirby, W. M., Sherris, J. C., & Turck, M. (1966). Antibiotic susceptibility testing by a standardized single disk method. American Journal of Clinical Pathology, 45(4), 493–496. https://doi.org/https://doi.org/10.1093/ajcp/45.4_ts.493
- Becke, A. D. (1992). Density‐functional thermochemistry. I. The effect of the exchange‐only gradient correction. Journal of Chemical Physics, 96(3), 2155–2160. https://doi.org/https://doi.org/10.1063/1.462066
- Beinert, H. (1977). Structure and function of copper proteins. Coordination Chemistry Reviews, 23(1), 119–129. https://doi.org/https://doi.org/10.1016/S0010-8545(00)80331-8
- Bellamy, L. J. (1969). Advances in infrared group frequencies. Methuen and Company, Ltd.
- Bencini, A., & Gattechi, D. (1990). EPR of exchange coupled system (Vol. 103, p. 627). Springer-Verlag.
- Clarke, M. J., Zhu, F., & Frasca, D. R. (1999). Non-platinum chemotherapeutic metallopharmaceuticals. Chemical Reviews, 99(9), 2511–2534. https://doi.org/https://doi.org/10.1021/cr9804238
- Cotton, F. A., & Wilkinson, G. (1986). Advanced inorganic chemistry: A comprehensive text (4th ed.). John Wiley & Sons.
- Criado, J. J., Manzano, J. L., & Rodrıguez-Fernandez, E. (2003). New organotropic compounds. Synthesis, characterization and reactivity of Pt(II) and Au(III) complexes with bile acids: DNA interactions and 'in vitro' anticancer activity. Journal of Inorganic Biochemistry, 96(2–3), 311–320. https://doi.org/https://doi.org/10.1016/s0162-0134(03)00240-x
- Cullity, B. D. (1978). Elements of X-ray diffraction (2nd ed.). Addison Wesley.
- Deacon, G. B., & Phillips, R. J. (1980). Relationships between the carbon–oxygen stretching frequencies of carboxylato complexes and the type of carboxylate coordination. Coordination Chemistry Reviews, 33(3), 227–250. https://doi.org/https://doi.org/10.1016/S0010-8545(00)80455-5
- Deschamps, P., Kulkarni, P. P., & Sarkar, B. (2003). The crystal structure of a novel copper(II) complex with asymmetric ligand derived from l-histidine. Inorganic Chemistry, 42(23), 7366–7368. https://doi.org/https://doi.org/10.1021/ic034760x
- Dudev, T., & Lim, C. (2000). Tetrahedral vs octahedral zinc complexes with ligands of biological interest: A DFT/CDM study. Journal of the American Chemical Society, 122(45), 11146–11153. https://doi.org/https://doi.org/10.1021/ja0010296
- Dutta, R. I., & Syamal, A. (1993). Elements of mageneto chemistry (2nd ed.). EWP.
- El-Dein, A. M., Libra, J. A., & Wiesmann, U. (2003). Mechanism and kinetic model for the decolorization of the azo dye Reactive Black 5 by hydrogen peroxide and UV radiation. Chemosphere, 52(6), 1069–1077. https://doi.org/https://doi.org/10.1016/S0045-6535(03)00226-1
- Emam, S. M. (2017). Spectral characterization, thermal and biological activity studies of Schiff base complexes derived from 4,4′-methylenedianiline, ethanol amine and benzil. Journal of Molecular Structure, 1134, 444–457. https://doi.org/https://doi.org/10.1016/j.molstruc.2016.12.071
- Faria, J. L. B., Almeida, F. M., Pilla, O., Rossi, F., Sasaki, J. M., Melo, F. E. A., Mendes, J. F., & Freire, P. T. C. (2004). Raman spectra of L-histidine hydrochloride monohydrate crystal. Journal of Raman Spectroscopy, 35(3), 242–248. https://doi.org/https://doi.org/10.1002/jrs.1142
- Fleming, I. (2010). Molecular orbitals and organic chemical reactions (1st ed.). John Wiley & Sons.
- Frisch, M. J., Trucks, G. W., Schlegel, H. B., Scuseria, G. E., Robb, M. A., Cheeseman, J. R., Scalmani, G., Barone, V., Mennucci, B., Petersson, G. A., Nakatsuji, H., Caricato, M., Li, X., Hratchian, H. P., Izmaylov, A. F., Bloino, J., Zheng, G., Sonnenberg, J. L., Hada, M., … Fox, D. J. (2009). Gaussian 09. Revision A.02. Gaussian, Inc.
