The use of photoelectron angular distributions to provide structural details of cluster environments is investigated. Photoelectron spectra and angular distributions of I(-)·(H2O)2 and I(-)·(CH3CN)2 cluster anions are recorded over a range of photon energies. The anisotropy parameter (β) for electrons undergoes a sharp change (Δβmax) at photon energies close to a detachment channel threshold.
View Article and Find Full Text PDFA photodissociative study of CuO2(-) is presented using a combination of energy and time domain photoelectron spectroscopy. Ion source conditions are used that solely produce linear OCuO(-). Photodissociation of this isomer to produce Cu(-) + O2 is conclusively demonstrated at wavelengths between 765 and 340 nm.
View Article and Find Full Text PDFPhotoelectron imaging results are presented for I(-)[middle dot]X cluster anions (X = CO(2), C(4)H(5)N [pyrrole], (CH(3))(2)CO, CH(3)NO(2)). The available detachment channels are labeled according to the neutral iodine atom states produced (channel I ≡ (2)P(3/2) and channel II ≡ (2)P(1/2)). At photon energies in the vicinity of the channel II threshold these data are compared to previously reported results for I(-)[middle dot]X (X = CH(3)CN, CH(3)Cl, CH(3)Br, and H(2)O).
View Article and Find Full Text PDFWe present the results of a photoelectron imaging study of the I(-)·(CH(3)I)(2) cluster anion over excitation wavelengths 355-260 nm. The resulting spectra and photoelectron angular distributions (PADs) suggest extensive electron-molecule interaction following photoexcitation. Fragmentation channels are observed subsequent to excitation between 355 and 330 nm.
View Article and Find Full Text PDFCl(-)·CH(3)I cluster anion photoelectron images are recorded over a range of detachment wavelengths in the immediate post threshold region. The photoelectron spectral features fall into two categories. A number of weak, photon energy dependent transitions are observed and attributed to atomic anion fragmentation products.
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