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Title: | New NHC cycloplatinated compounds. Significance of the cyclometalated group on the electronic and emitting properties of bis-cyanide compounds |
Authors: | Fuertes, Sara CSIC ORCID; Chueca, Andrés J.; Martín, Antonio CSIC ORCID; Sicilia, Violeta CSIC ORCID | Keywords: | Cyclometalated NHC Cyanide Organometallic compounds Luminescence |
Issue Date: | 1-Jul-2019 | Publisher: | Elsevier | Citation: | Journal of Organometallic Chemistry 889: 53-61 (2019) | Abstract: | Compounds NBu[Pt(CˆC*)(CN)] (HCˆC* = 1-(4-(ethoxycarbonyl)phenyl)-3-methyl-1H-imidazol-2-ylidene 1, HCˆC* = 1-(4-cyanophenyl)-3-methyl-1H-imidazol-2-ylidene 2, HCˆC* = 1-(3,5-dichlorophenyl)-3-methyl-1H-imidazol-2-ylidene 3) and NBu [Pt(CˆC*)(CN)] (1′-3′) were synthesized by addition of KCN (or KCN) to freshly prepared species [Pt(CˆC*)(NCCH)]ClO, in a 2:1 M ratio. Single crystal X-ray structures of 1–3 showed the absence of intermolecular π-π and Pt-Pt interactions. The Pt{H} NMR data of 1–3 were obtained and compared with those of the related compounds NBu[Pt(CˆN)(CN)] (CˆN = benzoquinolate, bzq; phenylpyridinate, ppy). They indicate that the electronic density on the Pt center is larger for NBu[Pt(CˆC*)(CN)](1–3) than for NBu[Pt(CˆN)(CN)], which has been proved through NBO charge distribution analysis. Compounds 1 and 2 resulted to be rather good blue-emitters with their emissions arising mainly from IL [π(NHC) → π*(NHC)] excited states with little MLCT [5d(Pt) → π*(NHC)] character. The emission of 2 in PMMA film render PLQY (Ф) of 70% and Commission Internationale de L'Eclairage (CIE) coordinates (0.15, 0.19) highly close to the optimal ones for blue emitters (0.15, 0.15). | Publisher version (URL): | http://doi.org/10.1016/j.jorganchem.2019.03.012 | URI: | http://hdl.handle.net/10261/208542 | DOI: | 10.1016/j.jorganchem.2019.03.012 | Identifiers: | doi: 10.1016/j.jorganchem.2019.03.012 issn: 0022-328X |
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