Endorsing Organic Porous Polymers in Regioselective and Unusual Oxidative C═C Bond Cleavage of Styrenes into Aldehydes and Anaerobic Benzyl Alcohol Oxidation via Hydride Elimination.

Abstract

Oxidative cleavage of styrene C═C double bond is accomplished by employing a nitrogen-rich triazine-based microporous organic polymer as an organocatalyst. We report this regioselective reaction as first of its kind with no metal add-ons to afford benzaldehydes up to 92% selectivity via an unusual Wacker-type C═C bond cleavage. Such a reaction pathway is generally observed in the presence of a metal catalyst. This polymer further shows high catalytic efficiency in an anaerobic oxidation reaction of benzyl alcohols into benzaldehydes. The reaction is mediated by a base via the in situ generation of hydride ions. This study is supported by experiments and computational analyses for a free-radical transformation reaction of oxidative C═C bond cleavage of styrenes and a hydride elimination mechanism for the anaerobic oxidation reaction. Essentially, the study unveils protruding applications of metal-free nitrogen-rich porous polymers in organic transformation reactions.