J. Blixt et C. Detellier, KINETICS AND MECHANISM OF THE SODIUM-CATION COMPLEXATION BY -TERT-BUTYL-25,26,27,28-TETRAMETHOXY-CALIX[4]ARENE IN SOLUTION, Journal of the American Chemical Society, 117(33), 1995, pp. 8536-8540
The kinetics and the mechanism of complexation of the sodium cation by
the title compound (1) were studied in a 1:1 (v/v) mixture of chlorof
orm and acetonitrile using Na-23 and 2D-EXSY H-1 NMR. The results show
the formation of a 1:1 complex where the calixarene is fixed in the c
one conformation, (Na,c)(+), with an equilibrium constant of formation
of (9.3 +/- 0.7) x 10(2) at 320 K with Delta H = -22 +/- 2 kJ mol(-1)
and Delta S = -7 +/- 5 J mol(-1) K-1. The exchange of the sodium cati
on between the solvated and the complexed sites follows a dissociation
/recombination mechanism, with a dissociation rate constant of 37.3 +/
- 0.4 s(-1) at 300 K. The kinetic parameters for the dissociation are
Delta H double dagger = 47 +/- 2 kJ mol(-1) and Delta S double dagger
= -61 +/- 6 J mol(-1) K-1. Calixarene 1 shows an intermediate behavior
between crown ethers and cryptands for the complexation processes of
the sodium cation in solution, dissociating with rates in the typical
orders of magnitude found for crown ethers, but with rates of formatio
n in the range of those typically found for cryptands.