Abstract
Despite significantly different molecular structures and redox potentials, the electronic properties of the oxoferryl cation radical of 1 (M FeIV O instead of M FeIIICl, obtained by oxidation of 1 with m‐chloroperoxyben
zoic acid), which shows saddle‐shaped distortions as a result of its
peripheral chloro substituents, are similar to those of the
corresponding cation radical of the unsubstituted “planar” porphyrin.
These results help in the understanding of the different chemoand
regioselectivities of halogenated and halogen‐free iron porphyries in
the catalytic hydroxylation of alkanes. R 2,4,6 Me3C6H2.
| Original language | English |
|---|---|
| Journal | Angewandte Chemie International Edition in English |
| Volume | 32 |
| Issue number | 10 |
| Pages (from-to) | 1437-1439 |
| Number of pages | 3 |
| ISSN | 0570-0833 |
| DOIs | |
| Publication status | Published - 01.01.1993 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 9 Industry, Innovation, and Infrastructure
Fingerprint
Dive into the research topics of 'Oxoferryl π‐Cation Radical of β‐Pyrrole Octachlorinated meso‐Tetramesitylporphyrin: Electronic and Structural Properties'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver