Volume 238, 2022

Quantum resonances and roaming dynamics in formaldehyde photodissociation

Abstract

The unimolecular dissociation of formaldehyde is studied via excitation to the à band at several excitation energies from just below the ground state radical dissociation threshold to 5000 cm−1 above it. CO product rotational distributions, photofragment excitation spectroscopy and state-correlated slice imaging results are combined with quasi-classical trajectory calculations to reveal manifestations of quantum effects in this complex dissociation process involving interactions among radical, molecular, and roaming pathways. Evidence of nodal structure at the tight transition state to molecular products is investigated and correlations between the CO rotational and H2 vibrational distributions are used to suggest the transition state modes that are responsible. A large modulation of the roaming yield previously identified and associated with roaming resonances at the onset of the H + HCO(v1,v2,v3 = 0,0,0) product channel suggests a similar origin for enhanced roaming and a roaming yield that is strongly dependent on parent rotation on the 2641 band just 15 cm−1 above the H + HCO(0,2,1) threshold. Similar resonances are predicted on other bands that share near coincident energies with HCO product vibrational thresholds.

Graphical abstract: Quantum resonances and roaming dynamics in formaldehyde photodissociation

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
22 фев 2022
Accepted
24 мар 2022
First published
24 мар 2022

Faraday Discuss., 2022,238, 249-265

Author version available

Quantum resonances and roaming dynamics in formaldehyde photodissociation

C. D. Foley, C. Xie, H. Guo and A. G. Suits, Faraday Discuss., 2022, 238, 249 DOI: 10.1039/D2FD00050D

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