Examination of the Orientation of the Angular Momentum of the NO Photofragment from the 280 nm. Photodissociation of Methyl Nitrite Using Circularly Polarized Light

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Authors
Klobuchar, Aidan James
Issue Date
2011
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Thesis
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en_US
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Abstract
Methyl nitrite is a highly studied molecule for investigation of the photodissociation dynamics of a bent system. While our lab has previously studied the vector correlations in the 225 nm photodissociation of CH3ONO, reveal- ing the alignment of the j, v and vectors, the orientation of these vectors has not yet been measured. The goal of the investigation was to discover the orientation of the j vector to determine whether the O-N-O bond angle increased or decreased during the dissociation event using the 2 0(21) odd bipolar moment. A three color photodissociation and 1 + 10 REMPI scheme was used for photodissociation and ionization: 280 nm linearly polarized light for dissociation of CH3ONO, a tunable 223 - 226 nm circularly polar- ized beam to probe the NO, and a 308 nm beam for ionizing excited NO. The NO+ product ions were detected by photofragment ion imaging. The ion images were analyzed in order to determine the value of the 2 0(21) odd bipolar moment. For P and R branch transitions, the ion images showed a qualitative dependence on the helicity of the circularly polarized light and produced average values of 2 0(21) of 􀀀0:40 and 􀀀0:23 for P and R (P11 and Q21 + R11) branches respectively. As expected, the Q branches showed no signi cant dependence on the helicity of the probe light. This indicates that the O-N-O bond angle increases on the excited surface. This is in contrast to NO2, which has been shown to have the O-N-O bond angle decrease as the dissociation event unfolds.
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viii, 44 p.
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Kalamazoo College
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U.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder. All rights reserved.
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