36611-02-6Relevant academic research and scientific papers
KINETICS OF THE REACTION OF THE 2,4,6-TRI-TERT-BUTYLPHENOXYL RADICAL WITH AROMATIC AMINES UNDER QUASIEQUILIBRIUM CONDITIONS, AND THE DISSOCIATION ENERGY OF THE N-H BOND IN AROMATIC AMINES
Varlamov, V. T.,Denisov, E. T.
, p. 657 - 662 (2007/10/02)
We have studied the kinetics of the reaction of the 2,4,6-tri-tert butylphenoxyl radical with 11 aromatic amines under quasiequilibrium conditions.The equilibrium constant for each amine was determined from the kinetic results.These values, together with their temperature dependence, were used to calculate the dissociation energy of the N-H bond in the 11 aromatic amines.By using earlier results for the reaction of the aroxyl radical with cumyl hydroperoxide, catalyzed by aromatic amines, we have calculated the rate constants for the reaction of 10 aminyl radicals with cumyl hydroperoxide and of cumylperoxy radicals with 10 aromatic amines.
The influence of the polymer matrix on the reactions of the nitroxyl radical with aromatic amines
Griva, A. P.,Denisova, L. N.,Denisov, E. T.
, p. 1429 - 1432 (2007/10/02)
The kinetics of the reactions of 4-benzoyloxy-2,2,6,6-tetramethylpiperidin-1-yloxy radical () with six aromatic amines in benzene and polypropylene (PP) have been investigated.It has been established that the reactions proceed bimolecularly in the kinetic region.The rate constants and activation energies for the reactions, and the frequencies of the rotational and translational diffusion of the radical under the experimental conditions have been measured.It has been shown that, on passing from the solution to PP, the reaction rate constants diminish and the activation energies increase and that in PP the reactivities of the amines are levelled out.There is a correlation between the rate constants and the molecular mobilities in the PP - benzene system.The following rule has been established for the first time: the greater the volume of the reactant (the amine), the greater the difference between the rate constants and activation energies for the reaction in the liquid phase and in the polymer.These features of the reactions in the solid phase have been explained in terms of the concept of the "rigid cage".The energy barrier which must be overcome by the reactants in PP in order to assume orientations favourable for the reaction has been calculated from the experimental data ( Vor = 8.5 - 13.5 kJmol-1 ; 333 K ).It has been observed that Vor increases with increasing volume of the reactant.The Gibbs free energy necessary to rearrange the form of the PP cage when the reaction of the radical with an amine takes place in it has been determined ( 33 kJ mol-1).
