id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
admet-35	Dove, Stefan	Multivariate analysis of hydrophobic descriptors	2014	15	.pdf	application/pdf	7819	315	54	Beginning with the work of Collander [9], the correlation of log P values from different solvent-water systems and the decomposition of log P into more fundamental molecular descriptors like solubility, surface fractions, polarizability and hydrogen-bond strengths have contributed to quantitative structure- property analysis (QSPR) of hydrophobic effects (for review, see [4, 10]). Whereas meta- para positional effects on X and X-differences of inert substituents were only marginal, X-values of hydrogen-bonding, electron-attracting or -releasing substituents depend significantly on the nature of the functional group Y. Thus, log P values of disubstituted benzenes XPhY are not simply the sum of log P (benzene), X and Y from the benzene system, but include interaction increments due to electronic effects.	cache/admet-35.pdf	txt/admet-35.txt