How to cite this paper
Sharma, D & Revanasiddappa, H. (2019). Synthesis, spectroscopic characterization, crystal structure and Hirshfeld surface analysis of Co(III), Ni(II) and VO(IV) metal complexes with a novel Schiff base ligand and their antimicrobial activities.Current Chemistry Letters, 8(1), 39-52.
Refrences
1. Isloor A. M., Kalluraya B., and Shetty P. (2009) Regioselective reaction: synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles. Eur. J. Med. Chem. 44 (9) 3784–7.
2. Mohareb R. M., El-Sayed N. N. E. and Abdelaziz M. A. (2012) Uses of Cyanoacetylhydrazine in Heterocyclic Synthesis: Novel Synthesis of Pyrazole Derivatives with Anti-tumor Activities. Molecules 17 (7) 8449–63.
3. Ziegler J., Schuerle T., Pasierb L., Kelly C., Elamin A., Cole K. A., and Wright D. W. (2000) The Propionate of Heme Binds N4O2 Schiff Base Antimalarial Drug Complexes. Inorg. Chem. 39 (16) 3731–3733.
4. Annapoorani S., and Krishnan C. N. (2013) Synthesis And Spectroscopic Studies Of Trinuclear N4 Schiff Base Complexess, J. Chem. Tech. Res. 5 (1) 180-185.
5. Shoaib K., Rehman W., Mohammad B. and Ali S. (2013) Synthesis, Characterization and Biological Applications of Transition Metal Complexes of [no] Donor Schiff Bases. J. Proteomics Bioinform. 6 (7) 153–7.
6. Chang H. Q., Jia L., Xu J., Zhu T. F., Xu Z. Q., and Chen R. H. (2016) Syntheses, crystal structures, anticancer activities of three reduce Schiff base ligand based transition metal complexes. J. Mol. Struct. 1106, 366–72.
7. Khamamkar A. and Pallapothula V. R. (2014) Synthesis and charecterisation of complexes derived from succinyl dihydrazide and 3-acetyl-6- methyl-2H-pyran-2, 4(3H)-dione. Acta Biomed. Sci. 1 (4) 179-184.
8. Temel H., and Sekerci M., (2001) Novel complexes of manganese(iii), cobalt(ii), copper(II), and zinc(II) with Schiff base derived from 1,2-bis(p-amino-phenoxy)ethane and salicylaldehyde. Synth. React. Inorg. Met. Org. Chem. 31 (5) 849-57.
9. Watanabe K., Ohta T., and Shirasu Y. (1989) Enhancement and inhibition of mutation by o-vanillin in Escherichia coli. Mutat. Res.218 (2) 105-9.
10. Pelgrift R. Y., and Friedman A. J. (2013) Nanotechnology as a therapeutic tool to combat microbial resistance. Adv. Drug Deliv. Rev. 65 (13–14) 21803–1815.
11. Boyd D. B. (1983) Substituent effects in cephalosporins as assessed by molecular orbital calculations, nuclear magnetic resonance, and kinetics. J. Med. Chem. 26 (7) 1010-1013.
12. Spackman M. A., and McKinnon J. J. (2002) Fingerprinting intermolecular interactions in molecular crystals. CrystEng Comm. 4 (66) 378–392.
13. Soman R., Sujatha S., Sushmita De., Rojisha V.C., Parameswaran P., Varghese B., and Arunkumar C. (2014) Intermolecular Interactions in Fluorinated Tetraarylporphyrins: An Experimental and Theoretical Study. Eur. J. Inorg. Chem. 2014 (16) 2653–2662.
14. Kumar L. S., Prasad K. S., and Revanasiddappa H. D. (2013) SODs, DNA binding and cleavage studies of new Mn(III) complexes with 2-((3-(benzyloxy)pyridin-2-ylimino)methyl)phenol. Spectrochim Acta A Mol Biomol Spectrosc. 107, 203–212.
