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Spectrophotometric and Spectroscopic studies of charge transfer complexes of Benzamide as an electron donor with Picric acid as an electron acceptor in different polar solvents


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1 Department of Chemistry, Faculty of Science, Aligarh Muslim University, Aligarh -202002, India
     

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The charge transfer complexes of the donor benzamide (BZ) with &#960;-acceptor picric acid (PA) have been studied spectrophotometrically in various solvents such as carbon tetra chloride, ethanol, and methanol at room temperature using absorption spectrophotometer. The results indicate that formation of CTC in less polar solvent is high. The stoichiometry of the CT complex was found to be 1:1. The physical parameters of CT complex were evaluated by the Benesi-Hildebrand equation. The data are discussed in terms of formation constant (KCT), molar extinction coefficient (&#948;CT), standard free energy (G o ), oscillator strength(ƒ), transition dipole moment (&#181;EN), resonance energy (RN) and ionization potential (ID). The results indicate that the formation constant (K<SUB>CT</SUB>) for the complex were shown to be dependent upon the nature of electron acceptor, donor and polarity of solvents which were used. The results show that a charge transfer molecular complex between picric acid and benzamide stabilized by hydrogen bonding. The formation of the complex has been confirmed by UV-visible, FT-IR, 1 H-NMR, TGA/DTA spectral data methods. On the basis of the studies, the structure of CT complex is [(BZ) + (PA) −] , and a general mechanism for its formation is proposed.

Keywords

Charge Transfer complex, Benzamide (BZ), Picric acid (PA), UV-visible, FT-IR, 1H–NMR, TGA/DTA
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  • D.K. Roy, A. Saha, A.K. Mukherjee, Spectrochim. Acta Part A 61, 2005, 2017.
  • D.J. Brown, S.F. Mason, the Pyrimidines, Interscience Publishers, John Wiley and Sons, New York, 1962.
  • S.M. Sondhi, M. Johar, S. Rajvanshi, S.G. Dastodar, R. Shukla, R. Raghubir, J.W. Lown, Aust. J. Chem. 54, 2001, 169.
  • M. Kidwai, S. Saxena, S. Rastogi, R. Venkataramaman, Curr. Med. Chem. Ant- Infective Agents 2, 2004,269.
  • J.W. Park, B.A. Lee, S.Y. Lee, J. Phys. Chem. B 102, 1998, 8209.
  • P. Singh, P. Kumar, A. Katyal, R. Kalra, S.K. Dass, S. Prakash, R. Chandra, Spectrochim. Acta Part A 75, 2010, 983.
  • S.M. Teleb, A.S. Gaballa, M.A.F. Elmosallamy, E.M. Nour, Spectrochim. Acta Part A 61, 2005, 2708.
  • Y. Imai, K. Kamon, T. Kinuta, T. Sato, N. Tajima, R. Kuroda, Y. Matsubara, Eur. J. Org. Chem. 2009, 2519.
  • Y. Imai, K. Kamon, S. Kido, T. Sato, N. Tajima, R. Kuroda, Y. Matsubara, Eur. J. Org. Chem. 2008, 4784.
  • H. Kusama, H. Sugihara, J. Photochem. Photobiol. A 181, 2006, 268.
  • F.L. Zhao, B.Z. Xu, Z.Q. Zhang, S.Y. Tong, J. Pharm. Biomed. Anal. 21, 1999, 355.
  • A.S. Amin, A.M. El-Beshbeshy, Microchim. Acta 137, 2001, 63.
  • S.M. Andrade, S.M.B. Costa, R. Pansu, J. Colloids Interface Sci. 226, 2000, 260.
  • A. Eychmuller, A.L. Rogach, Pure Appl. Chem. 72, 2000, 179.
  • M. Hayashi, T.S. Yang, J. Yu, A. Mebel, S.H. Lin, J. Phys. Chem. A 101, 1997, 4156.
  • A.L. Sobolewski, W. Domcke, Chem. Phys. Lett. 315, 1999, 293.
  • H. Chen, Y.B. Jiang, Chem. Phys. Lett. 325, 2000, 605.
  • A. Romani, F. Ortica, G. Favaro, J. Photochem. Photobiol. A 135, 2000, 127.
  • K. Yamashita, S. Imahashi, J. Photochem. Photobiol. A 135, 2000, 135.
  • X. Wang, D.H. Levy, M.B. Rubin, S. Speisser, J. Phys. Chem. A 104, 2000, 6558.
  • I.M. Khan, A. Ahmad, Spectrochim. Acta Part A 73, 2009, 966.
  • N. Singh, I.M. Khan, A. Ahmad, Spectrochim. Acta Part A 75, 2010, 1347.
  • I.M. Khan, A. Ahmad, Mol. Cryst. Liq. Cryst. 515, 2009, 154.
  • J.M.A. Thumwood, A.C. Legon, Chem. Phys. Lett. 310, 1999, 88.
  • W. Jarzeba, S. Murata, M. Tachiya, Chem. Phys. Lett. 301, 1999, 347.
  • S. Jayanty, T.P. Radhakrishnan, Chem. Mater 13 (6), 2001, 2072.
  • C.C. Carvolho, A.J. Camargo, M.V. Teijido, P.C. Isolani, G. Vicentini, J. Zukermanschpecter, Zeitscrift Fur Krist. 218 (8), 2003, 575.
  • S.M. Teleb, A.S. Gaballa, Spectrochim. Acta Part A 62, 2005, 140.
  • A.S. Gaballa, C. Wagner, S.M. Teleb, E. Nour, M.A.F. Elmosallamy, G.N. Kaluderovic, H. Schmidt, D. Steinborn, J. Mol. Struct. 876, 2008, 301.
  • A. Chandramohan, R. Bharathikannan, M.A. Kandhaswamy, J. Chandrasekaran, V. Kandavelu, Cryst. Res. Technol. 43 (1), 2008, 93.
  • R. Bharathikannan, A. Chandramohan, M.A. Kandhaswamy, J. Chandrasekaran, R. Renganathan, V. Kandavelu, Cryst. Res. Technol. 43 (6), 2008, 683.
  • S. Yamagughi, M. Goto, H. Takhyanagi, H. Ogura, Bull. Chem. Soc. Jpn. 61,1988, 1026.
  • M. Paliwal, M.L. Kalrab, S.C. Ameta, J. Indian Chem. Soc. 85, 2008, 1038.
  • K.K. Kalninsh, G.M. Makhov, Russian J. Appl. Chem. 82, 2009, 563.
  • A.S. Aljabar, E. Nour, Spectrochim. Acta Part A 70, 2008, 997. 36. L. Pauling, The Nature of the Chemical Bond, Comell University Press, Ithaca, New York, 1960.
  • D.A. Skoog, Principle of international Analysis, 3 rd ed. Sannder College Publishing New York, 1985 (Chapter7).
  • M. Hasani, R.Alireza, Spectrochim. Acta Part A 65,2006, 1093.
  • S. Bhattacharya, K. Gosh, S.C, Momas. B. Spectrochim. Acta Part A 65, 2006, 659.
  • R. K. Gupta, R.A. Sig, J. Apple, Sci. 5 (1),2005, 28.
  • G. Aloisi, S. Pignataro, J. Chem. Soc. Faraday Trans. 69,1972, 534.
  • G. Briegleb, J.Czekalla, Z. Physikchem. (Frankfurt) 24, 1960, 237.
  • A.N. Martin, J. Swarbrick, A. Cammarata, Physical Pharmacy, 3rd
  • Ed, Lee and Febiger, Philadelphia, PA, 1969, 344.
  • G. Briegleb, Z. Angew. Chem. 76, 1964, 326.
  • H.A. Benesi, J. H. Hildebrand, J. Am. Chem. Soc. 7, 1949, 2703.
  • P. Douglas, G. Waechter, A. Mills, Photochem. Photobiol. 52, 1990, 473.
  • M., E. El – Zaria, Spectrochim.Acta A 69, 2008, 216.
  • R. Foster, T. J. Thomson, Trans. Faraday Soc. 58, 1962, 860.
  • L.J. Bellamy, The Infrared Spectra of Complex Molecules, Chapman and Hall, London, 1975.
  • M. S. Sivaramkumar, R. Velmurugan, M. Sekar, Drug Invention Today, 4(5), 2012, 375.
  • N. Singh, A. Ahmad, J. Mol. Struct. 977, 2010, 197.
  • I.M. Khan A. Ahmad, M. Oves, Spectrochim. Acta Part A 77, 2010, 1059.
  • S.R. Chaudhari, N. Suryaprakash J. Mol. Struct. 1016, 2012, 163

