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El texto completo de este trabajo no se encuentra disponible por no haber sido facilitado aún por su autor, por restricciones de copyright, o por no existir una versión digital, Neutral green-emitting four-coordinate Cu(I) complexes with general formula POPCu(NN), where POP = bis[2-(diphenylphosphino)phenyl]ether and NN = substituted 2-pyridine-1,2,4-triazole ligands, were synthesized. The crystal structures of (POPCuMeCN)+(PF6)− (1), POPCuPhPtp (2a, PhPtp = 2-(5-phenyl-2H-[1,2,4]triazol-3-yl)-pyridine), and POPCu(3,5-2FPhPtp) (2d, 3,5-2FPhPtp = 2-(5-(3,5-difluorophenyl)-2H-1,2,4-triazol-3-yl)pyridine) were determined by single-crystal X-ray diffraction analysis. The electronic and photophysical properties of the complexes were examined by UV–vis, steady-state, and time-resolved spectroscopy. At room temperature, weak emission was observed in solution, while in the solid state, all complexes exhibit intense green emission with quantum yield up to 0.54. The electronic and photophysical properties were further supported by calculation performed at the (time-dependent) density functional theory level. One of the complexes was also tested as dopant in electroluminescent devices., National Basic Research Program of China, National Natural Science Foundation of China (NSFC), Jiangsu Fund for Distinguished Young Scientist, Jiangsu Specially-Appointed Professor Program, Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), Jiangsu Scientist and Technological Innovation Team, Natural Science Foundation of Jiangsu Province, China Postdoctoral Science Foundation, Specialized Research Fund for the Doctoral Program of Higher Education (SRFDP), Region Wallonne (OPTI2MAT excellence program), European Community, Depto. de Física de Materiales, Fac. de Ciencias Físicas, TRUE, pub

Esta depositada la versión del artículo enviada a la revista, 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., Fundacion Seneca, Instituto de Salud Carlos III, Ministry of Science and Technology, Taiwan, Deutscher Akademischer Austausch Dienst (DAAD), Fonds de la Recherche Scientifique - FNRS, Ministerio de Ciencia e Innovación (España), Depto. de Física de Materiales, Fac. de Ciencias Físicas, TRUE, pub

El texto completo de este trabajo no se encuentra disponible por no haber sido facilitado aún por su autor, por restricciones de copyright, o por no existir una versión digital, Neutral green-emitting four-coordinate Cu(I) complexes with general formula POPCu(NN), where POP = bis[2-(diphenylphosphino)phenyl]ether and NN = substituted 2-pyridine-1,2,4-triazole ligands, were synthesized. The crystal structures of (POPCuMeCN)+(PF6)− (1), POPCuPhPtp (2a, PhPtp = 2-(5-phenyl-2H-[1,2,4]triazol-3-yl)-pyridine), and POPCu(3,5-2FPhPtp) (2d, 3,5-2FPhPtp = 2-(5-(3,5-difluorophenyl)-2H-1,2,4-triazol-3-yl)pyridine) were determined by single-crystal X-ray diffraction analysis. The electronic and photophysical properties of the complexes were examined by UV–vis, steady-state, and time-resolved spectroscopy. At room temperature, weak emission was observed in solution, while in the solid state, all complexes exhibit intense green emission with quantum yield up to 0.54. The electronic and photophysical properties were further supported by calculation performed at the (time-dependent) density functional theory level. One of the complexes was also tested as dopant in electroluminescent devices., National Basic Research Program of China, National Natural Science Foundation of China (NSFC), Jiangsu Fund for Distinguished Young Scientist, Jiangsu Specially-Appointed Professor Program, Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), Jiangsu Scientist and Technological Innovation Team, Natural Science Foundation of Jiangsu Province, China Postdoctoral Science Foundation, Specialized Research Fund for the Doctoral Program of Higher Education (SRFDP), Region Wallonne (OPTI2MAT excellence program), European Community, Depto. de Física de Materiales, Fac. de Ciencias Físicas, TRUE, pub

From a series of bis(alkynyl)mesityl phosphanes 5, we prepared phosphirenium borate compounds 6 in high yields by reaction with B(C6F5)3 at room temperature. The zwitterionic compounds 6 are conveniently accessible and can be obtained with unique substitution patterns by this route. For two examples, we show the conversion of 6 to the respective 3-borylated phosphole derivatives 7 through multiple 1,1-carboboration reactions. In a useful one-pot methodology, the phosphirenium borates 6 are converted to air-stable 3-arylated phospholes 8 by a sequential 1,1-carboboration/ Suzuki-Miyaura type cross-coupling reaction.