Density functional theory molecular modelling, DNA interactions, antioxidant, antimicrobial, anticancer and biothermodynamic studies of bioactive water soluble mixed ligand complexes

References

• Abo Dena, A. S. (2014). To the memory of Hugo Schiff: Applications of Schiff bases in potentiometric sensors. Russian Journal of Applied Chemistry, 87(3), 383–396. doi:10.1134/S1070427214030227
   Web of Science ®Google Scholar
• Abu-Surrah, A. S., & Kettunen, M. (2006). Platinum group antitumor chemistry: Design and development of new anticancer drugs complementary to cisplatin. Current Medicinal Chemistry, 13(11), 1337–1357. doi:10.2174/092986706776872970
   PubMed Web of Science ®Google Scholar
• Annaraj, B., Mitu, L., & Neelakantan, M. A. (2016). Synthesis and crystal structure of imidazole containing amide as a turn on fluorescent probe for nickel ion in aqueous media: An experimental and theoretical investigation. Journal of Molecular Structure, 1104, 1–6. doi:10.1016/j.molstruc.2015.10.002
   Web of Science ®Google Scholar
• Arnesano, F., & Natile, G. (2009). Mechanistic insight into the cellular uptake and processing of cisplatin 30 years after its approval by FDA. Coordination Chemistry Reviews, 253(15–16), 2070–2081. doi:10.1016/j.ccr.2009.01.028
   Web of Science ®Google Scholar
• Babu, M. S. S., Reddy, K. H., & Krishna, P. G. (2007). Synthesis, characterization, DNA interaction and cleavage activity of new mixed ligand copper(II) complexes with heterocyclic bases. Polyhedron, 26(3), 572–580. doi:10.1016/j.poly.2006.08.026
   Web of Science ®Google Scholar
• Benitez, J., Becco, L., Correia, I., Leal, S. M., Guiset, H., Pessoa, J. C., … Gambino, T. D. (2011). Vanadium polypyridyl compounds as potential antiparasitic and antitumoral agents: New achievements. Journal of Inorganic Biochemistry, 105(2), 303–312. doi:10.1016/j.jinorgbio.2010.11.001
   PubMed Web of Science ®Google Scholar
• Blasco, A. J., Gonzalez, M. C., & Escarpa, A. (2004). Electrochemical approach for discriminating and measuring predominant flavonoids and phenolic acids using differential pulse voltammetry: Towards an electrochemical index of natural antioxidants. Analytica Chimica Acta, 511(1), 71–81. doi:10.1016/j.aca.2004.01.038
   Web of Science ®Google Scholar
• Chandra, A., Samali, S., & Orrenius, S. (2000). Triggering and modulation of apoptosis by oxidative stress. Free Radical Biology and Medicine, 29(3–4), 323–333. doi:10.1016/S0891-5849(00)00302-6
   PubMed Web of Science ®Google Scholar
• Chanphai, P., & Tajmir-Riahi, H. A. (2017). DNA binding to folic acid-chitosan nanoconjugates. Journal of Biomolecular Structure and Dynamics, 1–6. doi:10.1080/07391102.2017.1371078
   PubMed Web of Science ®Google Scholar
• Chaires, J. B. (1997). Energetics of drug–DNA interactions. Biopolymers, 44(3), 201–215. doi:10.1002/(SICI)1097-0282(1997)44:3 < 201::AID-BIP2 > 3.0.CO;2-Z
   PubMed Web of Science ®Google Scholar
• Choi, C. W., Kim, S. C., Hwang, S. S., Choi, B. K., Ahn, H. J., Lee, M. Y., … Kim, S. K. (2002). Antioxidant activity and free radical scavenging capacity between Korean medicinal plants and flavonoids by assay-guided comparison. Plant Science, 163(6), 1161–1168. doi:10.1016/S0168-9452(02)00332-1
   Web of Science ®Google Scholar
