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Chalcones: A Solubility study at different temperatures

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Some new chalcones are synthesized by the condensation of aryl ketones with aromatic aldehydes and solubility of these synthesized chalcones is determined in chloroform and dichloromethane at temperatures ranging between 293.15 K and 313.15 K by gravimetric method. The experimental data was correlated well with modified Apelblat equation. Further, from the experimental solubility data, some thermodynamic parameters such as dissolution enthalpy, Gibb’s energy and entropy etc. were evaluated using van’t Hoff equation. The positive Gibb’s energy and negative entropy suggests spontaneous dissolution and more ordered structure in solution.
Rocznik
Tom
Strony
7--19
Opis fizyczny
Bibliogr. 39 poz., rys., tab., wz.
Twórcy
autor
  • Physical Chemistry Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
  • Physical Chemistry Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
  • Physical Chemistry Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
autor
  • Physical Chemistry Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
Bibliografia
  • [1] T. S. Straub. Tetrahedron Lett. 36 (1995) 663.
  • [2] S. Sandler, W. Karo, In Organic Functional Group Preparations 3 (1972) 372.
  • [3] S. N. López, et al., Bioorg. Med. Chem. 9 (2001) 1999.
  • [4] B. Baviskar, S. Patel, B. Baviskar, S. S. Khadabadi, M. Shiradkar, Asian J. Res. Chem. 1 (2008) 67.
  • [5] P. M. Sivakumar, S. Ganesan, P. Veluchamy, M. Doble, Chem. Biol. Drug. Des. 76 (2010) 407.
  • [6] F. Herencia, M. L. Ferrandiz, A. Ubeda, J. N. Domínguez, J. E. Charris, G. M. Lobo, M. J. Alcaraz, Bioorg. Med. Chem. Lett. 8 (1998) 1169.
  • [7] R. Kachadourian, B. J. Day, S. Pugazhenti, C. C. Franklin, E. Bastide , G. Mahaffey, C. Gauthier, A. Di-Pietro, A. Boumendjel, J. Med. Chem. 55 (2012) 1382.
  • [8] P. M. Sivakumar, T. D. Muthu Kumar, M .Toble, Chem. Biol. Drug Des. 74 (2009) 68.
  • [9] R. M. Mishra, A. Wahab, Ind. J. Hetero. Chem. 13 (2003) 29.
  • [10] T. Narsinghani, M. C. Sharma, S. Bhargav, Med Chem Res 22 (2013) 4059.
  • [11] C. A. Calliste, J. C. Le Bail, P. Trouillas, C. Pouget, G. Habrioux, A. J. Chulia, J. L. Duroux, Anticancer Res. 21(6A) (2001) 3949.
  • [12] T. Narender, T. Khaliq, S. Nishi, N. Goyal, S. Gupta, Bioorg. Med. Chem. 13 (2005) 6543.
  • [13] X. Wu, P. Wilairat, M. Go, Bioorg. Med. Chem. Lett. 12 (2002) 2299.
  • [14] A. Agarwal, K. Srivastava, S. K. Puri, M. S. Chauhan, Bioorg. Med. Chem. 13 (2005) 6226.
  • [15] P. M. Sivakumar, G. Babu, S. K. Mukesh, Chem. Pharm. Bull. 55 (2007) 44.
  • [16] Y. M. Lin, Y. Zhou, M. T. Flavin, L. M. Zhou, W. Nie, F.C. Chen, Bioorg. Med. Chem. 10 (2002) 2795.
  • [17] G. S, Viana, M. A Bandeira, F. J. Mantos, Phytomedicine 10 (2003) 189.
  • [18] Z. Nowakowska, Eur. J. Med. Chem. 42 (2007) 125.
  • [19] J. H. Cheng, C. F Hung, S. C. Yang, J. P. Wang, S. J. Won, C. N. Lin, Bioorg. Med. Chem. 16 (2008) 7270.
  • [20] S. Ducki, R. Forrest, J. A. Hadfield, A. Kendall, N. J. Lawrence, A.T. Mc-Gown, D. Rennison, Bioorg. Med. Chem. 8 (1998) 1051.
  • [21] G. Valdameri, et al., J. Med. Chem. 55 (2012) 3193.
  • [22] J. C. Jang, S. Lee, Y. Min, D. Lim, E. Jung, H. Oh, M. Oh, S. Jung, J. Med. Chem. 56 (2013) 6136.
  • [23] J. Gao, Z. W. Wang, D. M. Xu, R. K. Zhang, J. Chem. Eng. Data 52 (2007) 189.
  • [24] V. D. Athawale, P. Mathur, Experimental of Physical Chemistry 2001.19
  • [25] D. M. Aragon, M. A. Ruidiaz, E. F. Vargas, C. Bregni, D. A. Chiappetta, A. Sosnik, F. Martinez, J. Chem. Eng. Data 53 (2008) 2576.
  • [26] R. R. Krug, W. G. Hunter, R. A. Grieger, J. Phys. Chem. 80 (1976) 2341.
  • [27] P. Bustamante, S. Romero, A. Pena, B. Escalera, A. Reillo, J. Pharma. Sci. 87 (1998) 1590.
  • [28] P. S. Kalsi, Organic reactions and their mechanisms, New age international (P) limited- New Delhi, 2nd edition, 2004, 119.
  • [29] A. A. El-Bindary, A. Z. El-Sonbati, E. H. El-Mosalamy, R. M. Ahmed, Chem. Pap. 57 (2003) 255.
  • [30] S. John Joseph, et al., International Letters of Chemistry, Physics and Astronomy 5 (2014) 99-123.
  • [31] Sekar K. G., Thirunarayanan G., International Letters of Chemistry, Physics and Astronomy 8(3) (2013) 249-258.
  • [32] Ranganathan K., et al., International Letters of Chemistry, Physics and Astronomy 4 (2012)66-75.
  • [33] Arulkumaran R., et al., International Letters of Chemistry, Physics and Astronomy 5 (2013) 21-38.
  • [34] Sakthinathan S. P., et al., International Letters of Chemistry, Physics and Astronomy 6 (2013) 77-90.
  • [35] Sekar K. G., Thirunarayanan G., International Letters of Chemistry, Physics and Astronomy 8(2) (2013) 160-174.
  • [36] S. Vijayakumar, International Letters of Chemistry, Physics and Astronomy 9(1) (2013) 68-86.
  • [37] Thirunarayanan G., Sekar K. G., International Letters of Chemistry, Physics and Astronomy 10 (2013) 18-34.
  • [38] R. Sundararajan, et al., International Letters of Chemistry, Physics and Astronomy 1 (2014) 67-73.
  • [39] John Joseph S., et al., International Letters of Chemistry, Physics and Astronomy 4 (2014) 48-65.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-45fcc014-fb3a-4ac1-b260-a8c552203d3e
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