Study on molecular structure, Spectral investigations, NBO, NLO, Hirshfeld surface analysis and Homo-Lumo energy of silver complex of 4-Amino-N-(2,6-dimethoxypyrimidin-4-yl)benzenesulfonamide

References

• Torrea, M. H.; Facchina, G.; Kremera, E.; Castellanob, E. E.; Piroc, O. E.; Baran, E. J. Characterization. J. Inorg. Biochem. 2003, 94, 200–204.
   Web of Science ®Google Scholar
• Supuran, C. T. Carbonic anhydrase inhibitors-syntheses, properties and physiological significance. Roum. Chem. Q. Rev. 1993, 1, 77–116.
   Google Scholar
• Supuran, C. T.; Scozzafava, A.; Saramet, I.; Banciu, M. D. Carbonic Anhydrase inhibitors: Inhibition of Isozymes I, II and IV with Heterocyclic Mercaptans, Sulfenamides, Sulfonamides and their Metal Complexes. J. Enzyme Inhib. 1998, 13(3), 177–194.
   Google Scholar
• Scozzafava, A.; Owa, T.; Mastrolorenzo, A.; Supuran, C. T. Anticancer and Antiviral Sulfonamides. Curr. Med. Chem. 2003, 10(11), 925–953. https://doi.org/10.2174/0929867033457647
   Web of Science ®Google Scholar
• Supuran, C. T.; Scozzafava, A. Carbonic anhydrase inhibitors, Med. Res. Rev. 2003, 23(2), 146–189. https://doi.org/10.1002/med.10025
   Web of Science ®Google Scholar
• Supuran, C. T. Indisulam: an anticancer sulfonamide in clinical development. Expert Opin. Invest. Drugs. 2003, 12(2), 283–287.
   Web of Science ®Google Scholar
• Cook, D. S.; Turner, M. F. Crystal and molecular structure of silver sulphadiazine (N1-pyrimidin-2-ylsulphanilamide). J. Chem. Soc. Perkin Trans. 1975, 2, 1021. https://doi.org/10.1039/p29750001021
   Google Scholar
• Brown, C. J.; Cook, D. S.; Sengier, L. Acta Cryst. 1985, C41, 718.
   Google Scholar
• Ochieng, J.; Platt, D.; Tait, L.; Hogan, V.; Raz, T.; Carmi, P.; Raz, A. Biochemistry. 1993, 32(16), 4455–4460. https://doi.org/10.1021/bi00067a038
   Web of Science ®Google Scholar
• De Clercq, E.; Holy, A. J. Med. Chem. 1979, 22(5), 510–513. https://doi.org/10.1021/jm00191a010
   Web of Science ®Google Scholar
• Chicheportiche, R.; Vincent, J. P.; Kopeyan, C.; Schweitz, H.; Lazdunski, M. Biochemistry. 1975, 14(10), 2081–2091. https://doi.org/10.1021/bi00681a007
   Web of Science ®Google Scholar
• Lewis, R. A. Chapter 4: The Development of Molecular Modeling Programs: The Use and Limitations of Physical Models. In Drug Design Strategies: Quantitative Approaches. Royal Society of Chemistry; Gramatica P., Livingstone D. J., Davis A. M., Eds., 2011; pp 88–107.
   Google Scholar
• Rajamani, R.; Good, A. C. Curr. Opin. Drug Discovery Dev. 2007, 10(3), 308–15.
   Google Scholar
• Panini, P.; Mohan, T. P.; Gangwar, U.; Sankollid, R.; Chopra, D. CrystEngComm. 2013, 15, 45–49.
   Google Scholar
• Farrugia, L. J. WinGX Program System. J. Appl. Crystallogr. 2012, 45, 849. https://doi.org/10.1107/S0021889812029111
   Web of Science ®Google Scholar
• Sheldrick, G. M. SHELXS-86 Program for the Solution of Crystal Structures; University of Gottingen: Gottingen, Germany, 2008.
   Google Scholar
• Spek, A. L. PLATON, University of Utrecht, Netherlands. Acta Crystallogr. 2005, A46, 194.
   Google Scholar
• Farrugia, L. J. Ortep-3 for Windows. J. Appl. Crystallogr. 2013, 45, 849. https://doi.org/10.1107/S0021889812029111
   Web of Science ®Google Scholar
• Bochevarov, A. D.; Harder, E.; Hughes, T. F.; Greenwood, J. R.; Braden, D. A.; Philipp, D. M.; Rinaldo, D.; Halls, M. D.; Zhang, J.; Friesner, R. A. Int. J. Quantum Chem. 2013, 113, 2110. https://doi.org/10.1002/qua.24481
   Web of Science ®Google Scholar
• Wolff, K.; Grimwood, D. J.; McKinnon, J. J.; Turner, M. J.; Jayatilaka, D.; Spackman, M. A. Crystal Explorer ver. 3.1; University of Western Australia: Perth, 2013.
