Theoretical Studies of Solvent Effect on the Basicity of Substituted Pyridines
- 1 August 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 103 (34) , 7302-7307
- https://doi.org/10.1021/jp991115w
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Cavity size in reaction field theoryThe Journal of Chemical Physics, 1998
- Solvent Effects on the Barrier to C−N Bond Rotation in N,N-Dimethylaminoacrylonitrile: Modeling by Reaction Field Theory and by Monte Carlo SimulationsJournal of the American Chemical Society, 1998
- Kinetics and Mechanism of the Pyridinolysis of Phenyl Chloroformates in AcetonitrileThe Journal of Organic Chemistry, 1998
- Aminolysis of sulfamate esters in non-aqueous solvents. Evidence consistent with a concerted E2-type mechanismJournal of the Chemical Society, Perkin Transactions 2, 1996
- Amides. 3. Experimental and Theoretical Studies of the Effect of the Medium on the Rotational Barriers for N,N-Dimethylformamide and N,N-DimethylacetamideJournal of the American Chemical Society, 1995
- A new mixing of Hartree–Fock and local density-functional theoriesThe Journal of Chemical Physics, 1993
- Basicity of substituted 2-pyridyl-1,1,3,3-tetramethylguanidines and aminopyridines in acetonitrile and water solventsCanadian Journal of Chemistry, 1992
- Protonic Acidities and Basicities in the Gas Phase and in Solution: Substituent and Solvent EffectsPublished by Wiley ,1983
- Analysis of the acidities of 3- and 4-substituted pyridinium and anilinium ionsThe Journal of Organic Chemistry, 1981
- Ionic Reactions in AcetonitrilePublished by Wiley ,1967