[1] F. Giannini, C. Devia, A. Rodr?guez, R. Enriz, F. Suvire, H. Baldoni, R. Furlan, S. Zacchino, The importance of keto-enol forms of arylpropanoids acting as antifungal compounds, Molecules 5 (2000) 580-582.[2] K. Iijima, A. Ohnogi, S. Shibata, The molecular structure of acetylacetone as studied by gas-phase electron diffraction, J. Mol. Struct. 156 (1987) 111-118.[3] R. Boese, M.Y. Antipin, D. Blaeser, K.A. Lyssenko, Molecular crystal structure of acetylacetone at 210 and 110 K: is the crystal disorder static or dynamic? J. Phys. Chem. B 102 (1998) 8654-8660.[4] V. Mohacek-Grosev, K. Furic, H. Lvankovic, Luminescence and Raman spectra of acetylacetone at low temperatures, J. Phys. Chem. A 111 (2007) 5820-5827.[5] J.L. Burdett, M.T. Rogers, Keto-enol tautomerism in β-dicarbonyls studied by nuclear magnetic resonance spectroscopy. I. Proton chemical shifts and equilibrium constants of pure compounds, J. Am. Chem. Soc. 11 (1964) 2105-2109.[6] M.T. Rogers, J.L. Burdett, Keto-enol tautomerism β-dicarbonyls studied by nuclear magnetic resonance spectroscopy. II. Solvent effects on proton chemical shifts and on equilibrium constants, Can. J. Chem. 43 (1965) 1516-1526.[7] J.N. Spencer, E.S. Holmboe, M.R. Kirshenbaum, D.W. Firth, P.B. Pinto, Solvent effects on the tautomeric equilibrium of 2,4-pentanedione, Can. J. Chem. 60 (1982) 1178-1182.[8] J.J. Dannenberg, R. Rios, Theoretical study of the enolic forms of acetylacetone. How strong is the hydrogen bond? J. Phys. Chem. 98 (1994) 6714-6715.[9] S. Schlund, E.M. Basilio Janke, K.Weisz, B. Engels, Predicting the tautomeric equilibrium of acetylacetone in solution. I. The right answer for the wrong reason? J. Comput. Chem. 31 (2000) 665-670.[10] T. Ishida, F. Hirata, S. Kato, Thermodynamic analysis of the solvent effect on tautomerization of acetylacetone: an ab initio approach, J. Chem. Phys. 110 (1999) 3938-3945.[11] Z. Rappoport (Ed.), The Chemistry of Enols, John Wiley & Sons, New York, 1990.[12] B.K. Rout, N.C. Mishra, V. Chakravortty, Viscosity and density of binary liquid mixtures of tri-n-butyl phosphate + benzene, +carbon tetrachloride, +isobutyl methyl ketone and + acetylacetone at 25, 30, 35, 40 and 45 ℃, Indian J. Chem. Technol. 1 (1994) 347-350.[13] R. Riggio, H.E. Martinez, N.Z. De Salas, Excess properties for acetylacetone + pentanols systems at 298.15 K, Can. J. Chem. 70 (1992) 2859-2863.[14] D.V.S. Jain, S.B. Saini, V. Chaudhry, Excess volumes of mixing for binary mixtures of acetylacetone, anisole, acrylonitrile and tetrahydrofuran with tetrachloroethylene and of tetrahydrofuran with carbon tetrachloride, Indian J. Chem. Sect A 18 (1979) 198-200.[15] M.M. Naoum, M.G. Botros, Excessmolar volumes and excess molecular polarizations of acetylacetone in nonpolar solvents, cyclohexane, carbon tetrachloride, benzene and dioxane, Indian J. Chem. Sect A 25 (1986) 1084-1088.[16] D.V.S. Jain, R.K. Wadi, S.B. Saini, J. Singh, Excess volume of mixing for binary mixtures of pyridine, acrylonitrile, anisole and acetylacetone with carbon tetrachloride, Indian J. Chem. Sect A 16 (1978) 561-563.[17] M. Kato, N. Suzuki, Excess volumes of binary mixtures containing acetylacetone, J. Chem. Thermodyn. 10 (1978) 435-440.[18] B.K. Rout, V. Chakravortty, Molecular interaction study on binary mixtures of acetylacetone fromthe excess properties of ultrasonic velocity, viscosity and density at various temperatures, Indian J. Chem. Sect A 33 (1994) 303-307.[19] L.P. Chen, H.-D. Lüdemann, Influence of conformational equilibria upon the selfdiffusion of the conformers in neat liquids, Z. Naturforsch. 55 (2000) 605-608.[20] X.J. Chen, R.Q. Hu, H.J. Feng, L.P. Chen, H.D. Lüdemann, Intradiffusion, density, and viscosity studies in binary liquid systems of acetylacetone + alkanols at 303.15 K, J. Chem. Eng. Data 57 (2012) 2401-2408.[21] K.F. Morris, C.S. Johnson Jr., Diffusion-ordered two-dimensional nuclear magnetic resonance spectroscopy, J. Am. Chem. Soc. 114 (1992) 3139-3141.