Preconversion catalytic deoxygenation of phenolic functional groups. Quarterly technical progress report, January 1, 1992--March 31, 1992
The deoxygenation of phenols is a conceptually simple, but unusually difficult chemical transformation to achieve. The phenolic C-O bond energy of 103 kcal/mol is as strong as a benzene C-H bond and over a 10 kcal/mol stronger than the C-O bonds of methanol and ethanol. The consequence of this is that the hydrogenation/deoxygenation methods in current use require severe conditions and give low selectivities. The ongoing research described herein is based on the unprecedented, but thermodynamically promising, use of carbon monoxide as the oxygen atom acceptor for the catalytic deoxygenation of phenols.
- Research Organization:
- Purdue Univ., Lafayette, IN (United States). Dept. of Chemistry
- Sponsoring Organization:
- USDOE, Washington, DC (United States)
- DOE Contract Number:
- FG22-89PC89770
- OSTI ID:
- 10161810
- Report Number(s):
- DOE/PC/89770-T11; ON: DE92017307
- Resource Relation:
- Other Information: PBD: [1992]
- Country of Publication:
- United States
- Language:
- English
Similar Records
Preconversion catalytic deoxygenation of phenolic functional groups. Quarterly technial progress report, January 1, 1992--March 31, 1992
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01 COAL, LIGNITE, AND PEAT
37 INORGANIC
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PHYSICAL AND ANALYTICAL CHEMISTRY
OXYGEN COMPOUNDS
REMOVAL
CHEMICAL BONDS
CLEAVAGE
NICKEL
CATALYTIC EFFECTS
MOLYBDENUM
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ALUMINIUM OXIDES
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37 INORGANIC
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
OXYGEN COMPOUNDS
REMOVAL
CHEMICAL BONDS
CLEAVAGE
NICKEL
CATALYTIC EFFECTS
MOLYBDENUM
COBALT
IRON OXIDES
ALUMINIUM OXIDES
SILICON OXIDES
PROGRESS REPORT
PHENOLS
HYDROGENATION
THERMODYNAMICS
CARBON DIOXIDE
010402
010405
400201
PURIFICATION AND UPGRADING
HYDROGENATION AND LIQUEFACTION
CHEMICAL AND PHYSICOCHEMICAL PROPERTIES