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Reactivity Trends in Furan and Alkyl Furan Combustion
Energy & Fuels, 2014A systematic study of the ignition behavior of furan and the substituted furans 2-methyl furan (2-MF) and 2,5-dimethyl furan (DMF) is presented. Ignition delay times are measured over a temperature range from 977 to 1570 K and pressures up to 12 atm for lean, stoichiometric, and rich mixtures of fuel, oxygen, and argon.
Mazen A. Eldeeb, Benjamin Akih-Kumgeh
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The Electronic Spectrum of Furan
Journal of the American Chemical Society, 1998The 30 lowest electronic states of furan have been investigated with theoretical calculations (up to approximately 8.3 eV), and the experimental spectrum scrutinized in the relevant energy region.
Christiansen, O., Jørgensen, Poul
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The Conversion of Furans into Phosphinines
Chemistry – A European Journal, 2011AbstractThe [4+2] cycloadducts between furan compounds and a methylenechlorophosphane pentacarbonyltungsten complex are converted into the corresponding 2‐hydroxy‐ or 2‐bromophosphinine complexes by treatment with BBr3 and triethylamine. The X‐ray crystal structure of the parent 2‐phosphaphenol complex shows that the hydroxy substituent is coplanar ...
Yanli, Mao, François, Mathey
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Electron collisions with furan
The Journal of Chemical Physics, 2007The authors report integral, differential and momentum transfer cross sections for elastic scattering of low-energy electrons by C4H4O (furan) molecules. Their calculations employed the Schwinger multichannel method with pseudopotentials and were performed in the static-exchange and in the static-exchange plus polarization approximations.
M H F, Bettega, M A P, Lima
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Organic Letters, 2010
The reaction between methylenechlorophosphine-pentacarbonyltungsten and furan affords a [4 + 2] adduct whose oxygen bridge is broken by BBr(3), leading to a 2-alkoxyphosphinine after two additional steps.
Yanli, Mao, Francois, Mathey
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The reaction between methylenechlorophosphine-pentacarbonyltungsten and furan affords a [4 + 2] adduct whose oxygen bridge is broken by BBr(3), leading to a 2-alkoxyphosphinine after two additional steps.
Yanli, Mao, Francois, Mathey
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FURAN REACTIONS. I. THE PYROLYSIS OF FURAN
Journal of the American Chemical Society, 1932Charles D. Hurd, A. R. Goldsby
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