• Das, U., Sakagami, H., Chu, Q., Wang, Q., Kawase, M., Selvakumar, P., … Dimmock, J. R. (2010). 3,5 Bis(benzylidene)-1-[4-2-(morpholin-4-yl)ethoxyphenylcarbonyl]-4-piperidone hydrochloride: A lead tumor-specific cytotoxin which induces apoptosis and autophagy. Bioorganic & Medicinal Chemistry Letters, 20(3), 912–917. doi:10.1016/j.bmcl.2009.12.076
   PubMed Web of Science ®Google Scholar
• Dhaveethu Raja, J., & Sakthikumar, K. (2015). Synthesis of water soluble transition metal(II) complexes from Morpholine condensed tridentate Schiff base: Structural elucidation, antimicrobial, antioxidant and DNA interaction studies. Journal of Chemical and Pharmaceutical Research, 7(10S), 23–34. Retrieved from http://www.jocpr.com/abstract/synthesis-of-water-soluble-transition-metalii-complexes-from-morpholine-condensed-tridentate-schiff-base-structural-eluc-7311.html
   Google Scholar
• Ebrahimipour, S. Y., Sheikhshoaie, I., Castro, J., Dusek, M., Tohidiyan, Z., Eigner, V., & Khaleghi, M. (2015). Synthesis, spectral characterization, structural studies, molecular docking and antimicrobial evaluation of new dioxidouranium(VI) complexes incorporating tetradentate N2O2 Schiff base ligands. RSC Advances, 5(115), 95104–95117. doi:10.1039/C5RA17524K
   Web of Science ®Google Scholar
• Fenton, H. J. H. (1894). LXXIII.—Oxidation of tartaric acid in presence of iron. Journal of the Chemical Society Transactions, 65(0), 899–910. doi:10.1039/CT8946500899
   Google Scholar
• Galindo-Murillo, R., & Cheatham, T. E. (2017). Computational DNA binding studies of (–)-epigallocatechin-3-gallate. Journal of Biomolecular Structure and Dynamics, 1–13. doi:10.1080/07391102.2017.1389306
   PubMedGoogle Scholar
• Gellert, M., Smith, C. E., Neville, D., & Felsenfeld, G. (1965). Actinomycin binding to DNA: Mechanism and specificity. Journal of Molecular Biology, 11(3), 445–457. doi:10.1016/S0022-2836(65)80001-8
   PubMed Web of Science ®Google Scholar
• Gubendran, A., Kumar, G. G. V., Kesavan, M. P., Rajagopal, G., Athappan, P., & Rajesh, J. (2018). New anthracene based Schiff base ligands appended Cu(II) complexes: Theoretical study, DNA binding and cleavage activities. Applied Organometallic Chemistry, 32(3), e4128. doi:10.1002/aoc.4128
   Web of Science ®Google Scholar
• Hirohama, T., Kuranuki, Y., Ebina, E., Sugizaki, T., Arii, H., Chikira, M., … Palaniandavar, M. (2005). Copper(II) complexes of 1,10-phenanthroline-derived ligands: Studies on DNA binding properties and nuclease activity. Journal of Inorganic Biochemistry, 99(5), 1205–1219. doi:10.1016/j.jinorgbio.2005.02.020
   PubMed Web of Science ®Google Scholar
• Javanmardi, J., Stushnoff, C., Locke, E., & Vivanco, J. M. (2003). Antioxidant activity and total phenolic content of Iranian Ocimum accessions. Food Chemistry, 83(4), 547–550. doi:10.1016/S0308-8146(03)00151-1
   Web of Science ®Google Scholar
• Karami, K., Mehri Lighvan, Z., Farrokhpour, H., Dehdashti Jahromi, M., & Momtazi-Borojeni, A. A. (2017). Synthesis and spectroscopic characterization study of new palladium complexes containing bioactive O,O-chelated ligands: Evaluation of the DNA/protein BSA interaction, in vitro antitumoural activity and molecular docking. Journal of Biomolecular Structure and Dynamics, 1–17. doi:10.1080/07391102.2017.1391125
   PubMed Web of Science ®Google Scholar
