Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5587
DC FieldValueLanguage
dc.contributor.authorRIVADO CASAS, Len_us
dc.contributor.authorSampedro, Den_us
dc.contributor.authorCAMPOS P., Jen_us
dc.contributor.authorFusi, Stefaniaen_us
dc.contributor.authorZanirato, Ven_us
dc.contributor.authorOlivucci, Massimoen_us
dc.date.accessioned2021-03-30T15:53:41Z-
dc.date.available2021-03-30T15:53:41Z-
dc.date.issued2009-
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/5587-
dc.description38128en_US
dc.description.abstractA new family of biomimetic photoactivated molecular switches based in the retinal chromophore is described. Expedient synthesis allows a library of compounds with a different substitution pattern, including chiral substituents, to be obtained. The effect of substitution, solvent, and light source on thephotoisomerization step has been assessed. The absorption maximum has been red-shifted ca. 50 nmwith respect to related systems and rotation is now easily achieved by using visible light.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofJOURNAL OF ORGANIC CHEMISTRYen_US
dc.titleFluorenylidene-Pyrroline Biomimetic Ligth -Driven Molecular Switchesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jo802792jen_US
dc.identifier.pmid19485347en_US
dc.identifier.scopus2-s2.0-67649625273en_US
dc.identifier.isiWOS:000267432700002en_US
dc.relation.volume74en_US
dc.relation.issue13en_US
dc.description.firstpage4666en_US
dc.description.lastpage4674en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0003-1792-902X-
crisitem.author.orcid0000-0002-8247-209X-
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