Reaction of lithium metal with benzil in THF. A kinetic study
The kinetics of benzil reduction by lithium metal in THF were investigated under different reaction conditions. The main reaction products were phenylacetophenone and bibenzyl; 1,2-diphenylethanol and diphenylethene were minor products. The first radical anion intermediate formed by electron transfe...
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2003
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v16_n10_p669_Nudelman http://hdl.handle.net/20.500.12110/paper_08943230_v16_n10_p669_Nudelman |
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paper:paper_08943230_v16_n10_p669_Nudelman2023-06-08T15:47:42Z Reaction of lithium metal with benzil in THF. A kinetic study Benzil Heterogenous systems Induction period Lithium metal Organolithium Surface reactions Electron spin resonance spectroscopy Electrons Organic compounds Reaction kinetics Induction periods Lithium The kinetics of benzil reduction by lithium metal in THF were investigated under different reaction conditions. The main reaction products were phenylacetophenone and bibenzyl; 1,2-diphenylethanol and diphenylethene were minor products. The first radical anion intermediate formed by electron transfer upon chemisorption of the benzyl on the metal surface was fully characterized and quantitatively determined by ESR spectroscopy. The kinetics of the benzil decay and of the formation of the two main products were followed by GC and ESR. A unique feature of this reaction is the presence of a well-defined and reproducible induction period. A mechanism is proposed which accounts for the main experimental observations. Copyright © 2003 John Wiley & Sons, Ltd. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v16_n10_p669_Nudelman http://hdl.handle.net/20.500.12110/paper_08943230_v16_n10_p669_Nudelman |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Benzil Heterogenous systems Induction period Lithium metal Organolithium Surface reactions Electron spin resonance spectroscopy Electrons Organic compounds Reaction kinetics Induction periods Lithium |
spellingShingle |
Benzil Heterogenous systems Induction period Lithium metal Organolithium Surface reactions Electron spin resonance spectroscopy Electrons Organic compounds Reaction kinetics Induction periods Lithium Reaction of lithium metal with benzil in THF. A kinetic study |
topic_facet |
Benzil Heterogenous systems Induction period Lithium metal Organolithium Surface reactions Electron spin resonance spectroscopy Electrons Organic compounds Reaction kinetics Induction periods Lithium |
description |
The kinetics of benzil reduction by lithium metal in THF were investigated under different reaction conditions. The main reaction products were phenylacetophenone and bibenzyl; 1,2-diphenylethanol and diphenylethene were minor products. The first radical anion intermediate formed by electron transfer upon chemisorption of the benzyl on the metal surface was fully characterized and quantitatively determined by ESR spectroscopy. The kinetics of the benzil decay and of the formation of the two main products were followed by GC and ESR. A unique feature of this reaction is the presence of a well-defined and reproducible induction period. A mechanism is proposed which accounts for the main experimental observations. Copyright © 2003 John Wiley & Sons, Ltd. |
title |
Reaction of lithium metal with benzil in THF. A kinetic study |
title_short |
Reaction of lithium metal with benzil in THF. A kinetic study |
title_full |
Reaction of lithium metal with benzil in THF. A kinetic study |
title_fullStr |
Reaction of lithium metal with benzil in THF. A kinetic study |
title_full_unstemmed |
Reaction of lithium metal with benzil in THF. A kinetic study |
title_sort |
reaction of lithium metal with benzil in thf. a kinetic study |
publishDate |
2003 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v16_n10_p669_Nudelman http://hdl.handle.net/20.500.12110/paper_08943230_v16_n10_p669_Nudelman |
_version_ |
1768542698049896448 |