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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S. Rollas and S. G. Kucukguzel, Molecules 12, 1910 (2007).
P. Vicini, M. Incerti, I. A. Doytchinova, P. La Colla, B. Busonera, and R. Loddo, Eur. J. Med. Chem. 41, 624 (2006).
G. Tamasi, L. Chiasserini, L. Savini, A. Sega, and R. Cini, J. Inorg. Biochem. 99, 1347 (2005).
S. S. Hussein, M. Mostafa, M. Safi, and A. Amin, Res. J. Chem. Sci. 3, 91 (2013).
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).
A. Imramovsky, S. Polanc, J. Vinsova, M. Kocevar, J. Jampitek, Z. Reckova, and J. A. Kaustova, Bioorg. Med. Chem. 15, 2551 (2007).
Y. Janin, Bioorg. Med. Chem. 15, 2479 (2007).
C. ToitL, V. Pillay, and M. P. Danckwerts, Respi. Res. 7, 118 (2006).
L. Savini, L. Chiasserini, V. Travagli, C. Pellerano, and E. Novellino, S. Consentino, and M. B. Pisano, Eur. J. Med. Chem. 39, 113 (2004).
A. M. El-Hawash, W. A. Abdel, and M. A. El-Dewellawy, Archiv. Der. Pharm. 339, 14 (2006).
M. T. Cocco, C. Congiu, V. Lilliu, and V. Onnis, Bioorg. Med. Chem. 14, 366 (2006).
J. D. Pandye, A. Shukla, R. D. Rai, and K. Mishra, J. Chem. Eng. Data 34, 29 (1989).
M. J. Iqbal and Q. M. Malik, J. Chem. Thermodyn. 37, 1347 (2005).
P. Sharma, M. S. Chahan, S. Chauhan, and V. K. Syal, Ind. J. Pure Appl. Chem. 4, 839 (2008).
A. P. Mishra and S. K. Gautam, J. Ind. Chem. Soc. 79, 725 (2002).
A. Pal and S. Soni, J. Chem. Eng. Data 58, 18 (2013).
C. Yang, H. Guanghu, H. Yifu, and M. Peisheng, J. Chem. Eng. Data. 53, 1639 (2008).
P. S. Nikam and S. J. Kharat, J. Chem. Eng. Data. 50, 455 (2005).
P. P. Venkatesu, M. Reddy, A. Kumar, and T. Hofman, J. Phys. Chem. 114, 6126 (2010).
J. D. Pandey, N. Dubey, D. K. Dwivwdi, and R. Dey, Phys. Chem. Liq. 39, 781 (2001).
A. Ali, A. K. Nain, and M. Kamil, Therm. Chim. Acta 274, 209 (1996).
A. Pal, H. Kumar, R. Maan, and H. K. Sharma, Therm. Chim. Acta 590, 127 (2014).
S. Nikam, A. B. Sawant, J. S. Aheer, and R. S. Khairnar, J. Ind. Chem. Soc. 77, 197 (2000).
H. D. Jenkins and B. Y. Marcus, Chem. Rev. 95, 2695 (1995).
J. J. Wang, Z. N. Yan, H. C. Zhang, and J. S. Lu, Biophys. Chem. 86, 71 (2000).
A. Pal and N. Chauhan, J. Mol. Liq. 149, 29 (2009).
A. Ali, S. Hyder, S. Sabir, D. Chand, and A. K. Nain, J. Chem. Thermodyn. 38, 136 (2006).
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).
Y. Zhang and Y. Batixie, J. Chem. Eng. Data. 52, 676 (2007).
S. Bhanupriya, P. Ram, P. Rajwade, and R Pande, J. Chem. Eng. Data 53, 1458 (2008).
D. Feakins, J. D. Freemantle, and K. G. Lawrence, J. Chem. Soc. Faraday Trans. 1, 70 (1974).
J. D. Pandey, A. K. Puri, A. Tewari, and A. K. Sharma, Proc. Ind. Acad. Sci. 111, 747 (1999).
T. Samanta and S. K. Saharay, J. Chem. Thermodyn. 42, 1131 (2010).
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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