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<dc:title>Selective photooxidation of sulfides catalyzed by bis‐cyclometalated IrIII photosensitizers bearing 2,2′‐dipyridylamine‐based ligands</dc:title>
<dc:creator>Vaquero Gutiérrez, Mónica</dc:creator>
<dc:creator>Ruiz Riaguas, Alba</dc:creator>
<dc:creator>Martínez Alonso, Marta</dc:creator>
<dc:creator>Jalón Sotés, Félix Ángel</dc:creator>
<dc:creator>Manzano, Blanca R. .</dc:creator>
<dc:creator>Rodríguez, Ana M. .</dc:creator>
<dc:creator>García Herbosa, Gabriel</dc:creator>
<dc:creator>Carbayo Martín, Mª Aránzazu</dc:creator>
<dc:creator>García Ruiz, Begoña</dc:creator>
<dc:creator>Espino Ordóñez, Gustavo</dc:creator>
<dc:subject>Química</dc:subject>
<dc:subject>Chemistry</dc:subject>
<dc:description>A new family of heteroleptic bis-cyclometalated IrIII&#xd;
complexes with formula [Ir(C&#xd;
_&#xd;
N)2(N&#xd;
_&#xd;
N)]Cl (C&#xd;
_&#xd;
N=2-phenylpyridinate&#xd;
and N&#xd;
_&#xd;
N=2,2’-dipyridylamine or N-benzylated 2,2’-dipyridylamines,&#xd;
were synthesized, characterized, and successfully&#xd;
used as photosensitizers in the catalytic photooxidation of&#xd;
an array of dialkyl, dibenzyl, alkyl aryl, and diaryl sulfides, as&#xd;
well as sulfur-containing amino acids. Furthermore, the reactions&#xd;
proceeded with optimal chemoselectivity, and atom&#xd;
economy under mild conditions. Experimental observations&#xd;
support a dual mechanism in which singlet oxygen and superoxide&#xd;
are the actual oxidants.</dc:description>
<dc:description>Consejer&#xd;
&amp;a de Educacijn-Junta de Castilla y Lejn (BU042U16). Financial&#xd;
support by the Spanish Ministry of Economy and Competitiveness&#xd;
(MINECO) (projects CTQ2014-58812-C2@1-R,&#xd;
(CTQ2014-58812-C2-2-R, CTQ2015-70371-REDT, FEDER funds),&#xd;
Obra Social “la Caixa” (OSLC-2012-007), Junta de Castilla y Lejn&#xd;
(BU-042U16)</dc:description>
<dc:date>2018-08-27T08:18:09Z</dc:date>
<dc:date>2019-07-25T02:45:07Z</dc:date>
<dc:date>2018-07</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
<dc:identifier>0947-6539</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4885</dc:identifier>
<dc:identifier>10.1002/chem.201801173</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Chemistry-a european journal. 2018, V. 24, n. 42, p. 10662-10671</dc:relation>
<dc:relation>https://doi.org/10.1002/chem.201801173</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU042U16</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2014-58812-C2-1-R</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2014-58812-C2-2-R</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2015-70371-REDT</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/FundaciónLaCaixa/OSLC-2012-007</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Wiley-VCH Verlag</dc:publisher>
<europeana:object>https://riubu.ubu.es/bitstream/10259/4885/4/Vaquero-Chemistry_2018.pdf.jpg</europeana:object>
<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://rightsstatements.org/vocab/CNE/1.0/</europeana:rights>
<europeana:dataProvider>RIUBU. Repositorio Institucional de la Universidad de Burgos</europeana:dataProvider>
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