Abstract

Two iron(III) tetraphenyl porphyrin catalytic units are connected by an azo-link to form the dimeric compound A. The compound A was then reacted with Pd 2+ to make a tetrameric iron(III) porphyrin complex B with all four iron(III) catalytic sites open to the substrates and reactants. Both the compounds were characterized spectroscopically and the results of homogeneous oxidation of some alkanes and alkenes with t-BuOOH in presence of catalytic quantities of A and B have indicated remarkable improvement in selectivity and efficiency of A over the monomeric catalyst and B over A.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call