2012
DOI: 10.1002/adfm.201200718
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Os(II) Based Green to Red Phosphors: A Great Prospect for Solution‐Processed, Highly Efficient Organic Light‐Emitting Diodes

Abstract: Preparation and characterization of a new class of emissive Os(II) complexes ( 1 -5 ) have been achieved using 3-(thiazol-2-yl), 3-(benzothiazol-2-yl), 3-(imidazol-2-yl) and 3-(benzimidazol-2-yl) azole chelates, together with the incorporation of one diphosphine ancillary for satisfying the octahedral coordination arrangement. The resulting Os(II) complexes, except for 5 , all show bright emission spanning visible region from green to saturated red, and their structural versus spectroscopic properties have bee… Show more

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Cited by 98 publications
(43 citation statements)
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References 67 publications
(29 reference statements)
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“…However, TADF-FlOLED is expected to suffer from unstable efficiencies with driving voltages and temperatures. Thus, phosphorescent OLEDs (PhOLEDs) still dominate high efficiency devices [6][7][8] because of the 100% theoretical IQE [9,10].…”
Section: Introductionmentioning
confidence: 99%
“…However, TADF-FlOLED is expected to suffer from unstable efficiencies with driving voltages and temperatures. Thus, phosphorescent OLEDs (PhOLEDs) still dominate high efficiency devices [6][7][8] because of the 100% theoretical IQE [9,10].…”
Section: Introductionmentioning
confidence: 99%
“…[3] In fluorescent OLEDs, radiative decay of the 75 %t riplet excitons is spin-forbidden and only the 25 %s inglet excitonsl uminesce,w hereas phosphorescent OLEDs can facilitate the singlet-triplet mixingb ye ffective spin-orbit coupling, harvest both singleta nd triplet excitons, thus achieve near-unity internalq uantum efficiency (IQE). [6][7][8][9][10][11][12][13] Neutral complexes of ruthenium(II), [14][15][16] osmium(II), [17][18][19][20] iridium(III), [21][22][23][24][25][26][27] and platinum(II) [4,[28][29][30][31][32][33][34] have been rapidlyd eveloped and widely employed as phosphorescent dopants for polychromic OLEDs. [6][7][8][9][10][11][12][13] Neutral complexes of ruthenium(II), [14][15][16] osmium(II), [17][18][19][20] iridium(III), …”
Section: Introductionmentioning
confidence: 99%
“…As can be seen, all three TFOS sensitizers showed dual MLCT transitions at % 425 and 510 nm, and with molar absorption coefficients greater than 1.1 10 4 mol À1 cm À1 , which were more-orless comparable to the MLCT bands observed in the N719 reference sensitizer. [16] Furthermore, the red-shifting of 3 MLCT absorption for TFOS-2 versus TFOS-1 was clearly attributed to the electron-donating effect of the tert-butyl substituent, which destabilized the HOMO localized at the Os II metal. We attributed this broad peak to the spin-forbidden 3 MLCT absorption, for which the increased absorptivity was clearly the result of enhanced spin-orbit coupling, induced by the heavy-atom effect of the Os II core.…”
Section: Photophysical and Electrochemical Propertiesmentioning
confidence: 97%