15. Ma J-X., Li Q-L., Li P-P., Zhao J-X., and Zhao L. (2018) Crystal structure of bis{5-methoxy-2-((E)-((4-((E)-1-(methoxyimino)ethyl)phenyl)imino)methyl)phenolato-κ 2N,O}nickel(II), C34H34N4NiO6. Z. Kristallogr. - New Cryst. Struct. 233 (5) 767-769.
16. Hong Y., Liu W., and Gou G. (2018) Crystal structure of [4-chloro-2-(((2-((3-ethoxy-2-oxidobenzylidene)amino)phenyl)imino)(phenyl)methyl)phenolato-κ4N,N′,O,O′}nickel(II) - ethyl acetate (1/1), C32H29ClN2NiO5. Z. Kristallogr. - New Cryst. Struct. 233 (6) 989-991.
17. Neelakantan M. A., Rusalraj F., Dharmaraja J., Johnsonraja S., Jeyakumar T., and Pillai M.S. (2008) Spectral characterization, cyclic voltammetry, morphology, biological activities and DNA cleaving studies of amino acid Schiff base metal(II) complexes. Spectrochim. Acta Part A 71(4) 1599-1609.
18. Gull P., AL-Thabaiti S.A., and Hashmi A.A. (2014) Design, Characterization and antimicrobial activity of Cu(II), Co(II) and Zn(II) complexes with Schiff base from 1,2-diphenylethane-1,2-dione and N-(1-Naphthyl) ethylenediamine. Int. J. Multidiscip. Curr. Res. 2 (6) 1142-1147.
19. Kumar S., Deepak V., Kumari M., and Dutta P.K. (2015) Antibacterial activity of diisocyanate-modified chitosan for biomedical applications. Int. J. Bio. Macro. 84, 349-353.
20. Raman N., Ravichandran S., and Thangaraja C. (2004) Copper(II), cobalt(II), nickel(II) and zinc(II) complexes of Schiff base derived from benzil-2,4-dinitrophenylhydrazone with aniline. J. Chem. Sci.116 (4) 215-219.
21. Pranita U.G., Mandlik P.R., and Aswar A.S. (2015) Synthesis and characterization of Cr(III), Mn(III), Fe(III), VO(IV), Zr(IV) and UO2 (VI) complexes of schiff base derived from isonicotinoylhydrazine. Indian J. Pharm. Sci. 77 (4) 376-381.
22. Prasad K. S., Kumar L. S., Shekar S. C., Prasad M., and Revanasiddappa H. D. (2011) Oxovanadium Complexes with Bidentate N, O Ligands: Synthesis, Characterization, DNA Binding, Nuclease Activity and Antimicrobial Studies. Chem. Sci. J. 2 (1) 1-10.
23. Belaid S., Landreau A., Djebbar S., Benali-Baitich O., Bouet G., and Bouchara J. P. (2008) Synthesis, characterization and antifungal activity of a series of manganese(II) and copper(II) complexes with ligands derived from reduced N,N′-O-phenylenebis(salicylideneimine). J. Inorg.Biochem. 102 (1) 63–69.
24. El-Sherif A. A., Shoukry M. M., and Abd-Elgawad M. M. A. (2012) Synthesis, characterization, biological activity and equilibrium studies of metal(II) ion complexes with tridentate hydrazone ligand derived from hydralazine. Spectrochim. Acta A Mol. Biomol. Spectrosc. 98, 307-321
25. Dharamaraj N., Viswanathamurthi P., and Natarajan K. (2001) Ruthenium(II) complexes containing bidentate Schiff bases and their antifungal activity. Tran. Met. Chem. 26 (1-2) 105–109.
26. Tweedy B.G. (1964) Plant extracts with metal ions as potential antimicrobial agents. Phytopathology 55, 910-914.
27. Takjoo R., Akbari A., Ebrahimipour S.Y., Kubicki M., Mohamadi M., and Mollania N. (2017) Synthesis, spectral characterization, DFT calculations, antimicrobial activity and molecular docking of 4-bromo-2-((2-hydroxy-5-methylphenylimino)methyl)phenol and its V(V) complex. Inorg. Chim. Acta 455 (1) 173–182.
28. Sheldrick G. M. (2008) A short history of SHELX. Acta cryst. A 64. 112-122.
29. Sheldrick G. M. (2015) Crystal structure refinement with SHELXL. Acta cryst. C 71 3-8.
2. Mohareb R. M., El-Sayed N. N. E. and Abdelaziz M. A. (2012) Uses of Cyanoacetylhydrazine in Heterocyclic Synthesis: Novel Synthesis of Pyrazole Derivatives with Anti-tumor Activities. Molecules 17 (7) 8449–63.
3. Ziegler J., Schuerle T., Pasierb L., Kelly C., Elamin A., Cole K. A., and Wright D. W. (2000) The Propionate of Heme Binds N4O2 Schiff Base Antimalarial Drug Complexes. Inorg. Chem. 39 (16) 3731–3733.
4. Annapoorani S., and Krishnan C. N. (2013) Synthesis And Spectroscopic Studies Of Trinuclear N4 Schiff Base Complexess, J. Chem. Tech. Res. 5 (1) 180-185.
5. Shoaib K., Rehman W., Mohammad B. and Ali S. (2013) Synthesis, Characterization and Biological Applications of Transition Metal Complexes of [no] Donor Schiff Bases. J. Proteomics Bioinform. 6 (7) 153–7.
6. Chang H. Q., Jia L., Xu J., Zhu T. F., Xu Z. Q., and Chen R. H. (2016) Syntheses, crystal structures, anticancer activities of three reduce Schiff base ligand based transition metal complexes. J. Mol. Struct. 1106, 366–72.
7. Khamamkar A. and Pallapothula V. R. (2014) Synthesis and charecterisation of complexes derived from succinyl dihydrazide and 3-acetyl-6- methyl-2H-pyran-2, 4(3H)-dione. Acta Biomed. Sci. 1 (4) 179-184.
8. Temel H., and Sekerci M., (2001) Novel complexes of manganese(iii), cobalt(ii), copper(II), and zinc(II) with Schiff base derived from 1,2-bis(p-amino-phenoxy)ethane and salicylaldehyde. Synth. React. Inorg. Met. Org. Chem. 31 (5) 849-57.
9. Watanabe K., Ohta T., and Shirasu Y. (1989) Enhancement and inhibition of mutation by o-vanillin in Escherichia coli. Mutat. Res.218 (2) 105-9.
10. Pelgrift R. Y., and Friedman A. J. (2013) Nanotechnology as a therapeutic tool to combat microbial resistance. Adv. Drug Deliv. Rev. 65 (13–14) 21803–1815.
11. Boyd D. B. (1983) Substituent effects in cephalosporins as assessed by molecular orbital calculations, nuclear magnetic resonance, and kinetics. J. Med. Chem. 26 (7) 1010-1013.
12. Spackman M. A., and McKinnon J. J. (2002) Fingerprinting intermolecular interactions in molecular crystals. CrystEng Comm. 4 (66) 378–392.
13. Soman R., Sujatha S., Sushmita De., Rojisha V.C., Parameswaran P., Varghese B., and Arunkumar C. (2014) Intermolecular Interactions in Fluorinated Tetraarylporphyrins: An Experimental and Theoretical Study. Eur. J. Inorg. Chem. 2014 (16) 2653–2662.
14. Kumar L. S., Prasad K. S., and Revanasiddappa H. D. (2013) SODs, DNA binding and cleavage studies of new Mn(III) complexes with 2-((3-(benzyloxy)pyridin-2-ylimino)methyl)phenol. Spectrochim Acta A Mol Biomol Spectrosc. 107, 203–212.
15. Ma J-X., Li Q-L., Li P-P., Zhao J-X., and Zhao L. (2018) Crystal structure of bis{5-methoxy-2-((E)-((4-((E)-1-(methoxyimino)ethyl)phenyl)imino)methyl)phenolato-κ 2N,O}nickel(II), C34H34N4NiO6. Z. Kristallogr. - New Cryst. Struct. 233 (5) 767-769.
