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Article: Electron transfer rates from vibrational quantum states

TitleElectron transfer rates from vibrational quantum states
Authors
Issue Date1996
Citation
Journal of Physical Chemistry, 1996, v. 100, n. 24, p. 10206-10209 How to Cite?
AbstractElectron transfer involves changes in molecular geometry that are important for controlling rates. In this work we report the first clear effects of vibrational quantum state on solution phase electron transfer rates. The spontaneous electron transfer rates for the recovery of an ion pair [Co(Cp)2+/V(CO)6-] are studied with picosecond infrared spectroscopy following optical excitation into its charge transfer band. The rates increase about 2-fold for each additional vibrational quantum in the CO stretching mode. These results allow new tests of electron transfer theory. © 1996 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/346528
ISSN

 

DC FieldValueLanguage
dc.contributor.authorSpears, Kenneth G.-
dc.contributor.authorWen, Xiaoning-
dc.contributor.authorZhang, Ruihua-
dc.date.accessioned2024-09-17T04:11:31Z-
dc.date.available2024-09-17T04:11:31Z-
dc.date.issued1996-
dc.identifier.citationJournal of Physical Chemistry, 1996, v. 100, n. 24, p. 10206-10209-
dc.identifier.issn0022-3654-
dc.identifier.urihttp://hdl.handle.net/10722/346528-
dc.description.abstractElectron transfer involves changes in molecular geometry that are important for controlling rates. In this work we report the first clear effects of vibrational quantum state on solution phase electron transfer rates. The spontaneous electron transfer rates for the recovery of an ion pair [Co(Cp)2+/V(CO)6-] are studied with picosecond infrared spectroscopy following optical excitation into its charge transfer band. The rates increase about 2-fold for each additional vibrational quantum in the CO stretching mode. These results allow new tests of electron transfer theory. © 1996 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of Physical Chemistry-
dc.titleElectron transfer rates from vibrational quantum states-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jp960444a-
dc.identifier.scopuseid_2-s2.0-0000100811-
dc.identifier.volume100-
dc.identifier.issue24-
dc.identifier.spage10206-
dc.identifier.epage10209-

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