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dc.contributor.authorvan Walree, Cornelius A
dc.contributor.authorvan der Wiel, Bas C
dc.contributor.authorWilliams, Rene M
dc.date.accessioned2015-11-23T05:21:57Z
dc.date.available2015-11-23T05:21:57Z
dc.date.issued2013-08-09
dc.identifier.citationvan Walree C A, van der Wiel B C & Williams RM 2013, ' Photoinduced charge transport over branched conjugation pathways: donor–acceptor substituted 1,1-diphenylethene and 2,3-diphenylbutadiene', Physical Chemistry Chemical Physics, 15(36) pp. 15234-15242.en
dc.identifier.issn1463-9076
dc.identifier.urihttp://hdl.handle.net/2328/35742
dc.descriptionThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (http://creativecommons.org/licenses/by-nc/3.0/)en
dc.description.abstractPhotoinduced charge transport in 1,1-diphenylethene and 2,3-diphenylbutadiene functionalized with an electron donating dimethylamino group and an electron accepting cyano group is reported. UV-spectroscopy reveals that in these compounds, which incorporate a cross-conjugated spacer, a direct charge transfer transition is possible. It is shown by application of the generalized Mulliken–Hush approach that introduction of an additional branching point in the π-electron spacer (i.e., when going from the 1,1-diphenylethene to the 2,3-diphenylbutadiene) leads to only a moderate reduction (68–92%) of the electronic coupling between the ground and the charge separated state. The σ-electron system is however likely to be dominant in the photoinduced charge separation process.en
dc.language.isoen
dc.publisherRoyal Society of Chemistryen
dc.rightsThis journal is © the Owner Societies 2013en
dc.titlePhotoinduced charge transport over branched conjugation pathways: donor–acceptor substituted 1,1-diphenylethene and 2,3-diphenylbutadieneen
dc.typeArticleen
dc.identifier.doihttps://doi.org/10.1039/C3CP52148Fen
dc.rights.holderthe Owner Societies 2013en
dc.rights.licenseCC-BY-NC


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