Source:http://linkedlifedata.com/resource/pubmed/id/17622172
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
|
pubmed:dateCreated |
2007-7-27
|
pubmed:abstractText |
Mechanistic studies of the aromatic hydroxylation by high-valent iron(IV)-oxo porphyrin pi-cation radicals revealed that the aromatic oxidation involves an initial electrophilic attack on the pi-system of the aromatic ring to produce a tetrahedral radical or cationic sigma-complex. The mechanism was proposed on the basis of experimental results such as a large negative Hammett rho value and an inverse kinetic isotope effect. By carrying out isotope labeling studies, the oxygen in oxygenated products was found to derive from the iron-oxo porphyrin intermediates.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0022-3263
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
3
|
pubmed:volume |
72
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
6301-4
|
pubmed:meshHeading |
pubmed-meshheading:17622172-Cations,
pubmed-meshheading:17622172-Chemistry, Organic,
pubmed-meshheading:17622172-Iron,
pubmed-meshheading:17622172-Kinetics,
pubmed-meshheading:17622172-Models, Chemical,
pubmed-meshheading:17622172-Molecular Conformation,
pubmed-meshheading:17622172-Porphyrins,
pubmed-meshheading:17622172-Spectrophotometry, Ultraviolet,
pubmed-meshheading:17622172-Time Factors
|
pubmed:year |
2007
|
pubmed:articleTitle |
Mechanistic insight into the aromatic hydroxylation by high-valent iron(IV)-oxo porphyrin pi-cation radical complexes.
|
pubmed:affiliation |
Department of Chemistry, Division of Nano Sciences, and Center for Biomimetic Systems, Ewha Womans University, Seoul 120-750, Korea.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|