A Study of the Abraham Effective Solute Hydrogen Bond Basicity Parameter Using Computationally Derived Molecular Properties
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Molecular Biology,Biochemistry,Biophysics
Link
https://link.springer.com/content/pdf/10.1007/s10953-022-01168-w.pdf
Reference24 articles.
1. Abraham, M.H.: Scales of solute hydrogen-bonding: their construction and application to physicochemical and biochemical processes. Chem. Soc. Rev. 22, 73–83 (1993)
2. Abraham, M.H., Grellier, P.L., Prior, D.V., Morris, J.J., Taylor, P.J.: Hydrogen bondint. Part 10. A scale of solute hydrogen-bond basicity using log K values for complexation in tetrachloromethane. J. Chem. Soc. Perkin Trans 2 (1990). https://doi.org/10.1039/p29900000521
3. Waghorne, W.E., O’Farrell, C.: Solvent basicity, a study of Kamlet-Taft β and Gutmann DN values using computationally derived molecular properties. J. Solution Chem. 47, 1609–1625 (2018)
4. Waghorne, W.E.: A study of Kamlet-Taft β and π* scales of solvent basicity and polarity/polarizability using computationally derived molecular properties. J. Solution Chem. 49, 466–485 (2020). https://doi.org/10.1007/s10953-020-00979-z
5. Waghorne, W.E.: A study of the Reichardt parameter using solvent molecular properties derived from computational chemistry and consideration of the Kamlet and Taft α scale of solvent solvent hydrogen bond acidities. J. Solution Chem. 49, 1360–1372 (2020). https://doi.org/10.1007/s10953-020-01002-1
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2. Solvent Acidity and Basicity Scales: Analysis of Catalan’s SB and SA Scales and Gutmann’s Acceptor Number and Comparison with Kamlet and Taft’s β and α Solvent Scales, Gutmann’s Donor Number and Abraham’s B and A Solute Scales;Journal of Solution Chemistry;2024-04-30
3. Solvent Polarity/Polarizability Parameters: A Study of Catalan’s SPPN, Using Computationally Derived Molecular Properties, and Comparison with π* and ET(30);Liquids;2024-02-08
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