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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  -