Solid state conformational preferences of a flexible molecular backbone derived from acetone: dependence on electron donating/withdrawing ability of substitutions

S Varughese, SM Draper

Index: Varughese, Sunil; Draper, Sylvia M. Crystal Growth and Design, 2010 , vol. 10, # 5 p. 2298 - 2305

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Citation Number: 10

Abstract

Conformational pliability in a series of bis (phenyl) acetones exhibits a linear correlation with the Hammett constants of the substituents. The nature and morphology of the organic nano- /microparticles shows a direct dependence on the hydrophobic/hydrophilic character of the functional groups.