• Kesavan, M. P., Vinoth Kumar, G. G., Dhaveethu Raja, J., Anitha, K., Karthikeyan, S., & Rajesh, J. (2017). DNA interaction, antimicrobial, antioxidant and anticancer studies on Cu(II) complexes of Luotonin A. Journal of Photochemistry and Photobiology B: Biology, 167, 20–28. doi:10.1016/j.jphotobiol.2016.11.024
   PubMed Web of Science ®Google Scholar
• Khojasteh, R. R., & Matin, S. J. (2015). Synthesis, characterization and antibacterial activities of some metal complexes of heptadentate Schiff base ligand derived from acetylacetone. Russian Journal of Applied Chemistry, 88(6), 921–925. doi:10.1134/S107042721506004X
   Web of Science ®Google Scholar
• Khosravi, F., & Mansouri-Torshizi, H. (2018). Antibacterial combination therapy using Co3+, Cu2+, Zn2+ and Pd2+ complexes: Their calf thymus DNA binding studies. Journal of Biomolecular Structure and Dynamics, 36(2), 512–531. doi:10.1080/07391102.2017.1281171
   PubMed Web of Science ®Google Scholar
• Kosiha, A., Parthiban, C., Ciattini, S., Chelazzi, L., & Elango, K. P. (2017). Metal complexes of naphthoquinone based ligand: Synthesis, characterization, protein binding, DNA binding/cleavage and cytotoxicity studies. Journal of Biomolecular Structure and Dynamics, 1–12. doi: 10.1080/07391102.2017.1413423
   PubMed Web of Science ®Google Scholar
• Lakshmipraba, J., Arunachalam, S., Solomon, R. V., Venuvanalingam, P., Riyasdeen, A., Dhivya, R., & Akbarsha, M. A. (2015). Surfactant–copper(II) Schiff base complexes: Synthesis, structural investigation, DNA interaction, docking studies, and cytotoxic activity. Journal of Biomolecular Structure and Dynamics, 33(4), 877–891. doi:10.1080/07391102.2014.918523
   PubMed Web of Science ®Google Scholar
• Liu, W., Jiang, J., Xu, Y., Hou, S., Sun, L., Ye, Q., & Lou, L. (2015). Design, synthesis and anticancer activity of diam(m)ine platinum(II) complexes bearing a small-molecular cell apoptosis inducer dichloroacetate. Journal of Inorganic Biochemistry, 146, 14–18. doi:10.1016/j.jinorgbio.2015.02.002
   PubMed Web of Science ®Google Scholar
• Lozynskyi, A., Zimenkovsky, B., Radko, L., Stypula-Trebas, S., Roman, O., Gzella, A. K., & Lesyk, R. (2018). Synthesis and cytotoxicity of new thiazolo[4,5-b] pyridine-2(3H)-one derivatives based on α, β-unsaturated ketones and a-ketoacids. Chemical Papers, 72 (3), 669–681. doi:10.1007/s11696-017-0318-1
   Web of Science ®Google Scholar
• Maheswari, P. U., & Palaniandavar, M. (2004). DNA binding and cleavage properties of certain tetrammine ruthenium(II) complexes of modified 1,10-phenanthrolines – effect of hydrogen-bonding on DNA-binding affinity. Journal of Inorganic Biochemistry, 98(2), 219–230. doi:10.1016/j.jinorgbio.2003.09.003
   PubMed Web of Science ®Google Scholar
• Mathan Kumar, S., Kesavan, M. P., Vinoth Kumar, G. G., Sankarganesh, M., Chakkaravarthi, G., Rajagopal, G., & Rajesh, J. (2018). New heteroleptic Zn(II) complexes of thiosemicarbazone and diimine Co-Ligands: Structural analysis and their biological impacts. Journal of Molecular Structure, 1153, 1–11. doi:10.1016/j.molstruc.2017.09.070
   Web of Science ®Google Scholar
• Mohapatra, S. C., Tehlan, S., Hundal, M. S., & Mathur, P. (2008). Crystal structure and Catalytic activity of a copper(II) complex based on a tetradentate bis-benzimidazole diamide ligand. Inorganica Chimica Acta, 361(7), 1897–1907. doi:10.1016/j.ica.2007.10.002
   Web of Science ®Google Scholar
