1998
DOI: 10.1117/12.332598
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<title>Vinylene-bridged triphenylamine dimers as an emitting material in trilayer organic electroluminescent devices</title>

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Cited by 9 publications
(2 citation statements)
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“…On the contrary, the electron-withdrawing p -cyanophenyl moiety in 13 significantly shifts the first oxidation potential anodically. Stabilization of the cation radicals by electron-donating substituents at a distant conjugation is well documented, particularly when the moieties involved are in communication. 6b, …”
Section: Resultsmentioning
confidence: 94%
“…On the contrary, the electron-withdrawing p -cyanophenyl moiety in 13 significantly shifts the first oxidation potential anodically. Stabilization of the cation radicals by electron-donating substituents at a distant conjugation is well documented, particularly when the moieties involved are in communication. 6b, …”
Section: Resultsmentioning
confidence: 94%
“…Many of these systems have shown amplified spontaneous emission (ASE) thresholds much lower than those of traditional dyes, mostly due to the possibility of increasing the amount of materials in the films without significant PL quenching. N,N 0 -diphenyl-N,N 0 -bis(3-methylphenyl)-(1,1 0 -biphenyl)-4,4 0 -diamine (TPD) receives significant attention serve as solid state laser material over the years due to the broad photoluminescence and the tunable wide laser wavelength range [1][2][3][4] on account of its optical properties, absorption and emission behavior [5,6]. TPD shows stimulated emission in neat films that were fabricated by spin-coating, vacuum thermal evaporation and ink-jet printing as well as the blends that is diluted in polystyrene (PS) [7][8][9][10].…”
Section: Introductionmentioning
confidence: 99%