Substituent effects in tautomerism. Part 11. para-Substitution in N-phenylamidines
Abstract
U.v. spectroscopy shows that the tautomeric equilibria in N-phenylacetamidine and its p-methoxy- and p-nitroderivatives favour the imino N-aryl tautomers. Basicity measurements indicate pKT 2.4 for N-phenylacetamidine. The basicities of N′-aryl-NN-dimethylacetamidines correlate with σ substituent constants with ρ–3.60.