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How important is roaming in the photodegradation of nitrobenzene?

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How important is roaming in the photodegradation of nitrobenzene?

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dc.contributor.author Giussani, Angelo
dc.contributor.author Worth, Graham A.
dc.date.accessioned 2023-02-08T15:15:35Z
dc.date.available 2023-02-08T15:15:35Z
dc.date.issued 2020
dc.identifier.citation Giussani, Angelo Worth, Graham A. 2020 How important is roaming in the photodegradation of nitrobenzene? Physical Chemistry Chemical Physics 22 15945 15952
dc.identifier.uri https://hdl.handle.net/10550/85357
dc.description.abstract At low excitation energies nitrobenzene photoreleases NO with low translational and rotational energy, while at higher excitation energies NO is photoreleased with both low and high translational and rotational energy. The fast products are formed through a singlet-triplet crossing (STC) region featuring an oxaziridine ring, while a ground state roaming mechanism was suggested to produce the slow molecules. Computing translational and rotational energies performing CASSCF classical dynamics, we here prove how the same oxaziridine STC can account for both fast and slow photoproducts, depending on the region of the seam through which the ground state is populated. A roaming-type STC/CI has also been characterized, from which slow NO molecules can also be formed through a roaming photodegradation mechanism, here in the excited state. The higher accessibility of the oxaziridine STC mechanism, 1.53 eV lower in energy than the roaming path, questions the contribution of roaming in nitrobenzene NO photoproduction.
dc.language.iso eng
dc.relation.ispartof Physical Chemistry Chemical Physics, 2020, vol. 22, p. 15945-15952
dc.subject Fisicoquímica
dc.subject Energia
dc.title How important is roaming in the photodegradation of nitrobenzene?
dc.type journal article es_ES
dc.date.updated 2023-02-08T15:15:35Z
dc.identifier.doi 10.1039/D0CP02077J
dc.identifier.idgrec 144464
dc.rights.accessRights open access es_ES

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