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- Title
Basicity Limits of Neutral Organic Superbases.
- Authors
Leito, Ivo; Koppel, Ivar; Koppel, Ilmar A.; Tshepelevitsh, Sofja; Saame, Jaan; Kaupmees, Karl
- Abstract
The potential limits of superbasicity achievable with different families of neutral bases by expanding the molecular framework are explored using DFT computations. A number of different core structures of non-ionic organosuperbases are considered (such as phosphazenes, guanidinophosphazenes, guanidino phosphorus ylides). A simple model for describing the dependence of basicity on the extent of the molecular framework is proposed, validated, and used for quantitatively predicting the ultimate basicities of different compound families and the rates of substituent effect saturation. Some of the considered bases (guanidino phosphorus carbenes) are expected to reach gas-phase basicity around 370 kcal mol−1, thus being the most basic neutral bases ever reported. Also, the classical substituted alkylphosphazenes were predicted to reach p Ka values of around 50 in acetonitrile, which is significantly higher than previously expected.
- Subjects
SUPERBASES (Chemistry); BASICITY; DENSITY functional theory; CARBENES; PHOSPHAZENES
- Publication
Angewandte Chemie International Edition, 2015, Vol 54, Issue 32, p9262
- ISSN
1433-7851
- Publication type
Article
- DOI
10.1002/anie.201503345