The first well resolved (I + 1 )-photodissociation spectra of molecular ions are presented. By separating the spectroscopic step (first photon) and the dissociation step (second photon) we could extend the accessible spectral region of CH,I\* and CD31+ considerably. The ions are prepared in the vibr
Spectroscopy and photodissociation of size-selected (CH3I)n+ cluster ions
β Scribed by Jack A. Syage; Jhobe Steadman
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 987 KB
- Volume
- 159
- Category
- Article
- ISSN
- 0168-1176
No coin nor oath required. For personal study only.
β¦ Synopsis
The resonant photodissociation of (CH,l)z cluster ions (n = 1-5) was studied in a crossed molecular-electron-laser beam apparatus. These results were complemented by a study of the ionization/dissociation as a function of variable energy electron ionization (EI). The fragmentation that first appears as the EI energy is raised is loss of CHj. This channel is particularly strong for n = 3. The lower energy dissociation of neutral 1, on the other hand, is essentially quenched for cluster sizes of n > 2. Intermolecular dissociation (evaporation) of CH31 was evident, but was not extensive, based on a minor sensitivity of the cluster ion distribution to El energy. The photodissociation of (CH31)i resulted in different dissociation behavior than for EL Resonant excitation of monomer CH,I' to the predissociative A electronic state gave only I + CH;. A state excitation of the cluster ions, on the other hand, resulted only in intermolecular dissociation. The photoexcitation cross-sections for the A 'E1,2 +X 2E1,2 transition are presented as a function of cluster size n. A two-photon dissociation channel is also identified and the crosssections and dissociation products are reported. Finally, the frequency resolved photofragment excitation spectra of CH31' and (CH31)i are compared.
π SIMILAR VOLUMES
The angle-velocity distribution of I(2P3/2) and I(2131/2) from photodissociation of (CH3I) n clusters was measured at 266 and 304 nm. For the monomer (n = 1), the angular distribution is very anisotropic and the translational energy spectrum is sharply peaked at high energy. For clusters (predominan
The picosecond reaction dynamics of (CHJ), clusters, initiated by A state excitation, were studied by molecular beam mass spectroscopy. Time-resolved measurements indicate that the prominent I2 and IZ(CH31)n\_2 fragments are formed within the 10 ps limit of our resolution. The cluster dynamics and g
The electronic spectrum of the hydrogen-bonded complex cation, [C,HSOH-N(CHS),]+, has been observed by trapped ion photodissociation spectroscopy, in which the yield spectrum of the product ion H+N(CHI)s was acquired for the complex ion stored in a cylindrical ion trap cell. The spectrum in the rang