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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:10.1039/d6qm00041j</dc:identifier><dc:language>eng</dc:language><dc:creator>Melendo, Irene</dc:creator><dc:creator>Weatherill, Lucy A.</dc:creator><dc:creator>Martín, Antonio</dc:creator><dc:creator>Pander, Piotr</dc:creator><dc:creator>Dias, Fernando B.</dc:creator><dc:creator>Fuertes, Sara</dc:creator><dc:creator>Sicilia, Violeta</dc:creator><dc:title>Double decker NHC-cyclometallated Pt complexes for highly-efficient vacuum-deposited green OLEDs and NIR emission</dc:title><dc:identifier>ART-2026-148851</dc:identifier><dc:description>The dinuclear compound [{PtII(C^C*)(µ-N^N)}2] (HN^N: diphenylformamidine; HC^C* = 3-methyl-1-(naphthalen-2-yl)-1H-imidazol-2-ylidene, 3) was obtained as a pure single anti-isomer, with a Pt–Pt distance of 2.8645 Å. Under UV light, 3 reacted with haloforms to obtain the corresponding oxidized species [{PtIII(C^C*)(µ-N^N)X}2] (4-X). X-ray analysis of 4-Cl confirmed the retention of the anti-conformation and revealed a shortened Pt–Pt distance (2.6070 Å) consistent with metal–metal bonding in the Pt2(III,III) system. In addition, methylation of the electron-rich complex 3 with [Me3O]BF4 provided the mixed-valence dinuclear species [(C^C*)PtII(µ-N^N)2PtIV(C^C*)(CH3)]BF4 (5), which exhibits two distinct 195Pt NMR resonances (δ: −2373 and −3264 ppm) and a large Pt–Pt coupling constant (2155 Hz). Compound 3 shows a structureless emission band at 520 nm in 2 wt% PMMA (poly(methyl methacrylate)) film, with a photoluminescence decay of 1.80 µs and quantum yield of 0.90, typical of triplet metal–metal–to-ligand charge transfer (3MMLCT) [dσ*(Pt–Pt) → π*(C^C*)] excited states. The oxidized counterparts, 4-X, display phosphorescent emissions with maxima at 960, 970 and 1055 nm in solid state at 77 K. These are tentatively assigned to triplet axial ligand-to-metal–metal charge transfer (3XMMCT) [σ(X) → dσ*(Pt–Pt)]. Whilst complex 5 shows no emission in either the visible or near-infrared regions at 298 or 77 K. Organic light-emitting diodes (OLEDs) incorporating 3 as a green emitter demonstrate excellent device performance, achieving a turn-on voltage of 3 V, an external quantum efficiency (EQE) reaching 22% and a maximum luminance exceeding 22 000 cd m−2.</dc:description><dc:date>2026</dc:date><dc:source>http://zaguan.unizar.es/record/170357</dc:source><dc:doi>10.1039/d6qm00041j</dc:doi><dc:identifier>http://zaguan.unizar.es/record/170357</dc:identifier><dc:identifier>oai:zaguan.unizar.es:170357</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E17-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICIU/PID2024-155563NB-I00</dc:relation><dc:identifier.citation>Materials Chemistry Frontiers (2026), [11 pp.]</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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