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oai:riubu.ubu.es:10259/49392021-11-10T09:38:18Zcom_10259_3844com_10259_5086com_10259_2604col_10259_3845

Martínez Alonso, Marta Cerdá, Jesús . Momblona, Cristina . Pertegás, Antonio . Junquera Hernández, José M. . Heras, Aránzazu Rodríguez, Ana M. . Espino Ordóñez, Gustavo Bolink, Henk . Ortí, Enrique . A series of bis-cyclometalated iridium(III) complexes of general formula [Ir(ppy)2(N∧N)][PF6] (ppy− = 2-phenylpyridinate; N∧N = 2-(1H-imidazol-2-yl)pyridine (1), 2-(2-pyridyl)benzimidazole (2), 1-methyl-2-pyridin-2-yl- 1H-benzimidazole (3), 2-(4′-thiazolyl)benzimidazole (4), 1- methyl-2-(4′-thiazolyl)benzimidazole (5)) is reported, and their use as electroluminescent materials in light-emitting electrochemical cell (LEC) devices is investigated. [2][PF6] and [3][PF6] are orange emitters with intense unstructured emission around 590 nm in acetonitrile solution. [1][PF6], [4][PF6], and [5][PF6] are green weak emitters with structured emission bands peaking around 500 nm. The different photophysical properties are due to the effect that the chemical structure of the ancillary ligand has on the nature of the emitting triplet state. Whereas the benzimidazole unit stabilizes the LUMO and gives rise to a 3MLCT/3LLCT emitting triplet in [2][PF6] and [3][PF6], the presence of the thiazolyl ring produces the opposite effect in [4][PF6] and [5][PF6] and the emitting state has a predominant 3LC character. Complexes with 3MLCT/3LLCT emitting triplets give rise to LEC devices with luminance values 1 order higher than those of complexes with 3LC emitting states. Protecting the imidazole N−H bond with a methyl group, as in complexes [3][PF6] and [5][PF6], shows that the emissive properties become more stable. [3][PF6] leads to outstanding LECs with simultaneously high luminance (904 cd m−2), efficiency (9.15 cd A−1), and stability (lifetime over 2500 h). 2018-09-12 2018-09-12 2017-09 info:eu-repo/semantics/article 0020-1669 http://hdl.handle.net/10259/4939 10.1021/acs.inorgchem.7b01167 eng Inorganic Chemistry. 2017, V. 56, n. 17, p. 10298–10310 https://doi.org/10.1021/acs.inorgchem.7b01167 info:eu-repo/grantAgreement/MINECO/CTQ2014-58812-C2-1-R info:eu-repo/grantAgreement/MINECO/MAT2014-55200 info:eu-repo/grantAgreement/MINECO/CTQ2014-55583-R info:eu-repo/grantAgreement/MINECO/CTQ2014-61914-EXP info:eu-repo/grantAgreement/MINECO/CTQ2015-71955-REDT info:eu-repo/grantAgreement/MINECO/CTQ2015- 70371-REDT info:eu-repo/grantAgreement/MINECO/CTQ2015-71154-P info:eu-repo/grantAgreement/MICINN/MDM-2015-0538 info:eu-repo/grantAgreement/FEDER/CTQ2015-71154-P info:eu-repo/grantAgreement/FundaciónLaCaixa/OSLC-2012-007 info:eu-repo/grantAgreement/JCyL/BU033-U16 info:eu-repo/grantAgreement/GVA/Prometeo2016-135 info:eu-repo/semantics/openAccess American Chemical Society