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<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:date>2018-07</dc:date>
<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>
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<dc:identifier>http://hdl.handle.net/10259/4885</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Wiley-VCH Verlag</dc:publisher>
<dc:title>Selective photooxidation of sulfides catalyzed by bis‐cyclometalated IrIII photosensitizers bearing 2,2′‐dipyridylamine‐based ligands</dc:title>
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