- Geary, J. (1971). The use of conductivity measurements in organic solvents for the characterisation of coordination compounds. Coordination Chemistry Reviews, 7(1), 81–122. https://doi.org/https://doi.org/10.1016/S0010-8545(00)80009-0
- Hadi, A., Yaacob, I. I., & Gaik, C. S. (2006). Synthesis of nanocrystalline CeO2 using mechanochemical method: The effect of milling time on the particle size. Materials Science Forum, 517, 105–110. https://doi.org/https://doi.org/10.4028/www.scientific.net/MSF.517.105
- Hambley, T. W. (2007). Developing new metal-based therapeutics: Challenges and opportunities. Dalton Transactions, 49(43), 4929–4937. https://doi.org/https://doi.org/10.1039/b706075k
- Hathaway, B., & Billing, D. E. (1970). The electronic properties and stereochemistry of mono-nuclear complexes of the Cu(II) ion. Coordination Chemistry Reviews, 5(2), 143–207. https://doi.org/https://doi.org/10.1016/S0010-8545(00)80135-6
- Hay, P. J., & Wadt, W. R. (1985). Ab initio effective core potentials for molecular calculations. Potentials for the transition metal atoms Sc to Hg. Journal of Chemical Physics, 82(1), 270–283. https://doi.org/https://doi.org/10.1063/1.448799
- Jeyaraman, P., Alagarraj, A., & Natarajan, R. (2020). In silico and in vitro studies of transition metal complexes derived from curcumin-isoniazid Schiff base. Journal of Biomolecular Structure & Dynamics, 38(2), 488–499. https://doi.org/https://doi.org/10.1080/07391102.2019.1581090
- John, L., Joseyphus, R. S., & Joe, I. H. (2019). Synthesis, spectral characterization, DFT, and molecular docking studies of metal(II) complexes derived from thiophene-2-carboxaldehyde and 2-amino-6-picoline. Journal of Coordination Chemistry, 72(16), 2669–2687. https://doi.org/https://doi.org/10.1080/00958972.2019.1668929
- Johnson, J., & Dhanaraj, C. J. (2020). Biological and molecular modeling studies on some transition metal(II) complexes of a quinoxaline based ONO donor bishydrazone ligand. Journal of Biomolecular Structure & Dynamics, 1–16. https://doi.org/https://doi.org/10.1080/07391102.2020.1776637
- Karnan, M., Balachandran, V., Murugan, M., Murali, M. K., & Nataraj, A. (2013). Vibrational (FT-IR and FT-Raman) spectra, NBO, HOMO–LUMO, molecular electrostatic potential surface and computational analysis of 4-(trifluoromethyl)benzylbromide. Spectrochimica Acta: Part A, Molecular and Biomolecular Spectroscopy, 116, 84–95. https://doi.org/https://doi.org/10.1016/j.saa.2013.06.120
- Khan, M. I., Khan, A., Hussain, I., Khan, M. A., Gul, S., Iqbal, M., & Khuda, F. (2013). Spectral, XRD, SEM and biological properties of new mononuclear Schiff base transition metal complexes. Inorganic Chemistry Communications, 35, 104–109. https://doi.org/https://doi.org/10.1016/j.inoche.2013.06.014
- Kilveson, D. (1997). Publications of Daniel Kivelson. Journal of Physical Chemistry, 101(43), 8631–8634.
- Klein, R. A. (2006). Modified van der Waals atomic radii for hydrogen bonding based on electron density topology. Chemical Physics Letters, 425(1–3), 128–133. https://doi.org/https://doi.org/10.1016/j.cplett.2006.04.109
- Koksal, H., Tümer, M., & Serin, S. (1996). Synthesis and characterisation of binuclear Cu(II), Ni(II) and Co(II) chelates with tetradentate Schiff base ligands derived from 1,5-diaminonaphthalene. Synthesis and Reactivity in Inorganic and Metal–Organic Chemistry, 26(9), 1577–1588. https://doi.org/https://doi.org/10.1080/00945719608005148
- Kulkarni, A. D., & Truhlar, D. G. (2011). Performance of density functional theory and Møller–Plesset second-order perturbation theory for structural parameters in complexes of Ru . Journal of Chemical Theory and Computation, 7(7), 2325–2332. https://doi.org/https://doi.org/10.1021/ct200188n
- Kurumbail, R. G., Stevens, A. M., Gierse, J. K., McDonald, J. J., Stegeman, R. A., Pak, J. Y., Gildehaus, D., Miyashiro, J. M., Penning, T. D., Seibert, K., Isakson, P. C., & Stallings, W. C. (1996). Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents. Nature, 384(6610), 644–648. https://doi.org/https://doi.org/10.1038/384644a0
- Lever, A. B. P. (1984). Inorganic electronic spectroscopy (2nd ed.). Elsevier.
