Ultrasonic behavior of various chalcones in some solvents at different temperatures
Comportamiento ultrasónico de varias chalconas en algunos disolventes a diferentes temperaturas
DOI:
https://doi.org/10.15446/rcciquifa.v45n3.62014Palabras clave:
Ultrasonic velocity, chalcones, acoustical parameters, DMF, choloroform (en)Velocidad ultrasónica, chalconas, parámetros acústicos, DMF, cloroformo (es)
Descargas
Ultrasonic velocity, density and viscosity of some synthesized chalcones were measured in N,N-dimethyl formamide and chloroform at different temperatures (298.15 to 318.15 K). From these experimental data, various acoustical parameters such as specific impedance (Z), adiabatic compressibility (κs), Rao’s molar sound function (Rm), intermolecular free path length (Lf), solvation number (Sn), internal pressure (π) have been calculated in order to understand the molecular interactions
in the studied solutions. The results are interpreted in terms of molecular interactions occurring in the solutions.
La velocidad ultrasónica, la densidad y la viscosidad de soluciones de algunas chalconas sintéticas se midieron en N, N-dimetilformamida y cloroformo a diferentes temperaturas (desde 298,15 hasta 318,15 K). A partir de estos datos experimentales, se calcularon diversos parámetros acústicos tales como la impedancia específica (Z), la compresibilidad adiabática (ks), la función de sonido molar de Rao (Rm), la longitud de trayecto libre intermolecular (Lf), el número de solvatación (Sn) y la presión interna (Π), para comprender las interacciones moleculares en las soluciones estudiadas. Los resultados se interpretan en términos de las posibles interacciones moleculares que ocurren en las soluciones.
Referencias
(1) T. Sumathi, U. Maheswari, Ultrasonic and theoretical studies of some ternary liquid mixtures at various temperatures, Ind. J. Pure Appl. Physics, 47, 782-786 (2009).
(2) J.M. Thijssen, The history of ultrasound techniques in ophthalmology, Ultrasound Med. Biol., 19, 599-618 (1993).
(3) C.L. De Korte, M. Nillesen, A. Saris, R. Lopata, J. Thijssen, L. Kapusta, New developments in paediatric cardiac functional ultrasound imaging, J. Med. Ultrasonics, 41, 279-290 (2014).
(4) B.J. Staples, B.L. Roeder, G.A. Husseini, O. Badamjav, G.B Schaalje, W.G. Pitt, Role of frequency and mechanical index in ultrasonic enhanced chemotherapy in rats, Cancer Chemother. Pharmacol., 64, 593-600 (2009).
(5) R. Paproski, A. Forbrich, M. Hitt, R. Zemp, RNA biomarker release with ultrasound and phase-change nanodroplets, Ultrasound Med. Biol., 40, 1847-1856 (2014).
(6) W.P. Mason, Sonics and ultrasonics: Early history and applications, IEEE Trans Son. Ultrasonic, 23, 224 (1976).
(7) G. Gooberman, “Ultrasonics-Theory and application”, The English University Press Ltd., London EC4, 1968.
(8) V. Kühnel, U. Kaatze, Uncommon ultrasonic absorption spectra of "tetra alkyl ammonium bromides” in aqueous solution, J. Phys. Chem., 100, 19747-19757 (1996).
(9) M.R. Doosti, R. Kargar, M.H. Sayadi, Water treatment using ultrasonic assistance: A review, Proc. Int. Acad. Ecology. Environ. Sci., 2, 96-110 (2012).
(10) H.S. Lillard, Decontamination of poultry skin by sonication, Food Tech., 48, 72-73 (1994).
(11) Z. Dolatowski, J. Stadnik, D. Stasiak, Applications of ultrasound in food technology, Acta Scientiarum Polonorum, Technologia Alimentaria, 6, 89-99 (2007).
(12) S. Songül, C. Ysal, Use of ultrasound in food preservation, Nat. Sci., 5, 5-13 (2013).
(13) R. Palani, A. Geetha, S. Saravanan, S. Tontapur, Physico-chemical behavior of binary liquid mixtures of some monohydroxy alcohols with DMSO as common solvent, Rasayan J. Chem., 1, 481-488 (2008).
(14) A. Nain, D. Chand, Volumetric, ultrasonic and viscometric behavior of glycine, DL-alanine and L-valine in aqueous 1,4-butanediol solutions at different temperatures, J. Chem. Thermodyn., 41, 243-249 (2009).
(15) M. Gowrisankar, P. Venkateswarlu, K. Sivakumar, S, Sivarambabu, Ultrasonic studies on molecular interactions in binary mixtures of N-methyl aniline with methyl isobutylketone + 3-pentanone, and + cycloalkanones at 303.15 K, J. Solution Chem., 42, 916-935 (2013).
