A Study of Kamlet–Taft β and π* Scales of Solvent Basicity and Polarity/Polarizability 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/s10953-020-00979-z.pdf
Reference17 articles.
1. 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)
2. Marenich, A.V., Jerome, S.V., Craner, C.J., Truhlar, D.G.: Charge Model 5: An extension of Hirshfeld population analysis for the accurate description of molecular interactions in gaseous and condensed phases. J. Chem. Theory Comput. 6, 527–541 (2012)
3. Kamlet, M.J., Taft, R.W.: The solvatochromic comparison method. I. The β-scale of solvent hydrogen-bond acceptor (HBA) basicities. J. Am. Chem. Soc. 98, 377–383 (1976)
4. Taft, R.W., Kamlet, M.J.: The solvatochromic comparison method. 2. The α-scale of solvent hydrogen-bond donor (HBD) acidities. J. Am. Chem. Soc. 98, 2886–2894 (1976)
5. Kamlet, M.J., Abboud, J.L., Taft, R.W.: The solvatochromic comparison method. 6. The π* scale of solvent polarities. J. Am. Chem. Soc. 99, 6027–6038 (1977)
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