Infrared photodissociation of small methanol clusters
โ Scribed by Friedrich Huisken; Martin Stemmler
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 468 KB
- Volume
- 144
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
A continuous supersonic molecular beam of small methanol clusters is crossed by the radiation of a pulsed CO2 laser. Subsequent scattering by a secondary He beam disperses the cluster beam and allows the off-axis detection of selected cluster species, undisturbed by ionizer fragmentation artifacts. In the region of the yg C-O stretching vibration, the dependence of IR photon absorption on laser frequency and fluence is investigated as a function of cluster size. The predissoeiation spectrum of the dimer shows two distinct peaks at 1026.5 and 1051.6 cm-' which correspond to the excitation of the two non-equivalent monomers in the dimer. The trimer spectrum features one single peak centered at 1042.2 cm-'. This is consistent with a cyclic structure in which all three methanol molecules are equivalent. Higher cluster spectra are characterized by single peaks gradually blue-shifted with respect to the trimer line.
๐ SIMILAR VOLUMES
Photodissociation spectra of (N,H,), clusters from the dimer to the hexamer have been measured near the monomer frequencies of the v,~ mode at 937 cm-' (NH2 wag) and the u5 mode at 1098 cm-' (N-N stretch). The clusters are size-selected by the combination of a scattering process with a He beam and a
The infrared photodissociation of mass selected cluster-adsorbate complexes Au~-(CH3OH) m (m = 1-3) is studied in a Penning ion trap. Spectra are obtained by the excitation of vibrational modes of methanol, the desorption of neutral molecules and the detection of fragment ions by time-of-flight mass