Asymmetrically twisted phenanthrimidazole derivatives as host materials for blue fluorescent, green and red phosphorescent OLEDs

The electroluminescent properties of asymmetrically twisted phenanthrimidazole derivatives comprised of fluorescent anthracene or pyrene unit namely, 1-(1-(anthracen-10-yl)naphthalen-4-yl)-2-styryl-1H-phenanthro[9,10-d]imidazole (ANSPI), 1-(1-(pyren-1-yl) naphthalene-4-yl)-2-styryl-1H-phenanthro[9,10-d]imidazole (PNSPI), 4-(2-(4-(anthracen-9-yl) styryl)-1H-phenanthro[9,10-d]imidazol-1-yl)naphthalene-1-carbonitrile (ASPINC) and 4-(2-(4-(pyren-1-yl)styryl)-1H-phenanthro[9,10-d]imidazol-1-yl)naphthalene-1-carbonitrile (PSPINC) for blue OLEDs have been analyzed. The asymmetrically twisted conformation interrupt p-conjugation effectively results in deep-blue emission. The pyrene containing PSPINC based non-doped blue device (476nm) shows maximium efficiencies (current efficiency (eta(c))-4.23cd/A; power efficiency (eta(p))-2.86lm/W; external quantum efficiency (eta(ex))-3.48%: CIE (0.16, 0.17) at 3.10V. Among the doped blue devices, An(PPI)2:ASPINC shows high efficiencies (eta(c)-12.13cd/A; eta(p)-5.98lm/W; eta(ex)-6.79%; L-23986 cd m(-2); EL-458 nm) at 3.15V with CIE (0.15, 0.17) than An(PPI)2:PSPINC based device which is inconsistent with non-doped device performances. The green and red PhOLEDs show higher efficiencies with Ir(ppy)3: ASPINC (eta(c)-50.6cd/A; eta(p)-53.4lm/W; eta(ex)-17.0%; L-61581 cd m(-2); EL-501 nm, CIE (0.31, 0.60) at 3.32V and (bt)2Ir(dipba): ASPINC (eta(c)-15.2cd/A; eta(p)-16.5lm/W; eta(ex)-14.5%; L-13456 cd m(-2); EL-610 nm), CIE (0.63, 0.36) at 3.20V, respectively. The complete energy transfer between the host and dopant molecules improved the efficiency of PHOLEDs.