Insight into the chemoselective aromatic vs. side-chain hydroxylation of alkylaromatics with H2O2 catalyzed by a non-heme imine-based iron complex. Issue 1 (17th November 2020)

• Record Type: Journal Article
• Authors: Ticconi, Barbara; Capocasa, Giorgio; Cerrato, Andrea; Di Stefano, Stefano; Lapi, Andrea; Marincioni, Beatrice; Olivo, Giorgio; Lanzalunga, Osvaldo
• Is Part Of: Catalysis science & technology. Volume 11:Issue 1(2021)
• Page Start: 171
• Page End: 178
• Publication Date: 2020-11-17
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/d0cy01868f
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Side-chain/ring oxygenated product ratio increases upon decreasing the benzylic bond dissociation energy in the oxidation of alkylaromatics with H2 O2 catalyzed by an imine-based iron complex. Abstract : The oxidation of a series of alkylaromatic compounds with H2 O2 catalyzed by an imine-based non-heme iron complex prepared in situ by reaction of 2-picolylaldehyde, 2-picolylamine, and Fe(OTf)2 in a 2 : 2 : 1 ratio leads to a marked chemoselectivity for aromatic ring hydroxylation over side-chain oxidation. This selectivity is herein investigated in detail. Side-chain/ring oxygenated product ratio was found to increase upon decreasing the bond dissociation energy (BDE) of the benzylic C–H bond in line with expectation. Evidence for competitive reactions leading either to aromatic hydroxylation via electrophilic aromatic substitution or side-chain oxidation via benzylic hydrogen atom abstraction, promoted by a metal-based oxidant, has been provided by kinetic isotope effect analysis.