<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-26T10:35:40Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/97645" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/97645</identifier><datestamp>2025-09-05T18:26:22Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Fernández-Hernández, Jesús M.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Beltrán Fínez, Juan Ignacio</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Lemaur, Vicent</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Gálvez-López, María-Dolores</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Chien, Chen-Han</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Polo, Federico</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Orselli, Enrico</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Fröhlich, Roland</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Cornil, Jérôme</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>De Cola, Luisa</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2024-02-01T12:11:24Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2024-02-01T12:11:24Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2013</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Fernandez-Hernandez, J. M., Beltran, J. I., Lemaur, V., Galvez-Lopez, M. D., Chien, C. H., Polo, F., ... &amp; De Cola, L. (2013). Iridium (III) Emitters Based on 1, 4-Disubstituted-1 H-1, 2, 3-triazoles as Cyclometalating Ligand: Synthesis, Characterization, and Electroluminescent Devices. Inorganic Chemistry, 52(4), 1812-1824.</mods:identifier>
   <mods:identifier type="issn">0020-1669</mods:identifier>
   <mods:identifier type="doi">10.1021/ic3018419</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/97645</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.1021/ic3018419</mods:identifier>
   <mods:abstract>A series of blue and blue-green emitters based on neutral bis- and tris-cyclometalated Ir(III) complexes with 1-benzyl-4-(2,6-difluorophenyl)-1H-1,2,3-triazole (dfptrBn) as cyclometalating ligand is reported. The bis-cyclometalated complexes of the type [Ir(dfptrBn)(2)((LX)-X-boolean AND)] with different ancillary ligands, (LX)-X-boolean AND = picolinate (pic) (2) or 2-(5-(perfluorophenyl)-2H-1,2,4-triazol-3-yl)pyridine (pytrF(5)) (3), are described and their photophysical properties compared with the analogous complexes containing the archetypal 2-(2,4-difluorophenyl)-pyridinato (dfppy) as cyclometaled ligand ((CN)-N-boolean AND). Complex 2 exhibits a marked solvatochromic behavior, from 475 nm in toluene to 534 nm in formamide, due to the strong MLCT character of its emissive excited state. Complex 3 displays a true-blue emission, narrower in the visible part than FIrpic. In addition, the homoleptic complex [Ir(dfprBn)(3)] (4) and the heteroleptic compounds with mixed arylpyridine/aryltriazole ligands, [Ir(dfptrBn)(2)((CN)-N-boolean AND)] ((CN)-N-boolean AND = 2-phenylpyridinato (ppy) (5) or dfppy (6)), have been synthesized and fully characterized. The facial (fac) complex fac-4 is emissive at 77 K showing a deep-blue emission, but it is not luminescent in solution at room temperature similarly to their phenylpyrazole counterparts. However, the fac isomers, fac-5 and fac-6, are highly emissive in solution and thin films, reaching emission quantum yields of 76%, with emission colors in the blue to blue-green region. The photophysical properties for all complexes have been rationalized by means of quantum-chemical calculations. In addition, we constructed electroluminescent devices, organic light-emitting diodes (OLEDs) by sublimation of fac-6, and by solution processed polymer-based devices (PLEDs) using complexes fac-5 or fac-6 as dopants.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Iridium(III) emitters based on 1,4-disubstituted-1H-1,2,3-triazoles as cyclometalating ligand: synthesis, characterization, and electroluminescent devices</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods></metadata></record></GetRecord></OAI-PMH>