<?xml version="1.0" encoding="UTF-8"?>
<collection>
<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:10.3390/inorganics12100271</dc:identifier><dc:language>eng</dc:language><dc:creator>Martínez, Miguel</dc:creator><dc:creator>Dalmau, David</dc:creator><dc:creator>Crespo, Olga</dc:creator><dc:creator>García-Orduña, Pilar</dc:creator><dc:creator>Lahoz, Fernando</dc:creator><dc:creator>Martín, Antonio</dc:creator><dc:creator>Urriolabeitia, Esteban P.</dc:creator><dc:title>Different Patterns of Pd-Promoted C-H Bond Activation in (Z)-4-Hetarylidene-5(4H)-oxazolones and Consequences in Photophysical Properties</dc:title><dc:identifier>ART-2024-140555</dc:identifier><dc:description>This work aims to amplify the fluorescence of (Z)-4-hetarylidene-5(4H)-oxazolones 1 by suppression of the hula-twist non-radiative deactivation pathway by C^N-orthopalladation of the 4-hetarylidene ring. Different (Z)-4-hetarylidene-2-phenyl-5(4H)-oxazolones, 1a–1c, prepared by the Erlenmeyer–Plöchl method, have been studied. The orthopalladation of (Z)-2-phenyl-4-(5-thiazolylmethylene)-5(4H)-oxazolone (1a) takes place by C-H bond activation of the H4 of the heterocycle and C^N-chelation, giving the dinuclear trifluoroacetate derivative 2a. By further metathesis of bridging ligands in 2a, complexes containing the orthometalated oxazolone and a variety of ligands 3a–5a, were prepared. The study of the photophysical properties of 1a–5a shows that the bonding of the Pd metal to the 4-hetaryliden-5(4H)-oxazolone does not promote, in these cases, an increase in fluorescence. Interestingly, the orthopalladation of (Z)-2-phenyl-4-(4-thiazolylmethylene)-5(4H)-oxazolone (1b) gives orthopalladated 2b, where the incorporation of the Pd to the oxazolone takes place by C-H bond activation of the ortho-H2 of the 2-phenyl group, ring opening of the oxazolone heterocycle and simultaneous N,N-bonding of the N atoms of the thiazole ring and the generated benzamide fragment. This N^N^C-tridentate dianionic bonding mode is obtained for the first time in oxazolones. Despite a similar lock of the hula-twist deactivation, 2b does not show fluorescence.</dc:description><dc:date>2024</dc:date><dc:source>http://zaguan.unizar.es/record/145634</dc:source><dc:doi>10.3390/inorganics12100271</dc:doi><dc:identifier>http://zaguan.unizar.es/record/145634</dc:identifier><dc:identifier>oai:zaguan.unizar.es:145634</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E07-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E17-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN AEI/PID2022-136861NB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2019-106394GB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2021-122869NB-I00</dc:relation><dc:identifier.citation>Inorganics 12, 10 (2024), 271 [16 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>https://creativecommons.org/licenses/by/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>