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Solute–solvent interactions in solutions of 2-hydroxy-5-chloro-3-nitroacetophenone isonicotinoylhydrazone in N,N-dimethylformamide at 298–313 K according to ultrasonic and viscometric data

  • Chemical Thermodynamics and Thermochemistry
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Abstract

Density (ρ), speed of sound (u), and viscosity (η), measurements have been carried on 2-hydroxy- 5-chloro-3-nitroacetophenone isonicotinoylhydrazone (HCNAIH) in N,N-dimethylformamide at 298.15, 303.15, 308.15, and 313.15 K. Adiabatic compressibility (βs), intermolecular free length (L f), acoustic impedance (Z), internal pressure (P int), the apparent molar volume (V ф), limiting apparent molar volume (V ф 0), partial molar expansibility (ф 0E ), apparent molar adiabatic compressibility (K ф), limiting apparent molar adiabatic compressibility (K ф 0), viscosity B coefficients of Jones–Dole equation have been calculated. The activation free energy (Δμ 02 *) for viscous flow in solution have been calculated from B coefficient and partial molar volume data. The calculated parameters are used to interpret the solute–solvent interactions and structure forming/breaking ability of solute in DMF.

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References

  1. S. Rollas and S. G. Kucukguzel, Molecules 12, 1910 (2007).

    Article  CAS  Google Scholar 

  2. P. Vicini, M. Incerti, I. A. Doytchinova, P. La Colla, B. Busonera, and R. Loddo, Eur. J. Med. Chem. 41, 624 (2006).

    Article  CAS  Google Scholar 

  3. G. Tamasi, L. Chiasserini, L. Savini, A. Sega, and R. Cini, J. Inorg. Biochem. 99, 1347 (2005).

    Article  CAS  Google Scholar 

  4. S. S. Hussein, M. Mostafa, M. Safi, and A. Amin, Res. J. Chem. Sci. 3, 91 (2013).

    Google Scholar 

  5. P. V. Chalapathi, B. Prathima, S. Y. Rao, J. K. Reddy, G. N. Ramesh, V. D. Reddy, and V. A. Reddy, Res. J. Chem. Env. 15, 579 (2011).

    CAS  Google Scholar 

  6. A. Imramovsky, S. Polanc, J. Vinsova, M. Kocevar, J. Jampitek, Z. Reckova, and J. A. Kaustova, Bioorg. Med. Chem. 15, 2551 (2007).

    Article  CAS  Google Scholar 

  7. Y. Janin, Bioorg. Med. Chem. 15, 2479 (2007).

    Article  CAS  Google Scholar 

  8. C. ToitL, V. Pillay, and M. P. Danckwerts, Respi. Res. 7, 118 (2006).

    Article  Google Scholar 

  9. L. Savini, L. Chiasserini, V. Travagli, C. Pellerano, and E. Novellino, S. Consentino, and M. B. Pisano, Eur. J. Med. Chem. 39, 113 (2004).

    Article  CAS  Google Scholar 

  10. A. M. El-Hawash, W. A. Abdel, and M. A. El-Dewellawy, Archiv. Der. Pharm. 339, 14 (2006).

    Article  CAS  Google Scholar 

  11. M. T. Cocco, C. Congiu, V. Lilliu, and V. Onnis, Bioorg. Med. Chem. 14, 366 (2006).

    Article  CAS  Google Scholar 

  12. J. D. Pandye, A. Shukla, R. D. Rai, and K. Mishra, J. Chem. Eng. Data 34, 29 (1989).

    Article  Google Scholar 

  13. M. J. Iqbal and Q. M. Malik, J. Chem. Thermodyn. 37, 1347 (2005).

    Article  CAS  Google Scholar 

  14. P. Sharma, M. S. Chahan, S. Chauhan, and V. K. Syal, Ind. J. Pure Appl. Chem. 4, 839 (2008).

    Google Scholar 

  15. A. P. Mishra and S. K. Gautam, J. Ind. Chem. Soc. 79, 725 (2002).

    CAS  Google Scholar 

  16. A. Pal and S. Soni, J. Chem. Eng. Data 58, 18 (2013).

    Article  CAS  Google Scholar 

  17. C. Yang, H. Guanghu, H. Yifu, and M. Peisheng, J. Chem. Eng. Data. 53, 1639 (2008).

    Article  CAS  Google Scholar 

  18. P. S. Nikam and S. J. Kharat, J. Chem. Eng. Data. 50, 455 (2005).

    Article  CAS  Google Scholar 

  19. P. P. Venkatesu, M. Reddy, A. Kumar, and T. Hofman, J. Phys. Chem. 114, 6126 (2010).

    Article  Google Scholar 

  20. J. D. Pandey, N. Dubey, D. K. Dwivwdi, and R. Dey, Phys. Chem. Liq. 39, 781 (2001).

    Article  CAS  Google Scholar 

  21. A. Ali, A. K. Nain, and M. Kamil, Therm. Chim. Acta 274, 209 (1996).

    Article  CAS  Google Scholar 

  22. A. Pal, H. Kumar, R. Maan, and H. K. Sharma, Therm. Chim. Acta 590, 127 (2014).

    Article  CAS  Google Scholar 

  23. S. Nikam, A. B. Sawant, J. S. Aheer, and R. S. Khairnar, J. Ind. Chem. Soc. 77, 197 (2000).

    CAS  Google Scholar 

  24. H. D. Jenkins and B. Y. Marcus, Chem. Rev. 95, 2695 (1995).

    Article  CAS  Google Scholar 

  25. J. J. Wang, Z. N. Yan, H. C. Zhang, and J. S. Lu, Biophys. Chem. 86, 71 (2000).

    Article  CAS  Google Scholar 

  26. A. Pal and N. Chauhan, J. Mol. Liq. 149, 29 (2009).

    Article  CAS  Google Scholar 

  27. A. Ali, S. Hyder, S. Sabir, D. Chand, and A. K. Nain, J. Chem. Thermodyn. 38, 136 (2006).

    Article  CAS  Google Scholar 

  28. T. Srivastava, A. Pandey, R. Sethi, S. Haroon, J. D. Pandey, and K. Misra, Proc. Natl. Acad. Sci., Sec. A: Phys. Sci. 82, 179 (2012).

    Article  CAS  Google Scholar 

  29. Y. Zhang and Y. Batixie, J. Chem. Eng. Data. 52, 676 (2007).

    Article  CAS  Google Scholar 

  30. S. Bhanupriya, P. Ram, P. Rajwade, and R Pande, J. Chem. Eng. Data 53, 1458 (2008).

    Article  CAS  Google Scholar 

  31. D. Feakins, J. D. Freemantle, and K. G. Lawrence, J. Chem. Soc. Faraday Trans. 1, 70 (1974).

    Google Scholar 

  32. J. D. Pandey, A. K. Puri, A. Tewari, and A. K. Sharma, Proc. Ind. Acad. Sci. 111, 747 (1999).

    CAS  Google Scholar 

  33. T. Samanta and S. K. Saharay, J. Chem. Thermodyn. 42, 1131 (2010).

    Article  CAS  Google Scholar 

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Correspondence to A. S. Aswar.

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Dikkar, A.B., Pethe, G.B. & Aswar, A.S. Solute–solvent interactions in solutions of 2-hydroxy-5-chloro-3-nitroacetophenone isonicotinoylhydrazone in N,N-dimethylformamide at 298–313 K according to ultrasonic and viscometric data. Russ. J. Phys. Chem. 89, 2197–2203 (2015). https://doi.org/10.1134/S0036024415120109

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  • DOI: https://doi.org/10.1134/S0036024415120109

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