Peer-reviewedCC BYCatalysis Science & Technology
Insight into the chemoselective aromatic vs. side-chain hydroxylation of alkylaromatics with H 2 O 2 catalyzed by a non-heme imine-based iron complex
Abstract
Side-chain/ring oxygenated product ratio increases upon decreasing the benzylic bond dissociation energy in the oxidation of alkylaromatics with H 2 O 2 catalyzed by an imine-based iron complex.
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BibTeX
@article{ticconi2026insight,
title = {{Insight into the chemoselective aromatic vs. side-chain hydroxylation of alkylaromatics with H 2 O 2 catalyzed by a non-heme imine-based iron complex}},
author = {Barbara Ticconi and Giorgio Capocasa and Andrea Cerrato and Stefano Di Stefano and Andrea Lapi and Beatrice Marincioni and Giorgio Olivo and Osvaldo Lanzalunga},
journal = {Catalysis Science \& Technology},
year = {2026},
month = oct,
doi = {10.1039/d0cy01868f},
url = {https://hal.science/hal-05786824v1},
note = {CC BY},
}
RIS
TY - JOUR
TI - Insight into the chemoselective aromatic vs. side-chain hydroxylation of alkylaromatics with H 2 O 2 catalyzed by a non-heme imine-based iron complex
AU - Barbara Ticconi
AU - Giorgio Capocasa
AU - Andrea Cerrato
AU - Stefano Di Stefano
AU - Andrea Lapi
AU - Beatrice Marincioni
AU - Giorgio Olivo
AU - Osvaldo Lanzalunga
PY - 2026
DA - 2026/10/08
JO - Catalysis Science & Technology
DO - 10.1039/d0cy01868f
UR - https://hal.science/hal-05786824v1
AB - Side-chain/ring oxygenated product ratio increases upon decreasing the benzylic bond dissociation energy in the oxidation of alkylaromatics with H 2 O 2 catalyzed by an imine-based iron complex.
SN - 2044-4753
ER -