Abstract
The mechanism of carbon-carbon bond scission by 'iron sulfide' catalysts is explored through the use of substituted diphenylmethane model compounds. The reaction kinetics are shown to be first order in model compound with the methylene-arene carbon-carbon bond adjacent to the most substituted arene being selectively cleaved. These results are consistent with the catalyst acting as a hydrogen atom transfer agent.
| Original language | English |
|---|---|
| Pages (from-to) | 105-111 |
| Number of pages | 7 |
| Journal | Catalysis Today |
| Volume | 31 |
| Issue number | 1-2 |
| Publication status | Published - Sep 5 1996 |
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Keywords
- Catalysis: Hydrogen transfer; Iron; Model compounds
ASJC Scopus subject areas
- Catalysis
- Process Chemistry and Technology
Cite this
Mechanistic investigations of iron/sulfur-catalyzed bond scission in aromatic hydrocarbons. a catalytic hydrogen atom transfer step involving a late transition state. / Autrey, Tom; Linehan, John; Camaioni, Donald M.; Kaune, Lauren E.; Watrob, Heather M.; Franz, James A.
In: Catalysis Today, Vol. 31, No. 1-2, 05.09.1996, p. 105-111.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Mechanistic investigations of iron/sulfur-catalyzed bond scission in aromatic hydrocarbons. a catalytic hydrogen atom transfer step involving a late transition state
AU - Autrey, Tom
AU - Linehan, John
AU - Camaioni, Donald M.
AU - Kaune, Lauren E.
AU - Watrob, Heather M.
AU - Franz, James A.
PY - 1996/9/5
Y1 - 1996/9/5
N2 - The mechanism of carbon-carbon bond scission by 'iron sulfide' catalysts is explored through the use of substituted diphenylmethane model compounds. The reaction kinetics are shown to be first order in model compound with the methylene-arene carbon-carbon bond adjacent to the most substituted arene being selectively cleaved. These results are consistent with the catalyst acting as a hydrogen atom transfer agent.
AB - The mechanism of carbon-carbon bond scission by 'iron sulfide' catalysts is explored through the use of substituted diphenylmethane model compounds. The reaction kinetics are shown to be first order in model compound with the methylene-arene carbon-carbon bond adjacent to the most substituted arene being selectively cleaved. These results are consistent with the catalyst acting as a hydrogen atom transfer agent.
KW - Catalysis: Hydrogen transfer; Iron; Model compounds
UR - http://www.scopus.com/inward/record.url?scp=0041181429&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0041181429&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0041181429
VL - 31
SP - 105
EP - 111
JO - Catalysis Today
JF - Catalysis Today
SN - 0920-5861
IS - 1-2
ER -