Eur. Phys. J. E 4, 281-291
Reacting polymers with highly correlated initial conditionsO.V. Bychuk1, 2, B. O'Shaughnessy1 and N.J. Turro2
1 Department of Chemical Engineering, Columbia University, New York, NY 10027, USA
2 Department of Chemistry, Columbia University, New York, NY 10027, USA
(Received 18 May 2000)
We propose and theoretically study an experiment designed to measure short-time polymer reaction kinetics in melts or dilute solutions. The photolysis of groups centrally located along chain backbones, one group per chain, creates pairs of spatially highly correlated macroradicals. We calculate time-dependent rate coefficients governing their first-order recombination kinetics, which are novel on account of the far-from-equilibrium initial conditions. In dilute solutions (good solvents) reaction kinetics are intrinsically weak, despite the highly reactive radical groups involved. This leads to a generalised mean-field kinetics in which the rate of radical density decay , where is the equilibrium return probability for 2 reactive groups, given initial contact. Here is the correlation hole exponent for self-avoiding chain ends. For times beyond the longest coil relaxation time , remains true, but center of gravity coil diffusion takes over with rms displacement of reactive groups and . At the shortest times ( s), recombination is inhibited due to spin selection rules and we find . In melts, kinetics are intrinsically diffusion-controlled, leading to entirely different rate laws. During the regime limited by spin selection rules, the density of radicals decays linearly, . At longer times the standard result (for randomly distributed ends) is replaced by for these correlated initial conditions. The long-time behavior, , has the same scaling form in time as for dilute solutions.
82.35.+t - Polymer reactions and polymerization.
82.40.-g - Chemical kinetics and reactions: Special regimes and techniques.
© EDP Sciences, Società Italiana di Fisica, Springer-Verlag 2001