• Nagaraj, K., Murugan, K. S., Thangamuniyandi, P., & Sakthinathan, S. (2014). Nucleic acids binding study of surfactant copper(II) complex containing dipyrido[3,2-a:2′-3′-c] phenazine ligand as intercalator: In vitro antitumor activity of complex in human liver carcinoma (HepG2) Cancer Cells. RSC Advances, 4(99), 56084–56094. doi: 10.1039/C4RA08049A
   Web of Science ®Google Scholar
• Nimal Christhudas, I. V. S., Praveen Kumar, P., Sunil, C., Vajravijayan, S., Lakshmi Sundaram, R., Jenifer Siril, S., & Agastian, P. (2013). In vitro studies on a-glucosidase inhibition, antioxidant and free radical scavenging activities of Hedyotis biflora L. Food Chemistry, 138(2-3), 1689–1695. doi:10.1016/j.foodchem.2012.11.051
   PubMed Web of Science ®Google Scholar
• Nishikimi, M., Appaji Rao, N., & Yagi, K. (1972). The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochemical and Biophysical Research Communications, 46(2), 849–854. doi:10.1016/S0006-291X(72)80218-3
   PubMed Web of Science ®Google Scholar
• Oh, Y. S., Park, J. H., Han, S. W., Kim, S. K., & Lee, Y. A. (2017). Retained binding mode of various DNA-binding molecules under molecular crowding condition. Journal of Biomolecular Structure and Dynamics, 1–12. doi:10.1080/07391102.2017.1375992
   PubMed Web of Science ®Google Scholar
• Oyaizu, M. (1986). Studies on products of browning reactions: Antioxidative activities of products of browning reaction prepared from glucosamine. The Japanese Journal of Nutrition and Dietetics, 44(6), 307–315. doi:10.5264/eiyogakuzashi.44.307
   Google Scholar
• Parveen, S., & Sahoo, S. K. (2014). Corrigendum to ‘Long circulating chitosan/PEG blended PLGA nanoparticle for tumor drug delivery’ [Eur. J. Pharmacol. 670 (2–3), 372–383]. European Journal of Pharmacology, 727, 186. doi:10.1016/j.ejphar.2014.02.009
   Google Scholar
• Parveen, S., & Arjmand, F. (2012). De novo design, synthesis and spectroscopic characterization of chiral benzimidazole-derived amino acid Zn(II) complexes: Development of tryptophan-derived specific hydrolytic DNA artificial nuclease agent. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 85(1), 53–60. doi:10.1016/j.saa.2011.09.006
   PubMed Web of Science ®Google Scholar
• Patel, A., Patel, A., Patel, A., & Patel, N. M. (2010). Determination of polyphenols and free radical scavenging activity of tephrosia purpurea linn leaves (Leguminosae). Pharmacognosy Research, 2(3), 152–158. doi:10.4103/0974-8490.65509
   PubMedGoogle Scholar
• Patra, D., Paul, S., Sepay, N., Kundu, R., & Ghosh, T. (2017). Structure-activity relationship on DNA binding and anticancer activities of a family of mixed-ligand oxidovanadium(V) hydrazone complexes. Journal of Biomolecular Structure and Dynamics, 1–13. doi:10.1080/07391102.2017.1409652
   PubMed Web of Science ®Google Scholar
• Patra, A. K., Nethaji, M., & Chakravarty, A. R. (2007). Synthesis, crystal structure, DNA binding and photo-induced DNA cleavage activity of (S-methyl-L-cysteine)copper(II) complexes of heterocyclic bases. Journal of Inorganic Biochemistry, 101(2), 233–244. doi:10.1016/j.jinorgbio.2006.09.018
   PubMed Web of Science ®Google Scholar
• Petrovic, Z. D., Dorovic, J., Simijonović, D., Trifunovic, S., & Petrovic, V. P. (2018). In vitro study of iron coordination properties, anti‑inflammatory potential and cytotoxic effects of N‑salicylidene and N‑vanillidene anil Schiff bases. Chemical Papers, 72, 2171–2180. doi:10.1007/s11696-018-0419-5
   Web of Science ®Google Scholar
• Rabindra Reddy, P., Shilpa, A., Raju, N., & Raghavaiah, P. (2011). Synthesis, structure, DNA binding and cleavage properties of ternary amino acid Schiff base-phen/bipy Cu(II) complexes. Journal of Inorganic Biochemistry, 105(12), 1603–1612. doi:10.1016/j.jinorgbio.2011.08.022
   PubMed Web of Science ®Google Scholar
• Raja, A., Rajendiran, V., Maheswari, P. U., Balamurugan, R., Kilner, C. A., M. A., Halcrow., & Palaniandavar, M. (2005). Copper(II) complexes of tridentate pyridylmethylethylenediamines: Role of ligand steric hindrance on DNA binding and cleavage. Journal of Inorganic Biochemistry, 99(8), 1717–1732. doi:10.1016/j.jinorgbio.2005.05.014
   PubMed Web of Science ®Google Scholar
• Rajendran, V., Karthick, R., Palaniandavar, M., Stoeckli-Evans, H., Periyasamy, V. S., Akbarsha, M. A., … Krishnamoorthy, H. (2007). Mixed-ligand copper(II)-phenolate complexes: Effect of coligand on enhanced DNA and protein binding, DNA cleavage and anticancer activity. Inorganic Chemistry, 46(20), 8208–8221. doi:10.1021/ic700755p
   PubMed Web of Science ®Google Scholar
• Rajesh, J., Kesavan, M. P., Ayyanaar, S., Karthikeyan, K., Rajagopal, G., & Athappan, P. (2017). DNA interaction and cleavage studies of ancillary chiral ligand and N, N-donor ligands coordinated platinum(II) complexes. Applied Organometallic Chemistry, 31(12), e3868. doi:10.1002/aoc.3868
   Web of Science ®Google Scholar
• Ramakrishnan, S., Rajendiran, V., Palaniandavar, M., Periasamy, V. S., Srinag, B. S., Krishnamurthy, H., & Akbarsha, M. A. (2009). Induction of cell death by ternary copper(II) complexes of l-tyrosine and diimines: Role of coligands on DNA binding and cleavage and anticancer activity. Inorganic Chemistry, 48(4), 1309–1322. doi:10.1021/ic801144x
   PubMed Web of Science ®Google Scholar
• Raman, N., & Pravin, N. (2014). DNA fastening and ripping actions of novel Knoevenagel condensed dicarboxylic acid complexes in antitumor journey. European Journal of Medicinal Chemistry, 80, 57–70. doi:10.1016/j.ejmech.2014.04.032
   PubMed Web of Science ®Google Scholar
• Raman, N., Jeyamurugan, R., Subbulakshmi, M., Boominathan, R., & Yuvarajan, C. R. (2010). Synthesis, DNA binding and antimicrobial studies of novel metal complexes containing a pyrazolone derivative Schiff base. Chemical Papers, 64 (3), 318–328. doi: 10.2478/s11696-010-0003-0
   Web of Science ®Google Scholar
• Raman, N., S., Ali, S., D., & Raja, J. (2008). Designing, synthesis and spectral characterization of Schiff base transition metal complexes: DNA cleavage and antimicrobial activity studies. Journal of the Serbian Chemical Society, 73(11), 1063–1071. doi: 10.2298/JSC0811063R
   Web of Science ®Google Scholar
• Raman, N., Dhaveethu Raja, J., & Sakthivel, A. (2007). Synthesis, spectral characterization of Schiff base transition metal complexes: DNA cleavage and antimicrobial activity studies. Journal of Chemical Sciences, 119(4), 303–310. doi:10.1007/s12039-007-0041-5
   Web of Science ®Google Scholar
• Record, M. T., Anderson, C. F., & Lohman, T. M. (1978). Thermodynamic analysis of ion effects on the binding and conformational equilibria of proteins and nucleic acids: The roles of ion association or release, screening, and ion effects on water activity. Quarterly Reviews of Biophysics, 11(02), 103–178. doi:10.1017/S003358350000202X
