Kamlet-Taft solvent parameters

There are three Kamlet-Taft solvent parameters: α (hydrogen bond donor), β (hydrogen bond acceptor), and π* (polarizability).
The values of α have been set to 0 for solvents that are assumed to be unable to donate hydrogen bonds. This truncation at 0 is the main reason it differs from other measures of hydrogen bond acidity such as ET and AN.

Occasionally a "polarity correction term" (fudge factor), δ, is seen in correlations. For aromatics δ=1.0, for polychlorinated compounds δ=0.5, and for all other solvents δ=0.0 . If possible this type of ad hoc parameters should be avoided and separate correlations used for different solvent classes.

α is correlated with →Dimroth-Reichardt ET (→ET vs α) and →Gutmann AN (→AN vs α).
β is correlated with →Gutmann DN (→DN vs β) except for amines and sulfides.
π* is correlated with →Catalán SPP (→SPP vs π*).

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NameFormulaαβπ*🏷 Tag
4-methylphenolC7H8O1.640.340.68
1,3-dioxolaneC3H6O20.000.450.69
ethoxybenzeneC8H10O0.000.300.69aromatic ether
ethyl chloroacetateC4H7ClO20.000.350.70halo ester
2-propanoneC3H6O0.080.430.71ketone
butanenitrileC4H7N0.000.400.71nitrile
chlorobenzeneC6H5Cl0.000.070.71aromatic halo
propanenitrileC3H5N0.000.390.71nitrile
3-pentanoneC5H10O0.000.450.72ketone
dimethylcyanamideC3H6N20.000.640.72
phenolC6H6O1.650.300.72
triethyl phosphateC6H15O4P0.000.770.72
trimethyl phosphateC3H9O4P0.000.770.72
2,2,2-trifluoroethanolC2H3F3O1.510.000.73halo alcohol
3,4-dimethylpyridineC7H9N0.000.780.73heteroaromatic
anilineC6H7N0.260.500.73aromatic amine
methoxybenzeneC7H8O0.000.320.73aromatic ether
N,N-dimethylanilineC8H11N0.000.430.73amine aromatic
ethyl benzoateC9H10O20.000.410.74aromatic ester
1,2-dibromoethaneC2H4Br20.000.000.75halo
1,3-dichlorobenzeneC6H4Cl20.000.030.75aromatic halo
acetonitrileC2H3N0.190.400.75nitrile
1,1,3,3-tetramethylguanidineC5H13N30.000.860.76
acetic anhydrideC4H6O30.000.290.76
cyclohexanoneC6H10O0.000.530.76ketone