(16) R. Palani, A. Geetha, Acoustical and excess thermodynamic studies of molecular interaction in aqueous mixed solvent systems at 303, 308 and 313 K, Phys. Chem. Liq., 47, 542-552 (2009).
(17) X. Wu, R.T. Edward, L. Kostetski, N. Kocherginsky, A.L.C. Tan, P. Wilairat, M.L. Go, Antiplasmodial activity of ferrocenyl chalcones: Investigations into the role offerrocene, Eur. J. Pharm. Sci., 27, 175-187 (2006).
(18) B. Das, G. Mariappan, S. Saha, D. Bhowmik, Chiranjib, Anthelmintic and antimicrobial activity of some novel chalcone derivatives, J. Chem. Pharm. Res., 2, 113-112 (2010).
(19) T. Suwa, K. Fukushima, K. Kyogoku, Effect of an anti-ulcer agent, 2’- carboxymethoxy- 4,4’-bis(3-methyl-2-butenyloxy) chalcone (SU-88), on the biosynthesis of gastric sulfated mucosubstances in restrained and water-immersed rats, Jap. J. Pharm., 34, 89-94 (1984).
(20) K. Mallikarjun, Antiviral activity of substituted chalcones and their respective Cu(ii), Ni(ii) and Zn(ii) complexes, J. Chem., 2, 58-61 (2005).
(21) J. Jeon, S. Kim, C. Kim, J. Kim, J. Jun, Synthesis of biologically active chalcones and their anti-inflammatory effects, Bull. Korean Chem. Soc., 33, 953-957 (2012).
(22) O. Muraoka, T. Sawada, E. Morimoto, G. Tanabe, Chalcones as synthetic intermediates. A facile route to (±)-magnosalicin, an antiallergyneolignan, Chem. Pharm. Bull., 41, 772-774 (1993).
(23) S. Gafner, J. Wolfender, S. Mavi, K. Hostettmann, Antifungal and antibacterial chalcones from Myricaserrata, Planta Medica, 62(1), 67-90 (1996).
(24) S. Syam, S. Abdelwahab, M. Al-Mamary, S. Mohan, Synthesis of chalcones with anticancer activities, Molecules, 17, 617961-617995 (2012).
(25) Y. Rajendra Prasad, A. Srinivasa-Rao, R. Rambabu, Synthesis of some 4’-amino chalcones and their antiinflammatory and antimicrobial activity, Asian J. Chem., 21, 907-914 (2009).
(26) V. Mudalir, V. Joshi, Synthesis and insecticidal activity of new substituted phenoxychalocones, Ind. J. Chem., 34B, 456-457 (1995).
(27) E. Oganesyan, A. Saraf, A. Simonyan, I. Shriyaev, Structure-activity relationship in flavonoids. Anti-allergic activity of chalcones, Pharm. Chem. J., 25, 526-530 (1991).
(28) J. Riddick, W. Bunger, T. Sakano, “Organic solvents-physical properties and methods of purification Techniques of Chemistry”, Wiley-Interscience Publication, John Wiley, New York, 1986.
(29) G. Sastry, V. Satry, B. Krishnamurty, Ultrasonic parameters in mixed salt solutions, Ind. J. Pure Appl. Physics, 6, 637-638 (1986).
(30) B. Jacobson, A. Anderson, J. Arnold, A Proton magnetic resonance study of the hydration of deoxyribonucleic acid, Nature (London), 173, 772-773 (1954).
(31) S. Bagchi, S.K. Nema, R.P. Sing, Ultrasonic and rheological investigations of solid propellant binders, Eur. Polym. J., 25, 441-444 (1989).
(32) C.V. Suryanarayana, J. Kuppuswamy, Role of internal pressure in the chemistry of electrolyte solutions, J. Acoust. Soc., 9, 4-8 (1981).
Dimensions
PlumX
Visitas a la página del resumen del artículo
Descargas
Cómo citar
Licencia
Derechos de autor 2016 Revista Colombiana de Ciencias Químico-Farmacéuticas

Esta obra está bajo una licencia internacional Creative Commons Atribución 4.0.
El Departamento de Farmacia de la Facultad de Ciencias de la Universidad Nacional de Colombia autoriza la fotocopia de artículos y textos para fines de uso académico o interno de las instituciones citando la fuente. Las ideas emitidas por los autores son responsabilidad expresa de estos y no de la revista.
Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons de Atribución 4.0 aprobada en Colombia. Consulte la normativa en: http://co.creativecommons.org/?page_id=13




