Kinetics and Mechanism of the Pyridinolysis of Aryl Furan-2-carbodithioates in Acetonitrile

Abstract

Kinetic studies on the pyridinolysis of aryl furan-2-carbodithioates 1 are carried out at 60.0 degrees C in acetonitrile. The biphasic rate dependence on the pyridine basicity with a breakpoint at pK(a) degrees = 5.2 is interpreted to indicate a change of the rate-limiting step from breakdown (beta(X) = 0.7-0.8) to formation (beta(X) = 0.2) of the tetrahedral intermediate, T(+/-), at the breakpoint as the basicity of the pyridine nucleophile is increased. Observation of the breakpoint is possible with pyridines since the expulsion rate of the pyridine (k(-)(a)) from T(+/-) is sufficiently low, with the low k(-)(a)/k(b) ratio leading to a low breakpoint, pK(a) degrees. The clear-cut change in the cross-interaction constants, rho(XZ), from a positive (rho(XZ) = +0.86) to a small negative (rho(XZ) = -0.11) value at the breakpoint supports the mechanistic change proposed. The magnitudes of rho(Z) and activation parameters are also consistent with the proposed mechanism.