- Lone, I. H., Khan, K. Z., Fozdar, B. I., & Hussain, F. (2013). Synthesis antimicrobial and antioxidant studies of new oximes of steroidal chalcones. Steroids, 78(9), 945–950. https://doi.org/https://doi.org/10.1016/j.steroids.2013.05.015
- Lu, T., & Manzetti, S. (2014). Wavefunction and reactivity study of benzo[a] pyrene diol epoxide and its enantiomeric forms. Structural Chemistry, 25(5), 1521–1533. https://doi.org/https://doi.org/10.1007/s11224-014-0430-6
- Marzano, C., Pellei, M., Tisato, F., & Santini, C. (2009). Copper complexes as anticancer agents. Anti-Cancer Agents in Medicinal Chemistry, 9(2), 185–211. https://doi.org/https://doi.org/10.2174/187152009787313837
- Mishra, V. R., Ghanavatkar, C. W., Mali, S. N., Chaudhari, H. K., & Sekar, N. (2020). Schiff base clubbed benzothiazole: Synthesis, potent antimicrobial and MCF-7 anticancer activity, DNA cleavage and computational study. Journal of Biomolecular Structure & Dynamics, 38(6), 1772–1785. https://doi.org/https://doi.org/10.1080/07391102.2019.1621213
- Mizushima, Y., & Obayashi, M. K. (1968). Interaction of anti-inflammatory drugs with serum proteins, especially with some biologically active proteins. The Journal of Pharmacy and Pharmacology, 20(3), 169–173. https://doi.org/https://doi.org/10.1111/j.2042-7158.1968.tb09718.x
- Mohamed, G. G., Omar, M. M., & Hindy, A. M. (2005). Synthesis, characterization and biological activity of some transition metals with Schiff base derived from 2-thiophene carboxaldehyde and aminobenzoic acid. Spectrochimica Acta: Part A, Molecular and Biomolecular Spectroscopy, 62(4–5), 1140–1150. https://doi.org/https://doi.org/10.1016/j.saa.2005.03.031
- Morris, G. M., Huey, R., Lindstrom, W., Sanner, M. F., Belew, R. K., Goodsell, D. S., & Olson, A. J. (2009). AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility. Journal of Computational Chemistry, 30(16), 2785–2791. https://doi.org/https://doi.org/10.1002/jcc.21256
- Mosmann, T. (1983). Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. Journal of Immunological Methods, 65(1–2), 55–63. https://doi.org/https://doi.org/10.1016/0022-1759(83)90303-4
- Muller, J., Felix, K., Maichle, C., Lengfelder, E., Strähle, J., & Weser, U. (1995). Phenyl-substituted copper di-Schiff base, a potent Cu2Zn2 superoxide dismutase mimic surviving competitive biochelation. Inorganica Chimica Acta, 233(1–2), 11–19. https://doi.org/https://doi.org/10.1016/0020-1693(94)04298-A
- Nakamoto, K. (1997). Infrared spectra of inorganic and coordination compounds (5th ed.). Wiley Interscience.
- Orvig, C., & Abrams, M. J. (1999). Medicinal inorganic chemistry: Introduction. Chemical Reviews, 99(9), 2201–2204. https://doi.org/https://doi.org/10.1021/cr980419w
- Patil, S. A., Unki, S. N., Kulkarni, A. D., Naik, V. H., & Badami, P. S. (2011). Synthesis, characterization, in vitro antimicrobial and DNA cleavage studies of Co(II), Ni(II) and Cu(II) complexes with ONOO donor coumarin Schiff bases. Journal of Molecular Structure, 985(2–3), 330–338. https://doi.org/https://doi.org/10.1016/j.molstruc.2010.11.016
- Pravin, N., Kumaravel, G., Senthilkumar, R., & Raman, N. (2017). Water‐soluble Schiff base Cu(II) and Zn(II) complexes: Synthesis, DNA targeting ability and chemotherapeutic potential of Cu(II) complex for hepatocellular carcinoma – in vitro and in vivo approach. Applied Organometallic Chemistry, 31(10), e3739. https://doi.org/https://doi.org/10.1002/aoc.3739
- Rauf, M. A., & Ashraf, S. S. (2009). Fundamental principles and application of heterogeneous photocatalytic degradation of dyes in solution. Chemical Engineering Journal and the Biochemical Engineering Journal, 151(1–3), 10–18. https://doi.org/https://doi.org/10.1016/j.cej.2009.02.026
- Reddy, N. G., Krishna, P. M., & Kottam, N. (2015). Novel metal–organic photocatalysts: Synthesis, characterization and decomposition of organic dyes. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 137, 371–377. https://doi.org/https://doi.org/10.1016/j.saa.2014.08.045
- Reed, A. E., Weinstock, R. B., & Weinhold, F. (1985). Natural population analysis. Journal of Chemical Physics, 83(2), 735–746. https://doi.org/https://doi.org/10.1063/1.449486
- Refat, M. S., El-Sayed, M. Y., & Adam, A. M. A. (2013). Cu(II), Co(II) and Ni(II) complexes of new Schiff base ligand: Synthesis, thermal and spectroscopic characterizations. Journal of Molecular Structure, 1038, 62–72. https://doi.org/https://doi.org/10.1016/j.molstruc.2013.01.059
- Revathi, N., Sankarganesh, M., Dhaveethu Raja, J., Gujuluva Gangatharan, V. K., Arumugam, S., & Rajasekaran, R. (2020). Bio-active mixed ligand Cu(II) and Zn(II) complexes of pyrimidine derivative Schiff base: DFT calculation, antimicrobial, antioxidant, DNA binding, anticancer and molecular docking studies. Journal of Biomolecular Structure and Dynamics, 1–19.
- Sallam, S. A. (2006). Binuclear Cu(II), Ni(II) and Co(II) complexes with N2O2 chromophores of glycylglycine Schiff-bases of acetylacetone, benzoylacetone and thenoyltrifluoroacetone. Transition Metal Chemistry, 31(1), 46–55. https://doi.org/https://doi.org/10.1007/s11243-005-6312-4
- Sathyanarayana, D. N. (2001). Electronic absorption spectroscopy and related techniques. University Press.
- Sebastian, M., Arun, V., Robinson, P. P., Leeju, P., Varsha, G., Varghese, D., & Yusuff, K. K. M. (2011). Template synthesis and spectral characterization of some Schiff base complexes derived from quinoxaline-2-carboxaldehyde and L-histidine. Journal of Coordination Chemistry, 64(3), 525–533. https://doi.org/https://doi.org/10.1080/00958972.2010.549940
- Shahlaei, M., Madadkar-Sobhani, A., Mahnam, K., Fassihi, A., Saghaie, L., & Mansourian, M. (2011). Homology modeling of human CCR5 and analysis of its binding properties through molecular docking and molecular dynamics simulation. Biochimica et biophysica Acta, 1808(3), 802–817. https://doi.org/https://doi.org/10.1016/j.bbamem.2010.12.004
- Shebl, M. (2009). 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(19), 3217–3231. https://doi.org/https://doi.org/10.1080/00958970903012785
- Smith, B. C. (1998). Infrared spectral interpretation (1st ed.). CRC Press.
- Speier, G., Csihony, J., Whalen, A. M., & Pierpont, C. G. (1996). Studies on aerobic reactions of ammonia/3,5-di-tert-butylcatechol Schiff-base condensation products with Cu(I) and Cu(II). Strong Cu(II)-radical ferromagnetic exchange and observations on a unique N–N coupling reaction. Inorganic Chemistry, 35(12), 3519–3524. https://doi.org/https://doi.org/10.1021/ic950805l
- Spencer, E. A., Burns, C. S., Avdievich, N. I., Gerfen, G. J., Peisach, J., Antholine, W. E., Ball, H. L., Cohen, F. E., Prusiner, S. B., & Millhauser, G. L. (2000). Identification of the Cu2+ binding sites in the n-terminal domain of the prion protein by EPR and CD spectroscopy. Biochemistry, 39(45), 13760–13771. https://doi.org/https://doi.org/10.1021/bi001472t
- Spiro, T. G. (1980). Metal ion activation of dioxygen. Wiley.
- Stamos, J., Sliwkowski, M. X., & Eigenbrot, C. (2002). Structure of the epidermal growth factor receptor kinase domain alone and in complex with a 4-anilinoquinazoline inhibitor. The Journal of Biological Chemistry, 277(48), 46265–46272. https://doi.org/https://doi.org/10.1074/jbc.M207135200
- Szorcsik, A., Nagy, L., Sletten, J., Szalontai, G., Kamu, E., Fiore, T., Pellerito, L., & Kálmán, E. (2004). Preparation and structural studies on dibutyltin (IV) complexes with pyridine mono- and dicarboxylic acids. Journal of Organometallic Chemistry, 689(7), 1145–1154. https://doi.org/https://doi.org/10.1016/j.jorganchem.2003.11.040
- The PyMOL Molecular Graphics System. (2009). LLC, Schrodinger, Version 1.5.0.4.
- Uddin, N., Rashid, F., Ali, S., Tirmizi, S. A., Ahmad, I., Zaib, S., & Haider, A. (2020). Synthesis, characterization, and anticancer activity of Schiff bases. Journal of Biomolecular Structure and Dynamics, 38(11), 3246–3259.
- Wheate, N. J., Walker, S., Craig, G. E., & Oun, R. (2010). The status of platinum anticancer drugs in the clinic and in clinical trials. Dalton Transactions (Cambridge, England: 2003), 39(35), 8113–8127. https://doi.org/https://doi.org/10.1039/c0dt00292e