Loading…
New mechanistic insight into intramolecular arene hydroxylation initiated by (μ-1,2-peroxo)diiron(iii) complexes with dinucleating ligandsElectronic supplementary information (ESI) available: Experimental details of synthesis and structural, spectroscopic, and kinetic data. CCDC 1430633 and 1430634. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5dt04088d
(μ-1,2-Peroxo)diiron( iii ) complexes ( 2 -R) with dinucleating ligands (R-L) generated from the reaction of bis(μ-hydroxo)diiron( ii ) complexes [Fe 2 (R-L)(OH) 2 ] 2+ ( 1 -R) with dioxygen in acetone at −20 °C provide a diiron-centred electrophilic oxidant, presumably diiron( iv )-oxo species, whi...
Saved in:
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | (μ-1,2-Peroxo)diiron(
iii
) complexes (
2
-R) with dinucleating ligands (R-L) generated from the reaction of bis(μ-hydroxo)diiron(
ii
) complexes [Fe
2
(R-L)(OH)
2
]
2+
(
1
-R) with dioxygen in acetone at −20 °C provide a diiron-centred electrophilic oxidant, presumably diiron(
iv
)-oxo species, which is involved in aromatic ligand hydroxylation.
Intramolecular arene hydroxylation initiated by (μ-1,2-peroxo)diiron(
iii
) complexes (
2
-R) with dinucleating ligands (R-L) involves a diiron(
iv
)-oxo species. |
---|---|
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c5dt04088d |