   PubMedGoogle Scholar
• Reddy, K. P., Subhani, S. M., Khan, P. A., & Kumar, K. B. (1985). Effect of light and benzyladenine on dark-treated growing rice (Oryza sativa) leaves II. changes in peroxidase activity. Plant and Cell Physiology, 26(6), 987–994. doi:10.1093/oxfordjournals.pcp.a077018
   Web of Science ®Google Scholar
• Revathi, N., Sankarganesh, M., Rajesh, J., & Raja, J. D. (2017). Biologically active Cu(II), Co(II), Ni(II) and Zn(II) complexes of pyrimidine derivative schiff base: DNA binding, antioxidant, antibacterial and in vitro anticancer studies. Journal of Fluorescence, 27(5), 1801–1814. doi:10.1007/s10895-017-2118-y
   PubMed Web of Science ®Google Scholar
• Sankarganesh, M., Rajesh, J., Vinoth Kumar, G. G., Vadivel, M., Mitu, L., Senthil Kumar, R., & Dhaveethu Raja, J. (2018). Spectral characterization, theoretical, antimicrobial, DNA interaction and in vitro anticancer studies of Cu(II) and Zn(II) complexes with pyrimidine-morpholine based Schiff base ligand. Journal of Saudi Chemical Society, 22(4), 416–426. doi:10.1016/j.jscs.2017.08.007
   Web of Science ®Google Scholar
• Sankarganesh, M., Adwin Jose, P., Dhaveethu Raja, J., Kesavan, M. P., Vadivel, M., Rajesh, J., … Karthikeyan, S. (2017). New pyrimidine based ligand capped gold and platinum nano particles: Synthesis, characterization, antimicrobial, antioxidant, DNA interaction and in vitro anticancer activities. Journal of Photochemistry and Photobiology B: Biology, 176, 44–53. doi:10.1007/s10895-017-2118-y
   PubMed Web of Science ®Google Scholar
• Santini, C., Pellei, M., Gandin, V., Porchia, M., Tisato, F., & Marzano, C. (2014). Advances in copper complexes as anticancer agents. Chemical Reviews, 114(1), 815–862. doi: 10.1021/cr400135x
   PubMed Web of Science ®Google Scholar
• Selvaganapathy, M., & Raman, N. (2016). Pharmacological activity of a few transition metalcomplexes: A short review. Journal of Chemical Biology & Therapeutics, 01(02). doi: 10.4172/2572-0406.1000108
   Google Scholar
• Selwin Joseyphus, R. S., & Sivasankaran Nair, M. (2010). Synthesis, characterization and biological studies of some Co(II), Ni(II) and Cu(II) complexes derived from indole-3-carboxaldehyde and glycylglycine as Schiff base ligand. Arabian Journal of Chemistry, 3(4), 195–204. doi:10.1016/j.arabjc.2010.05.001
   Web of Science ®Google Scholar
• Shahabadi, N., Fatahi, N., Mahdavi, M., Nejad, Z. K., & Pourfoulad, M. (2011). Multispectroscopic studies of the interaction of calf thymus DNA with the anti-viral drug, valacyclovir. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 83(1), 420–424. doi:10.1016/j.saa.2011.08.056
   PubMed Web of Science ®Google Scholar
• Shamel, A., & Salemnoush, T. (2016). Synthesis and fluorescence study of the grafted salicylidene Schiff base onto SBA-15 mesoporous silica for detecting Zn2+ traces in aqueous medium. Russian Journal of Applied Chemistry, 89(3), 500–504. doi:10.1134/S10704272160030228
   Web of Science ®Google Scholar
• Shanmugapriya, A., Jain, R., Sabarinathan, D., Kalaiarasi, G., Dallemer, F., & Prabhakaran, R. (2017). Structurally different mono-, bi- and trinuclear Pd(II) complexes and their DNA/protein interaction, DNA cleavage, and anti-oxidant, anti-microbial and cytotoxic studies. New Journal of Chemistry, 41(18), 10324–10338. doi: 10.1039/C7NJ01556A
