Synthesis, crystal structure, spectral and thermal properties of 4-dimethylaminopyridinium salicylate monohydrate
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Abstract
4-dimethylaminopyridinium salicylate monohydrate (DMAPSA) was synthesized and its crystal structure was determined using single crystal X-ray diffraction analysis. From the crystal structure analysis it can be inferred that the crystal belongs to monoclinic system with space group of P21/n. Investigation has been carried out to assign the vibrational frequencies of the grown crystals by FTIR spectral studies. 1H and 13C FT–NMR has been recorded to elucidate the molecular structure. The molecular mass of DMAPSA has been measured using mass spectroscopic analysis. The thermal stability and thermal decomposition of DMAPSA have been investigated by means of thermogravimetric analysis and differential thermal analysis. The melting point of crystal was observed as 172 °C by melting point apparatus. Fluorescence spectra were taken for the excitation wavelength of 240 nm.
Keywords
Salicylic Acid Salicylate Differential Thermal Analysis Curve Grown Crystal Thermo GravimetricNotes
Acknowledgements
The authors are thankful to Dr. S. Moorthibabu, Crystal Growth Centre, Anna University for providing fluorescence studies and SAIF, IITM, Chennai for recording NMR spectrum, Mass spectrum and Single crystal data collection.
References
- 1.P.N. Prasad, D.J. Williams, Introduction to Nonlinear Optical Effects in Organic Molecules and Polymers (Wiley, New York, 1991) Google Scholar
- 2.D.S. Chemla, J. Zyss, Nonlinear Optical Properties of Organic Molecules and Crystals, vols. 1 and 2 (Academic Press, Orlando, 1987) Google Scholar
- 3.D.F. Eaton, Science 253, 281 (1991) ADSCrossRefGoogle Scholar
- 4.J.L. Moigne, L. Oswald, F. Kajzar, A. Thierry, Nonlinear Opt. 9, 187 (1995) Google Scholar
- 5.F. Brooks, Nucl. Instrum. Methods 162, 477 (1979) ADSCrossRefGoogle Scholar
- 6.Yu.A. Kaschuck, B. Esposito, L.A. Trykov, V.P. Semenov, Nucl. Instrum. Methods A 476, 511 (2002) ADSCrossRefGoogle Scholar
- 7.Y. Kachuk, B. Esposito, Nucl. Instrum. Methods A 551, 420 (2005) ADSCrossRefGoogle Scholar
- 8.S.P. Goswami, K. Ghosh, Tetrahedron Lett. 38, 4503 (1997) CrossRefGoogle Scholar
- 9.S.P. Goswami, A.K. Mahapatra, G.D. Nigam, K. Chinnakali, H.K. Fun, Acta Crystallogr. Sect. C 54, 1301 (1998) CrossRefGoogle Scholar
- 10.J.M. Lehn, Angew. Chem., Int. Ed. Engl. 29, 1304 (1990) CrossRefGoogle Scholar
- 11.M.J. Mladar, T.D. Vikic, Acta Pharm. 54, 177 (2004) Google Scholar
- 12.A.K. Sheinkman, S.I. Suminov, A.N. Kost, Russ. Chem. Rev. 42, 1409 (1973) CrossRefGoogle Scholar
- 13.B.B. Koleva, T. Kolev, R. Seidel, M. Spiteller, W.S. Sheldrick, Spectrochim. Acta, Part A, Mol. Biomol. Spectrosc. 71, 695 (2008) ADSCrossRefGoogle Scholar
- 14.Bruker-Nonius AXS, APEX2 and SAINT (Bruker-Nonius AXS, Madison, 2004) Google Scholar
- 15.G.M. Sheldrick, Acta Crystallogr. A 64, 112 (2008) ADSCrossRefGoogle Scholar
- 16.M. Hemamalini, H.K. Fun, Acta Crystallogr. E 66, o1418 (2010) CrossRefGoogle Scholar
- 17.H.K. Fun, C.S. Yeap, M.S. Siddegowda, H.S. Yathirajan, B. Narayana, Acta Crystallogr. E 67, o1584 (2011) CrossRefGoogle Scholar
- 18.H.H. Willard, L.L. Merritt Jr., J.A. Dean, F.A. Settle Jr., Instrumental Methods of Analysis, 6th edn. (Wadsworth, Belmont, 1986), p. 609 Google Scholar
- 19.D.T. McQuade, J. Kim, T.M. Swager, J. Am. Chem. Soc. 122, 5886 (2000) Google Scholar
- 20.H.G. Brittain, AAPS PharmSciTech 6, E448 (2005) CrossRefGoogle Scholar