Imaging and Scattering Studies of the Unimolecular Dissociation of the BrCH2CH2O Radical from BrCH2CH2ONO Photolysis at 351 nm
Author:
Affiliation:
1. The James Franck Institute and Department of Chemistry, The University of Chicago, Chicago, Illinois 60637 United States and
2. Department of Chemistry, The Ohio State University, Columbus, Ohio 43210 United States
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp4095886
Reference32 articles.
1. State‐selected photodissociation dynamics of HONO(Ã 1A‘): Characterization of the NO fragment
2. Dynamics of photodissociation of hono at 369 nm: Motional anisotropy and internal state distribution of the OH fragment
3. State‐selected photodissociation dynamics: Complete characterization of the OH fragment ejected by the HONO Ã state
4. Photodissociation of methylnitrite: State distributions, recoil velocity distribution, and alignment effects of the NO(X 2Π) photofragment
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1. CH3O Substitution Effect Revisited in the Vibrationally Resolved Laser-Induced Fluorescence Spectra of Methoxycyclohexoxy Radicals;The Journal of Physical Chemistry A;2024-02-01
2. Using reduced density matrix techniques to capture static and dynamic correlation in the energy landscape for the decomposition of the CH2CH2ONO radical and support a non-IRC pathway;The Journal of Chemical Physics;2018-07-14
3. Dissociation Pathways of the CH2CH2ONO Radical: NO2 + Ethene, NO + Oxirane, and a Non-Intrinsic Reaction Coordinate HNO + Vinoxy Pathway;The Journal of Physical Chemistry A;2016-04-28
4. Competing C–Br and O–NO Photofission upon Excitation of BrCH2CH2ONO at 193 nm;The Journal of Physical Chemistry A;2015-07-13
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