[22] E.O. Stejskal, J.E. Tanner, Spin diffusion measurements: spin echoes in the presence of a time-dependent field gradient, J. Chem. Phys. 42 (1965) 288-292.[23] M.D. Pelta, G.A. Morris, M.J. Stchedroff, S.J. Hammond, A one-shot sequence for high-resolution diffusion-ordered spectroscopy, Magn. Reson. Chem. 40 (2002) S147-S152.[24] P.S. Nikam, B.S. Jagdale, A.B. Sawant, M. Hasan, Densities and viscosities for binary mixtures of benzonitrile with methanol, ethanol, propan-1-ol, butan-1-ol, pentan-1-ol, and 2-methylpropan-2-ol at (303.15, 308.15, and 313.15) K, J. Chem. Eng. Data 45 (2000) 214-218.[25] J.G. Baragi, M.I. Aralaguppi, T.M. Aminabhavi, M.Y. Kariduraganavar, A.S. Kittur, Density, viscosity, refractive index, and speed of sound for binary mixtures of anisole with 2-chloroethanol, 1,4-dioxane, tetrachloroethylene, tetrachloroethane, DMF, DMSO, and diethyl oxalate at (298.15, 303.15, and 308.15) K, J. Chem. Eng. Data 50 (2005) 910-916.[26] C. Yang, Y. Sun, Y. He, P.Ma, Volumetric properties and viscosities of binarymixtures of N,N'-dimethylformamide with methanol and ethanol in the temperature range (293.15 to 333.15) K, J. Chem. Eng. Data 53 (2008) 293-297.[27] A.Marchetti, C. Preti, M. Tagliazucchi, L. Tassi, G. Tosi, The N, N-dimethylformamide/ ethane-1,2-diol solvent system. Density, viscosity, and excess molar volume at various temperatures, J. Chem. Eng. Data 36 (1991) 360-365.[28] N.G. Tsierkezos, A.E. Kelarakis, M.M. Palaiologou, Densities, viscosities, refractive indices, and surface tensions of dimethyl sulfoxide + butyl acetate mixtures at (293.15, 303.15, and 313.15) K, J. Chem. Eng. Data 45 (2000) 395-398.[29] M.I. Aralaguppi, C.V. Jadar, T.M. Aminabhavi, Density, refractive index, viscosity, and speed of sound in binary mixtures of cyclohexanone with benzene, methylbenzene, 1,4-dimethylbenzene, 1,3,5-trimethylbenzene, and methoxybenzene in the temperature interval (298.15 to 308.15) K, J. Chem. Eng. Data 44 (1999) 446-450.[30] H.J.V. Tyrrell, K.R. Harris, Diffusion in Liquids. In a Theoretical and Experimental Study, Butterworths, London, 1984.[31] J. Gao, J.J. Pavelites, D. Habibollazadeh, Simulation of liquid amides using a polarizable intermolecular potential function, J. Phys. Chem. 100 (7) (1996) 2689-2697.[32] W.L. Jorgensen, C.J. Swenson, Optimized intermolecular potential functions for amides and peptides. Structure and properties of liquid amides, J. Am. Chem. Soc. 107 (1985) 569-578.[33] A. Laaksonen, P. Stilbs, P.E.Wasylishen, Molecular motion and salvation of benzene in water, carbon tetrachloride, carbon disulfide and benzene: a combined molecular dynamics simulation and nuclear magnetic resonance study, J. Chem. Phys. 108 (2) (1998) 455-468.[34] P. Backx, S. Goldman, H2O/D2O solubility isotope effects. An estimate of the extent of nonclassical rotational behavior of water, when dissolved in benzene or carbon tetrachloride, J. Phys. Chem. 85 (1981) 2975-2979.[35] O. Redlich, A. Kister, Thermodynamics of nonelectrolytic solutions. Algebraic representation of thermodynamic properties and the classification of solutions, J. Ind. Eng. Chem. 40 (1948) 345-348.[36] A. Estrada-Baltazar, M.G. Bravo-Sanchez, G.A. Iglesias-Silva, J.F.J. Alvarado, E.O. Castrejon-Gonzalez, M. Ramos-Estrada, Densities and viscosities of binary mixtures of n-decane+ 1-pentanol,+1-hexanol,+1-heptanol at temperatures from 293.15 to 363.15 K and atmospheric pressure, Chin. J. Chem. Eng. 23 (3) (2015) 559-571.[37] A.J. Treszczanowicz, O. Kiyohara, G.C. Benson, Excessmolar volumes for n-alkanes binary mixtures of decan-1-ol + n-pentane, +n-hexane, +n-octane, +n-decane, and + n-hexadecane, J. Chem. Thermodyn. 13 (1981) 253-260.[38] S.J. Tangeda, S. Nallani, Density and viscosity of binary liquid systems of N-methylacetamide with aromatic ketones at T = 308.15 K, J. Chem. Thermodyn. 38 (2005) 272-277.[39] R.P. Rastogi, J. Nath, J. Misra, Thermodynamics of weak interactions in liquid mixtures. II. Mixtures of carbon tetrachloride, benzene, o-xylene, and m-xylene, J. Phys. Chem. 71 (1967) 1277-1286. |