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
chloroacetonitrileC2H2ClN0.000.341.01halo nitrile
N-methylacetamideC3H7NO0.470.801.01amide
nitrobenzeneC6H5NO20.000.301.01nitro aromatic
1-ethyl-3-methylimidazolium tetrafluoroborateC6H11BF4N20.700.261.03
thiolane-1-oxideC4H8OS0.000.811.06
1-ethyl-3-methyl-1H-imidazol-3-ium dicyanoazanideC8H11N50.530.351.08
1-ethyl-3-methylimidazolium acetateC8H14N2O20.400.951.09
waterH2O1.170.471.09
1-ethyl-3-methyl-1H-imidazol-3-ium perchlorateC6H11ClN2O40.560.411.11
1-ethyl-3-methylimidazolium nitrateC6H11N3O30.480.661.13
2-cyanopyridineC6H4N20.000.291.20nitrile heteroaromatic