16. Hong Y., Liu W., and Gou G. (2018) Crystal structure of [4-chloro-2-(((2-((3-ethoxy-2-oxidobenzylidene)amino)phenyl)imino)(phenyl)methyl)phenolato-κ4N,N′,O,O′}nickel(II) - ethyl acetate (1/1), C32H29ClN2NiO5. Z. Kristallogr. - New Cryst. Struct. 233 (6) 989-991.
17. Neelakantan M. A., Rusalraj F., Dharmaraja J., Johnsonraja S., Jeyakumar T., and Pillai M.S. (2008) Spectral characterization, cyclic voltammetry, morphology, biological activities and DNA cleaving studies of amino acid Schiff base metal(II) complexes. Spectrochim. Acta Part A 71(4) 1599-1609.
18. Gull P., AL-Thabaiti S.A., and Hashmi A.A. (2014) Design, Characterization and antimicrobial activity of Cu(II), Co(II) and Zn(II) complexes with Schiff base from 1,2-diphenylethane-1,2-dione and N-(1-Naphthyl) ethylenediamine. Int. J. Multidiscip. Curr. Res. 2 (6) 1142-1147.
19. Kumar S., Deepak V., Kumari M., and Dutta P.K. (2015) Antibacterial activity of diisocyanate-modified chitosan for biomedical applications. Int. J. Bio. Macro. 84, 349-353.
20. Raman N., Ravichandran S., and Thangaraja C. (2004) Copper(II), cobalt(II), nickel(II) and zinc(II) complexes of Schiff base derived from benzil-2,4-dinitrophenylhydrazone with aniline. J. Chem. Sci.116 (4) 215-219.
21. Pranita U.G., Mandlik P.R., and Aswar A.S. (2015) Synthesis and characterization of Cr(III), Mn(III), Fe(III), VO(IV), Zr(IV) and UO2 (VI) complexes of schiff base derived from isonicotinoylhydrazine. Indian J. Pharm. Sci. 77 (4) 376-381.
22. Prasad K. S., Kumar L. S., Shekar S. C., Prasad M., and Revanasiddappa H. D. (2011) Oxovanadium Complexes with Bidentate N, O Ligands: Synthesis, Characterization, DNA Binding, Nuclease Activity and Antimicrobial Studies. Chem. Sci. J. 2 (1) 1-10.
23. Belaid S., Landreau A., Djebbar S., Benali-Baitich O., Bouet G., and Bouchara J. P. (2008) Synthesis, characterization and antifungal activity of a series of manganese(II) and copper(II) complexes with ligands derived from reduced N,N′-O-phenylenebis(salicylideneimine). J. Inorg.Biochem. 102 (1) 63–69.
24. El-Sherif A. A., Shoukry M. M., and Abd-Elgawad M. M. A. (2012) Synthesis, characterization, biological activity and equilibrium studies of metal(II) ion complexes with tridentate hydrazone ligand derived from hydralazine. Spectrochim. Acta A Mol. Biomol. Spectrosc. 98, 307-321
25. Dharamaraj N., Viswanathamurthi P., and Natarajan K. (2001) Ruthenium(II) complexes containing bidentate Schiff bases and their antifungal activity. Tran. Met. Chem. 26 (1-2) 105–109.
26. Tweedy B.G. (1964) Plant extracts with metal ions as potential antimicrobial agents. Phytopathology 55, 910-914.
27. Takjoo R., Akbari A., Ebrahimipour S.Y., Kubicki M., Mohamadi M., and Mollania N. (2017) Synthesis, spectral characterization, DFT calculations, antimicrobial activity and molecular docking of 4-bromo-2-((2-hydroxy-5-methylphenylimino)methyl)phenol and its V(V) complex. Inorg. Chim. Acta 455 (1) 173–182.
28. Sheldrick G. M. (2008) A short history of SHELX. Acta cryst. A 64. 112-122.
29. Sheldrick G. M. (2015) Crystal structure refinement with SHELXL. Acta cryst. C 71 3-8.