   Google Scholar
• Lin-Vien, D.; Colthup, N. B.; Fately, W. G.; Grasselli, J. G. The Handbook of Infrared and Raman Characteristic Frequencies of Organic Molecules; Academic Press: San Diego, 1991.
   Google Scholar
• Nakamoto, K. Infrared and Raman Spectra of Inorganic and Coordination Compounds; John Wiley & Sons: USA, 1997.
   Google Scholar
• Kanagaraj, G.; Rao, G. N. Synth. React. Inorg. Met.-Org. Chem. 1992, 22, 559. https://doi.org/10.1080/15533179208020229
   Web of Science ®Google Scholar
• Tella, A. D.; Obaleye, J. A. Bull. Chem. Soc. Ethiop. 2011, 25, 371. https://doi.org/10.4314/bcse.v25i3.68589
   Web of Science ®Google Scholar
• Tailor, S. M.; Patel, U. H. 2017, 47(2).
   Google Scholar
• Kanagaraj, G.; Rao, G. N. Synth. React. Inorg. Met.-Org. Chem. 1992, 22, 5. https://doi.org/10.1080/15533179208020229
   Google Scholar
• Venugopala Reddy, K. R.; Keshavayya, J.; Seetharamappa, J. Dyes Pigm. 2003, 59,237. https://doi.org/10.1016/S0143-7208(03)00114-1
   Web of Science ®Google Scholar
• Broido, A. J. Polymer Sci. 1969, 7, 1761.
   Web of Science ®Google Scholar
• Coats, A. W.; Redfern, J. P. Nature. 1964, 201, 68. https://doi.org/10.1038/201068a0
   Web of Science ®Google Scholar
• Szafran, M.; Komasa, A.; Adamska, E. B. J. Mol. Struct. Theochem. 2007, 827, 101–107. https://doi.org/10.1016/j.molstruc.2006.05.012
   Web of Science ®Google Scholar
• Arivazhagan, M.; Meenakshi, R. Spectrochim. Acta A. 2011, 82, 316. https://doi.org/10.1016/j.saa.2011.07.055
   Web of Science ®Google Scholar
• Mulliken, R. S. J. Chem. Phys. 1955, 23, 1833–1840. https://doi.org/10.1063/1.1740588
   Web of Science ®Google Scholar
• Balachandran, V.; Santhi, G.; Karpagam, V.; Lakshmi, A. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2013, 110, 130–140. https://doi.org/10.1016/j.saa.2013.03.021
   Web of Science ®Google Scholar
• Demir, S.; Tinmaz, F.; Dege, N.; Ilhan, I. O. J. Mol. Struct. 2016, 1108, 637–648. https://doi.org/10.1016/j.molstruc.2015.12.057
   Web of Science ®Google Scholar
• Senge Bymathias, O.; Fazekas, M.; Notaras Eleni, G. A.; Blau Werner, J.; Zawadzka, M.; Locos Oliver, B.; Ni Mhuircheartaigh, E. M. Adv. Mater. 2007, 19, 2737–2774. https://doi.org/10.1002/adma.200601850
   Web of Science ®Google Scholar
• Dhanabal, T.; Amirthaganesan, G.; Dhandapani, M. Optik. 2014, 125, 4341–4346. https://doi.org/10.1016/j.ijleo.2014.03.027
   Web of Science ®Google Scholar
• Geskin, V. M.; Lambert, C.; Bredas, J. L. J. Am. Chem. Soc. 2003, 125, 15651–15658. https://doi.org/10.1021/ja035862p
   PubMed Web of Science ®Google Scholar
• Nakano, M.; Fujita, H.; Takahata, M.; Yamaguchi, K. J. Am. Chem. Soc. 2002, 124. https://doi.org/10.1021/ja0115969
   Web of Science ®Google Scholar
• Suresh, S.; Arivuoli, D. Rev. Adv. Mater. Sci. 2012, 30, 243–253.
   Web of Science ®Google Scholar
• Patel, K. D.; Patel, U. H. J. Mol. Struct. 2017, 1128, 127–134. https://doi.org/10.1016/j.molstruc.2016.08.046
   Web of Science ®Google Scholar
• Agilandeswari, R.; Aditya Prasad, A.; Sivaraman, S.; Kalainathan, S.; Meenakshisundaram, S. P. Mol. Cryst. Liq. Cryst. 2016, 625(1). https://doi.org/10.1080/15421406.2015.1069477
   Web of Science ®Google Scholar
• National Committee for Clinical Laboratory Standards. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that grow aerobically, approved standard, M7A5, 5th ed.; National Committee for Clinical Laboratory Standards: Wayne, PA, 2000.
   Google Scholar