Compilation and critical evaluation of structure-reactivity parameters and equations: Part 2. Extension of the Hammett σ scale through data for the ionization of substituted benzoic acids in aqueous solvents at 25 C (Technical Report)
- 1 January 1997
- journal article
- Published by Walter de Gruyter GmbH
- Vol. 69 (12) , 2497-2510
- https://doi.org/10.1351/pac199769122497
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Influence of Substituents on Phenols Extraction and DissociationSeparation Science and Technology, 2012
- Organotrifluoroborate Hydrolysis: Boronic Acid Release Mechanism and an Acid–Base Paradox in Cross-CouplingJournal of the American Chemical Society, 2012
- Oxidation of styrene and of some derivatives with H2O2 catalyzed by novel imidazolium-containing manganese porphyrins: A mechanistic and thermodynamic interpretationJournal of Molecular Catalysis A: Chemical, 2011
- Substituent effects on the aromaticity of carbocyclic five-membered ringsPhysical Chemistry Chemical Physics, 2009
- On the Reactivity of C(sp3)–H σ‐Bonds: Oxygenation with Methyl(trifluoromethyl)dioxiraneEuropean Journal of Organic Chemistry, 2008
- Range of validity of the Hammett equation: acidity of substituted ethynylbenzenesNew Journal of Chemistry, 2006
- Homolytic bond dissociation energies of 4-substituted bicyclo[2.2.2]octanyl compounds: inductive/field effects on the stabilities of organic radicalsJournal of Physical Organic Chemistry, 2004
- A history of the international group for correlation analysis in chemistryJournal of Physical Organic Chemistry, 2003
- Infrared intensities of benzene derivatives as a measure of the substituent resonance effectJournal of Physical Organic Chemistry, 2001
- The reactivity of initiator radicalsPolymer, 1999