Gutmann acceptor and donor numbers

The Gutmann Acceptor- (AN) and Donor Number (DN) are measures of the strength of solvents as Lewis acids or bases.
The Acceptor Number is based on the 31P-NMR chemical shift of triethylphosphine oxide in the solvent.
The Donor Number is based on the heat of reaction between the compound dissolved in CH2ClCH2Cl and SbCl5, and is therefore a 'solute' rather than a 'solvent' scale. Because SbCl5 is decomposed by protic compounds, e.g. alcohols, the Donor Numbers for these have to be determined by indirect methods.

The Acceptor Number is a measure of hydrogen bond acidity and correlated with other hydrogen bond acidity scales such as → Dimroth-Reichardt ET (→ ET vs AN) and → Swain Acity (→ Acity vs AN). Correlation with → Kamlet-Taft α and → Catalán SA is weaker.
The Donor Number is correlated with → Kamlet-Taft β (→ β vs DN).

See → "The donor-acceptor approach to molecular interactions" by V. Gutmann, Plenum Press, New York and London (1978), and →Lewis donor strength for scales of Lewis bases.

Note: AN values in parenthesis are estimated from the corresponding Dimroth-Reichardt ET-values.

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NameFormulaAcceptor number
AN
Donor number
DN
🏷 Tag
ethyl acetateC4H8O29.317.1ester;
methyl propanoate     ⋮(9.5)11.0ester;
sulfolaneC4H8O2S19.214.8
morpholineC4H9NO17.5ether; amine;
N,N-dimethylacetamide     ⋮13.627.8amide;
trimethylureaC4H10N2O29.3
2-methyl-1-propanolC4H10O(29.5)37.0alcohol;
2-methyl-2-propanol     ⋮27.138.0alcohol;
butanol     ⋮36.819.5alcohol;
diethyl ether     ⋮3.919.2ether;
methyl propyl ether     ⋮18.1ether;
1,2-dimethoxyethaneC4H10O210.220.0ether;
diethyl sulfideC4H10S(5.2)41.0
2-methyl-2-propanamineC4H11N(6.7)57.0amine;
butylamine     ⋮(8.8)42.0amine;
diethylamine     ⋮9.450.0amine;
pyridineC5H5N14.233.1heteroaromatic;
pyridine N-oxideC5H5NO34.4heteroaromatic;
cyclopentanoneC5H8O(12.2)18.0ketone;
N-methylpyrrolidoneC5H9NO13.327.3amide;
1-methylpyrrolidin-2-thioneC5H9NS17.7
1,3-dimethyl-2-imidazolidinoneC5H10N2O(18.0)27.7amide;
2-methyltetrahydrofuranC5H10O(6.7)12.0ether;
2-pentanone     ⋮(15.4)17.5ketone;
3-methyl-2-butanone     ⋮(15.0)17.1ketone;