Physics and Materials Chemistry
ISSN (Print): 2372-7098 ISSN (Online): 2372-7101 Website: http://www.sciepub.com/journal/pmc Editor-in-chief: Apply for this position
Open Access
Journal Browser
Go
Physics and Materials Chemistry. 2013, 1(1), 1-4
DOI: 10.12691/pmc-1-1-1
Open AccessArticle

Acoustical Studies of Some Derivatives of Azomethines in Methanol and N, N-Dimethylformamide at 303.15 K

Kapil Bhesaniya and Shipra Baluja,

Pub. Date: March 15, 2013

Cite this paper:
Kapil Bhesaniya and Shipra Baluja. Acoustical Studies of Some Derivatives of Azomethines in Methanol and N, N-Dimethylformamide at 303.15 K. Physics and Materials Chemistry. 2013; 1(1):1-4. doi: 10.12691/pmc-1-1-1

Abstract

The acoustical parameters of some synthesized azomethines have been studied from ultrasonic velocity and density measurement at different concentration in methanol and dimethyl formamide at 303.15 K. The apparent adiabatic molar compressibilities and apparent molar volume were also evaluated. The results provide useful information about solute-solute and solute-solvent interactions and are of significant help in understanding the behavior of synthesized compounds in solutions.

Keywords:
azomethines ultrasonic velocities apparent adiabatic molar compressibility apparent molar volume methanol dimethyl- formamide

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Figures

Figure of 4

References:

[1]  J. Salimon, N. Salih, E. Yousif, A. Hameed, and H. Ibraheem. “Synthesis, Characterization and Biological Activity of Schiff Bases of 2, 5-Dimercapto-1, 3, 4-thiadiazole’’, Aus. J. Bas. Appl. Sci., 4(7) 2016-2021, 2010.
 
[2]  N. Sari, S. Arslan, E. Lododlu and Ý. Pakiyan. “Antibacterial Activities of Some New Amino Acid-Schiff Bases”, G. U. J. Sci., 16(2) 283-288, 2003.
 
[3]  R. M. Patil,”Synthetic, structural and biological properties of binuclear complexes with some Schiff bases”, Acta Pol. Pharma. Drug Res., 64(4), 345-353, 2007.
 
[4]  P. Przybylski, A. Huczynski, K. Pyta, B. Brzezinski and F. Bartl, “Biological Properties of Schiff Bases and Azo Derivatives of Phenols”, Curr. Org. Chem., 13(2), 124-148, 2009.
 
[5]  A. Malik, S. Sher Khan, R. Wajid, H. Zonera, R. Abdur and I. Muhammad “Cytotoxic, antibacterial activity and physico-chemical properties of some acid catalyzed Schiff bases’’ Afr. J. Bio. 10(2), 209-213, 2011.
 
[6]  A. Cinarli1, D. Gürbüz1, A. Tavman1 and A. Seher Birteksöz, “Synthesis, spectral characterizations and antimicrobial activity of some Schiff bases of 4-chloro-2-aminophenol’’, Bull. Chem. Soc. Ethiop. 25(3), 407-417, 2011.
 
[7]  M. Gnana Ruba Priya, P. Panneerselvam and M. Karikalan. “Synthesis, characterisation and antibacterial, antifungal activities of Schiff bases of 4-(2-aminophenyl) morpholines’’ Int. J. Pharma. Biosci. 2(1), 267-272, 2011.
 
[8]  M. T. Tarafder, A. Kasbollah, N. Saravanan, K. A. Crouse, A. M. Ali and O. K. Tin, “S-methyldithiocarbazate and its Schiff bases: evaluation of bondings and biological properties”. J. Biochem. Mol. Biol. Biophys., 6(2), 85-91, 2002.
 
[9]  R. V. Ghadage and P.J. Shirote “Synthesis and anticonvulsant activity of Schiff’s bases of 3-{[2-({(E)-[(substituted) phenyl] methylidene} amino) ethyl] amino} quinoxalin-2(1H)-one’’ Bangladesh J. Pharmacol, 6, 92-99, 2011.
 
[10]  S. Baluja and S. Oza, “Ultrasonic studies of some derivatives of 6-ethylbenzene-1, 3-diol in 1,4-dioxane,” Fluid Phase Equilib, 208, 83-89, 2003.
 
[11]  S. Baluja, “Acoustical studies of some Schiff bases in 1, 4-dioxane and dimethylformamide at 318.15 K,” Chin. J. Chem., 24(10), 1327-1331, 2006.
 
[12]  N. Godvani, J. Movalia, R. Gajera and S. Baluja, “Study of molecular interactions of Loperamide drug in different solvents at 308.15 K”, Res. J. Pharma. Bio. Chem. Sci., 1, 67-73, 2010.
 
[13]  S. Baluja and F. Karia, “Ultrasonic velocity studies of solutions of some organic compounds at 298.15 K”, J. Chem. Bio. Phys. Sci., 2, 101-107, 2012.
 
[14]  J. A. Riddick, W. B. Bunger and T. Sakano, Organic “Solvents-Physical Properties and methods of purification,” Fourth Edition., Techniques of Chemistry, II, A Wiley-Interscience Publication, John Wiley. 1989.
 
[15]  J. O. Hirschfelder, C. F. Curtis and R. B. Bird, “Molecular Theory of Gases and Liquids”, Wiley, New York, 1964, Chapters 5 and 11.
 
[16]  J. S. Rowlinson and F. L. Swinton, “Liquid and Liquid Mixtures”, Butterworths, London, 3rd. edn., 16-17, 1982.
 
[17]  H. Falkenhagen and C. Bachem, “Compressibility of electrolytic solutions”, Nature (London, United Kingdom), 135, 830, 1935.
 
[18]  F. T. Gucker, “The apparent molal heat capacity, volume and compressibility of electrolytes”, Chem. Rev., 13, 111-130 (1933).
 
[19]  D. O. Masson, “Solute molecular volumes in relation to solvation and ionization”, Philos. Mag., 8, 218-235, 1929.
 
[20]  P. S. Nikam and A. R. Hiray, “Temperature and concentration dependence of ultrasonic velocity and allied parameters of monochloroacetic acid in ethanol-nitrobenzene mixtures”, Ind. J. Pure Appl. Phys., 29, 601-605, 1991.
 
[21]  M. Roy, V. Dakua, B. Sinha, “Partial molar volumes, viscosity B-coefficients, and adiabatic compressibilities of sodium molybdate in aqueous 1, 3-dioxolane mixtures from 303.15 to 323.15 K”. Int. J. Thermophys., 28, 1275-1284, 2007.
 
[22]  S. K. Choudhari, N. Yadav and S. S. Yadava, Ultrasonic viscosities and adiabatic compressibilities for the binary mixtures of methoxy benzene and several chlorohydrocarbons”, J. Pure Appl. Ultrason., 33, 43-45, 2011.