Giuliani, A.; Walker, I.C.; Delwiche, J.; Hoffmann, S.V.; Limao-Viera, P.; Mason, N.J.; Heyne, B.; Hoebeke, M. and Hubin-Franskin, M.J.
(2003).
| DOI (Digital Object Identifier) Link: | https://doi.org/10.1063/1.1603733 |
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| Google Scholar: | Look up in Google Scholar |
Abstract
The photoelectron spectrum of 2-furanmethanol (furfuryl alcohol) has been measured for ionization energies between 8 and 11.2 eV and the first three ionization bands assigned to π3,π2, and no ionizations in order of increasing binding energy. The photoabsorption spectrum has been recorded in the gas phase using both a synchrotron radiation source (5–9.91 eV, 248–125 nm) and electron energy-loss spectroscopy under electric-dipole conditions (5–10.9 eV, 248–90 nm). The (UV) absorption spectrum has also been recorded in solution (4.2–6.36 eV, 292–195 nm). The electronic excitation spectrum appears to be dominated by transitions between π and π* orbitals in the aromatic ring, leading to the conclusion that the frontier molecular orbitals of furan are affected only slightly on replacement of a H atom by the –CH2OH group. Additional experiments investigating electron impact at near-threshold energies have revealed two low-lying triplet states and at least one electron/molecule shape resonance. Dissociative electron attachment also shows to be widespread in furfuryl alcohol.
| Item Type: | Article |
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| ISSN: | 0021-9606 |
| Extra Information: | Some of the symbols may not have transferred correctly into this bibliographic record. |
| Academic Unit/School: | Faculty of Science, Technology, Engineering and Mathematics (STEM) > Physical Sciences Faculty of Science, Technology, Engineering and Mathematics (STEM) |
| Interdisciplinary Research Centre: | Centre for Earth, Planetary, Space and Astronomical Research (CEPSAR) |
| Item ID: | 4870 |
| Depositing User: | Users 6041 not found. |
| Date Deposited: | 17 Jul 2006 |
| Last Modified: | 29 Nov 2016 16:55 |
| URI: | http://oro.open.ac.uk/id/eprint/4870 |
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