Structural effects on the melting points of substituted alkanes, both branched and unbranched, ranging in length from 1 to 19 carbon atoms, were successfully correlated with a variant of the intermolecular force equation which included a variable capable of accounting for the packing energy contribution of the alkyl group. The final data set had 366 data points. The regression equation obtained accounted for 91·85% of the variance of the data with a standard error of 17·9 K. Twenty-nine data points could not be included in the correlation; nine of these are carboxamides. The contributions of the polar variables are slightly larger than those of the nonpolar variables while the contribution of structural variation in the substituent is greater than that in the alkyl group. It will be necessary to determine appropriate values of the packing parameter if compounds with chains longer than 20 carbon atoms are to be included in the model.
[1]
J. F. Liebman,et al.
ESTIMATING ENTROPIES AND ENTHALPIES OF FUSION OF ORGANIC COMPOUNDS
,
1991
.
[2]
M. Charton.
The quantitative description of small molecule binding to abiotic polymers
,
1988
.
[3]
S. Yalkowsky,et al.
Estimation of melting point of flexible molecules: Aliphatic hydrocarbons
,
1988
.
[4]
M. Charton.
Bulk and Steric Parameters in Binding and Reactivity of Bioactive Compounds
,
1984
.
[5]
M. Charton,et al.
The structural dependence of amino acid hydrophobicity parameters.
,
1982,
Journal of theoretical biology.
[6]
John Aurie Dean,et al.
Handbook of Organic Chemistry
,
1987
.