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Improved Yukawa–Tsuno equation and the substituent effect on pyridine basicity
Author(s) -
Reis João Carlos R.,
Segurado Manuel A. P.,
Gomes de Oliveira Jaime D.
Publication year - 1998
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/(sici)1099-1395(199807)11:7<495::aid-poc28>3.0.co;2-k
Subject(s) - chemistry , pyridinium , substituent , pyridine , hammett equation , yukawa potential , computational chemistry , medicinal chemistry , reactivity (psychology) , taft equation , reaction rate constant , quantum mechanics , physics , medicine , alternative medicine , pathology , kinetics
An improved Yukawa–Tsuno equation was obtained by inserting the resonance demand parameter r in the tetralinear extension of the Hammett equation constrained by a hyperbolic relation between meta and para substituent effects. The new equation with five adjustable parameters and other Yukawa–Tsuno models were applied to selected literature data for the ionization equilibria of 21 meta ‐ and 20 para ‐substituted pyridinium ions in water at 25 °C. The data are best described by the new equation using either the sigma‐benzoic acid scale with r = 1.35 ± 0.16 or a truncated sigma‐plus scale (in which sigma‐zero constants are assigned to 4‐alkyl substituents) with r = 0.29 ± 0.04. Standard errors were estimated by Monte Carlo simulation. The results for the pyridinium ion demonstrate that the hyperconjugative effect by alkyl groups is inoperative and that through‐resonance effects by electron‐donating substituents are considerably hindered. The origin of this hindrance is ascribed to the particularities of nitrogen orbitals in heteroaromatic compounds. It is concluded that the pyridine reactivity lies between those of benzoic acid and benzylic cation, being much closer to the former. © 1998 John Wiley & Sons, Ltd.