   Web of Science ®Google Scholar
• Shujah, S., Khalid, N., & Ali, S. (2017). Homobimetallic organotin(IV) complexes with succinohydrazide Schiff base: Synthesis, spectroscopic characterization and biological screening. Russian Journal of General Chemistry, 87(3), 515–522. doi:10.1134/S1070363217030227
   Web of Science ®Google Scholar
• Singh, P., Khare, D., & Pande, R. (2014). Evaluation of antioxidant activity and DNA cleavage protection effect of naphthyl hydroxamic acid derivatives through conventional and fluorescence microscopic methods. Chemical Papers, 68(10), 1298–1304. doi:10.2478/s11696-014-0576-0
   Web of Science ®Google Scholar
• Solomon, R. V., Jagadeesan, R., Vedha, S. A., & Venuvanalingam, P. (2014). A DFT/TDDFT modelling of bithiophene azo chromophores for optoelectronic applications. Dyes and Pigments, 100, 261–268. doi:10.1016/j.dyepig.2013.09.016
   Web of Science ®Google Scholar
• Solomon, R. V., Veerapandian, P., Vedha, S. A., & Venuvanalingam, P. (2012). Tuning nonlinear optical and optoelectronic properties of vinyl coupled triazene chromophores: A density functional theory and time-dependent density functional theory investigation. The Journal of Physical Chemistry A, 116(18), 4667–4677. doi:10.1021/jp302276w
   PubMed Web of Science ®Google Scholar
• Solomon, R. V., Bella, A. P., Vedha, S. A., & Venuvanalingam, P. (2012). Designing benzosiloles for better optoelectronic properties using DFT & TDDFT approaches. Physical Chemistry Chemical Physics, 14(41), 14229–14237. doi:10.1039/C2CP41554B
   PubMed Web of Science ®Google Scholar
• Sukkur Saleem, S. H., Sankarganesh, M., Adwin Jose, P., Sakthikumar, K., Mitu, L., & Dhaveethu Raja, J. (2017). Investigation of antimicrobial, antioxidant, and DNA binding studies of bioactive Cu(II), Zn(II), Co(II), and Ni(II) Complexes of pyrimidine derivative schiff base ligand. Journal of Chemistry, 2017, 1–8. doi:10.1155/2017/3831507
   Web of Science ®Google Scholar
• Thimmaiah, K. N., Lloyd, W. D., & Chandrappa, G. T. (1985). Stereochemistry and fungitoxicity of complexes of p-anisaldehydethiosemicarbazone with Mn(II), Fe(II), Co(II) and Ni(II). Inorganica Chimica Acta, 106(2), 81–83. doi:10.1016/S0020-1693(00)82252-5
   Web of Science ®Google Scholar
• Van Acker, S. A. B. E., Koymans, L. M. H., & Bast, A. (1993). Molecular pharmacology of vitamin E: Structural aspects of antioxidant activity. Free Radical Biology and Medicine, 15(3), 311–328. doi:10.1016/0891-5849(93)90078-9
   PubMed Web of Science ®Google Scholar
• Xu, Y., Zhang, H., Shen, K., Mao, S., Shi, X., & Wu, H. (2018). Four- five- and six-coordinated transition metal complexes based on naphthalimide Schiff base ligands: Synthesis, crystal structure and properties. Applied Organometallic Chemistry, 32(1), e3902–e3913. doi:10.1002/aoc.3902
   Web of Science ®Google Scholar
• Zhao, F., Wang, W., Lu, W., Xu, L., Yang, S., Cai, X. M., … Cao, F. (2018). High anticancer potency on tumor cells of dehydroabietylamine Schiff-base derivatives and a copper(II) complex. European Journal of Medicinal Chemistry, 146, 451–459. doi:10.1016/j.ejmech.2018.01.041
   PubMed Web of Science ®Google Scholar
• Zhou, X., Zhang, C., Zhang, G., & Liao, Y. (2016). Intercalation of daphnetin–Cu(II) complex with calf thymus DNA. RSC Advances, 6(7), 5408–5418. doi:10.1039/C5RA22274E
   Web of Science ®Google Scholar