From the mass-analysed ion kinetic energy spectra of labelled ions, kinetic energy releases and thermodynamic data, it is proved that protonated n-propylbenzene (1) isomerizes into protonated isopropylbenzene (2). It is also shown that the dissociation of the less energetic metastable ions of (2), l
Photodissociation spectroscopy of (C6H6)3+: Charge localization on a dimer unit of (C6H6)3+
β Scribed by Takeshi Shibata; Kazuhiko Ohashi; Yasuhiro Nakai; Nobuyuki Nishi
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 420 KB
- Volume
- 229
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Photodissociation spectra of (C,H,):
are measured in the 700-1400 nm range. The charge resonance (CR) bands characteristic of (C,H,): are found to be kept almost intact in (C,H,)$; the spectra show the main band at z 960 nm and relatively weak one at =Z 1220 nm. The photodissociation cross section of (C,H,):
at the 960 nm band is estimated to be comparable with that of the corresponding dimer band at 920 nm. These results suggest that the charge is localized on a dimer subunit, which acts as a chromophoric core for the CR transition in (C,H,): .
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Mass-analysed ion kinetic energy spectra for collisional activation (CA) of [CSH,]+' formed via electron capture by [CSH,]" ions in collision with neutral benzene molecules have been compared for the CSH, isomers benzene, 1,5-hexedjae and 2,4-hexadiyne. Comparisons of fragment abnndPnce and total CA
## Abstract A facile synthesis of the title compounds 2 and 3 is described. The key intermediate in the synthesis, 6βdemethylβ7,7β(ethylenedioxy)β6β(phenylselenenyl)mitosane (4) was synthesized in five steps from mitomycin A. Treatment of 4 with [^14^C]methyl iodide in the presence of K~2~CO~3~ aff