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  • Spectrophotometric and Spectroscopic studies of charge transfer complexes of Benzamide as an electron donor with Picric acid as an electron acceptor in different polar solvents

Abstract Views: 316  |  PDF Views: 2

Authors

Neeti Singh
Department of Chemistry, Faculty of Science, Aligarh Muslim University, Aligarh -202002, India
Afaq Ahmad
Department of Chemistry, Faculty of Science, Aligarh Muslim University, Aligarh -202002, India

Abstract


The charge transfer complexes of the donor benzamide (BZ) with &#960;-acceptor picric acid (PA) have been studied spectrophotometrically in various solvents such as carbon tetra chloride, ethanol, and methanol at room temperature using absorption spectrophotometer. The results indicate that formation of CTC in less polar solvent is high. The stoichiometry of the CT complex was found to be 1:1. The physical parameters of CT complex were evaluated by the Benesi-Hildebrand equation. The data are discussed in terms of formation constant (KCT), molar extinction coefficient (&#948;CT), standard free energy (G o ), oscillator strength(ƒ), transition dipole moment (&#181;EN), resonance energy (RN) and ionization potential (ID). The results indicate that the formation constant (K<SUB>CT</SUB>) for the complex were shown to be dependent upon the nature of electron acceptor, donor and polarity of solvents which were used. The results show that a charge transfer molecular complex between picric acid and benzamide stabilized by hydrogen bonding. The formation of the complex has been confirmed by UV-visible, FT-IR, 1 H-NMR, TGA/DTA spectral data methods. On the basis of the studies, the structure of CT complex is [(BZ) + (PA) −] , and a general mechanism for its formation is proposed.

Keywords


Charge Transfer complex, Benzamide (BZ), Picric acid (PA), UV-visible, FT-IR, 1H–NMR, TGA/DTA

References