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- W1967703011 abstract "A comparison was made between the mass spectra of propane (CH3CH2CH3) for resonant soft X-ray photofragmentation and for electron-impact ionization. The soft X-ray photon energy was tuned to 287.7 eV to promote Auger relaxations from the C–H bonds (1s→C–H σ∗ transition). It was hypothesized that this would lead to proton loss without C–C chain fragmentation. Compared to traditional 70 eV electron-impact ionization, photoionization does bias the mass spectrum toward proton loss; however, residual vibrational energy in the room temperature propane leads to a non-trivial amount of C–C bond scission. The resonant soft X-ray photofragmentation is dominated by three-carbon ions between 38 and 40 u created by the loss of hydrogen while the electron-impact ionization is dominated by a major peak at 29 u corresponding to the two-carbon ion C2H5+. Within each envelope of three-, two-, or single-carbon ions the core-level photoionization spectrum showed a bias toward enhanced multiple hydrogen removal compared to the electron-stimulated spectrum." @default.
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- W1967703011 date "2003-07-01" @default.
- W1967703011 modified "2023-09-23" @default.
- W1967703011 title "Resonant soft X-ray photofragmentation of propane" @default.
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- W1967703011 doi "https://doi.org/10.1016/s0368-2048(03)00053-7" @default.
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