posted on 2002-09-19, 00:00authored byMasako Abe, Youngjae You, Michael R. Detty
meso-Tetraphenyl-21-telluraporphyrins 3 and 4 act as catalysts for bromination reactions
with H2O2 and NaBr. Oxidation of telluraporphyrin 3 with excess H2O2 follows pseudo-first-order kinetics with a second-order rate constant of 0.85 ± 0.02 M-1 s-1 at 20.5 °C in 1:1
CH2Cl2/ethanol. Bromination of 4-pentenoic acid in two-phase mixtures of CH2Cl2 and pH 6
phosphate buffer with a stoichiometric amount of NaBr in the presence of a 50% excess of
H2O2 follows second-order kinetics as monitored by the loss of 4-pentenoic acid. Reactions
of 4-pentenoic acid and 1,3,5-trimethoxybenzene with excess H2O2 and excess NaBr follow
pseudo-first-order kinetics and are pseudo-first-order in bromide in two-phase mixtures.
Brominations of 4-pentenoic acid were conducted with initial concentrations of 0.2 M
4-pentenoic acid, 1.5 M H2O2, and 1.0 M in NaBr in a two-phase system of CH2Cl2 and pH
6 phosphate buffer. Brominations of 1,3,5-trimethoxybenzene were conducted with initial
concentrations of 0.2 M 1,3,5-trimethoxybenzene, 2.5 M H2O2, and 1.8 M in NaBr in a two-phase system of CH2Cl2 and pH 6 phosphate buffer. For both systems, telluraporphyrins 3
and 4 were added as catalysts at 0.2 mol % of substrate. Values of kcat for 3 were (4.0 ± 0.1)
× 10-2 M-2 s-1 for bromination of 4-pentenoic acid and (3.4 ± 0.2) × 10-2 M-2 s-1 for
bromination of 1,3,5-trimethoxybenzene. Turnover numbers for 3 were ≥2000 for bromination
of 4-pentenoic acid.