1997
DOI: 10.1016/s0022-2313(96)00396-1
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Starburst molecules based on π-electron systems as materials for organic electroluminescent devices

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Cited by 90 publications
(56 citation statements)
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“…The HOMO± LUMO energy gaps of TPhB, TBPhB, TTPhB, and TTPhPhB were estimated to be approximately 3.5 eV from the energy thresholds of their electronic absorption spectra. Based on the reduction potential (±2.01 V vs. Ag/Ag + ) and the LUMO energy level (3.1 eV) of Alq 3 , [13] the LUMO energy levels of TPhB, TBPhB, TTPhB, and TTPhPhB were estimated to be ca. 2.6 eV from the values of their half-wave reduction potentials.…”
Section: Molecular Properties Of Tphb Tbphb Ttphb and Ttphphbmentioning
confidence: 99%
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“…The HOMO± LUMO energy gaps of TPhB, TBPhB, TTPhB, and TTPhPhB were estimated to be approximately 3.5 eV from the energy thresholds of their electronic absorption spectra. Based on the reduction potential (±2.01 V vs. Ag/Ag + ) and the LUMO energy level (3.1 eV) of Alq 3 , [13] the LUMO energy levels of TPhB, TBPhB, TTPhB, and TTPhPhB were estimated to be ca. 2.6 eV from the values of their half-wave reduction potentials.…”
Section: Molecular Properties Of Tphb Tbphb Ttphb and Ttphphbmentioning
confidence: 99%
“…[8,16,17] They have been used as good hole transporters in Alq 3 -based green-emitting organic EL devices. [2,9,13,18] As described in the introduction, the use of these materials as blue-or blue±violet emitters instead of hole transporters in organic EL devices requires the presence of either an electron transporter with an effective hole-blocking ability, or a hole blocker inserted in between the emitting layer and the electron-transport layer. A device using TPD as an emitter and 3-(biphenyl-4-yl)-4-phenyl-5-(4-tert-butylphenyl)-1,2,4-triazole (TAZ) as an electron transporter has been reported; however, the emission from TPD is accompanied by another stronger emission, peaking at 460 nm, [16] which may be attributable to the emission from an exciplex formed between TPD and TAZ.…”
Section: Fabrication and Performance Of Blue-and Blue±violet-emittingmentioning
confidence: 99%
“…Many different structures of electron donor fragments are introduced (compounds 45-57 in Fig.13) in the pyranylidene backbone after introducing the electron acceptor fragment [1,[4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][27][28][29]31]. In cases where only one methyl group reacts with the aldehyde, a mono-styryl derivative of pyranylidene is obtained (see Fig.13).…”
Section: Synthesis Of Pyranilydene and Isophorene Type Red Luminescenmentioning
confidence: 99%
“…We have previously shown that multilayer organic EL devices consisting of the emitting layer of Alga and double hole-transport layers of m-MTDATA as HTL 1 and TPD or other holetransporting materials as HTL2 (Figure 1), exhibits higher luminous efficiency and significantly enhanced operational durability than the corresponding double layer device in the absence of m-MTDATA [3,12]. In the present study, materials with higher glass-transition temperatures (Tgs), [13] are used as HTL 1 and HTL 2, respectively, in order to investigate annealing effect on charge injection in organic EL devices.…”
Section: Introductionmentioning
confidence: 99%