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Authordc.contributor.authorHernández, Carlos T. 
Authordc.contributor.authorMorales, R. G E 
Admission datedc.date.accessioned2018-12-20T14:37:48Z
Available datedc.date.available2018-12-20T14:37:48Z
Publication datedc.date.issued1993
Cita de ítemdc.identifier.citationJournal of Physical Chemistry, Volumen 97, Issue 45, 2018, Pages 11649-11651
Identifierdc.identifier.issn00223654
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/156713
Abstractdc.description.abstractDuring the charge-transfer process in the excited state of aromatic carbonyl compounds, the local C-O net charge decreases as the polyene bridge length between the aromatic and the carbonyl systems is increased. Part of the photoinduced electronic charge, transferred through this molecular wire from the aromatic ring to the carbonyl acceptor group, is retained by the π-conduction channel of the polyene molecular wire ("bridge effect"). The present study defines the quantum molecular resistance in these polyene photoconduction channels by means of an analysis of the molecular excited states for isolated systems, based on semiempirical molecular orbital calculations (MNDO, CNDO/S). © 1993 American Chemical Society.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceJournal of Physical Chemistry
Keywordsdc.subjectPhysical and Theoretical Chemistry
Títulodc.titleBridge effect in charge-transfer photoconductiom channels. 1. Aromatic carbonyl compounds
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile