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Apparent molar heat capacities and volumes,van der Waals volumes and accessible surface areas of alkylated derivatives of cytosine and uracil in aqueous solutions at 25°C.
Authors:A. Zielenkiewicz  G. Roux-Desgranges  A. H. Roux  J. P. E. Grolier  K. L. Wierzchowski  W. Zielenkiewicz
Affiliation:(1) Institute of Physical Chemistry of the Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa, Poland;(2) Laboratoire de Thermodynamique et Cinétique Chimique, URA CNRS 434, Université Blaise Pascal, 63177 Aubière Cedex, France;(3) Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-532 Warszawa, Poland
Abstract:Densities and specific heat capacities of aqueous solutions: 1,3,5,6-tetramethyluracil, 1,6-dimethyl-3-ethyluracil, 1,6-dimethyl-3-propyluracil, 1,6-dimethyl-3-butyluracil, 1,N4-trimethylcytosine, 1,N4-dimethyl-5-ethylcytosine, 1,N4 dimethyl-5-propylcytosine, 1,N4-dimethyl-5-butylcytosine were determined using flow calorimetry and flow densimetry at 25°C. Apparent molar volumes and heat capacities, van der Waals volumes and accessible surface areas were determined. It was stated that for alkylcytosines and alkyluracils partial molar volumes and heat capacities correlate linearly with the number of substituted methylene groups-CH2-as well as with the van der Waals volumes and accessible surface areas of the compounds studied; for cyclooligouracils the cyclization effect was discussed.
Keywords:Nucleic acid bases  uracil  cytosine  apparent molar heat capacities  apparent molar volumes  van der Waals volumes  accessible surface areas
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