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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1021/acs.joc.0c02438</dc:identifier><dc:language>eng</dc:language><dc:creator>Tejeda-Orusco, V.</dc:creator><dc:creator>Andreu, R.</dc:creator><dc:creator>Orduna, J.</dc:creator><dc:creator>Villacampa, B.</dc:creator><dc:creator>Franco, S.</dc:creator><dc:creator>Civera, A.</dc:creator><dc:title>Twisted One-Dimensional Charge Transfer and Related Y-Shaped Chromophores with a 4 H-Pyranylidene Donor: Synthesis and Optical Properties</dc:title><dc:identifier>ART-2021-123284</dc:identifier><dc:description>Three series of push-pull derivatives bearing 4H-pyranylidene as electron donor group and a variety of acceptors were designed. On one hand, one-dimensional chromophores with a thiophene ring (series 1H) or 5-dimethylaminothiophene moiety (series 1N) as an auxiliary donor, non-coplanar with the p-conjugated system, were synthesized. On the other hand, related two-dimensional (2D) Y-shaped chromophores (series 2) were also prepared to compare how the diverse architectures affect the electrochemical, linear, and second-order nonlinear optical (NLO) properties. The presence of the 5-dimethylaminothiophene moiety in the exocyclic C= C bond of the pyranylidene unit gives rise to oxidation potentials rarely low, and the protonation (with an excess of trifluoroacetic acid) of its derivatives results in the apparition of a new blue-shifted band in the UV-visible spectra. The analysis of the properties of derivatives with and without the additional thiophene ring shows that this auxiliary donor leads to a higher NLO response, accompanied by an enhanced transparency. Y-shaped chromophores of series 2 present a blue-shifted absorption, higher molar extinction coefficients, and higher Eox values compared to their linear twisted counterparts. As concerns NLO properties, 2D Y-shaped architecture gives rise to somewhat lower µß values (except for thiobarbiturate derivatives).</dc:description><dc:date>2021</dc:date><dc:source>http://zaguan.unizar.es/record/109589</dc:source><dc:doi>10.1021/acs.joc.0c02438</dc:doi><dc:identifier>http://zaguan.unizar.es/record/109589</dc:identifier><dc:identifier>oai:zaguan.unizar.es:109589</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FEDER-FSE 2014–2020/E14-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2019-104307GB-I00-AEI-10.13039-501100011033</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/UZ/UZ2019-CIE-01</dc:relation><dc:identifier.citation>Journal of Organic Chemistry 86 (2021), 3152-3163</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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