Conformational studies by dynamic nuclear magnetic resonance. Part 16. The mechanism of tautomerism in triazenes

Abstract
The kinetics of tautomerism of triazenes, R1NH–NNR2 R1NN–NHR2, have been determined by means of line-shape analysis of the 1H n.m.r. spectra at various temperatures. When R1= R2= Me the equilibrium reaction is second-order whereas when R1= Me, R2= Ph or when R1= R2=p-MeC6H4 the reaction follows a first-order course. Thermodynamic activation parameters have been determined for both situations for a variety of solvents. Theoretical INDO calculations helped in understanding the switch from a bimolecular to a unimolecular reaction pathway when aliphatic are replaced by aromatic substituents. The absence of solvent effects suggests a radical mechanism, in agreement with the conclusion of a theoretical charge population analysis.

This publication has 0 references indexed in Scilit: