Affiliation:
1. Department of Chemistry, University of Ottawa, 10 Marie-Curie, Ottawa, ON K1N 6N5, Canada.
Abstract
A commercial analytical mass spectrometer coupled with a spectrograph and charge-coupled device (CCD) detector was used to obtain the collision-induced emission (CIE) spectra (190–1020 nm) from ion–molecule collisions between N2O+•and He at laboratory frame collision energies of 4–8 keV. The observed emissions were from the A2Σ+ → X2Π+system of N2O+•, excited fragments of the parent molecule, and the target gas. The relative emission intensities of the N2O+•ions and their fragments were independent of the ion translational energy within the 4–8 keV range, confirming the curve-crossing mechanism for translational-to-internal energy transfer in this system. Band emission intensities of [Formula: see text] and [Formula: see text] relative to the [Formula: see text] band within the N2O+•(A → X) system have been measured and compared with reference data. The results indicated that the collisionally excited ion has a decidedly non-Franck–Condon vibrational state distribution.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
1 articles.
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