2002
DOI: 10.1016/s1010-6030(02)00013-8
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Hole-drift mobility in phenylenediamine derivatives possessing methyl substituents

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Cited by 14 publications
(8 citation statements)
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“…The selection of a hole-and electron-conducting core is dictated by the HOMO and LUMO energy levels as well as the charge-carrier mobility. [91][92][93][94][95][96][97][98] The phase transition temperatures included in Chart 1 were determined by differential scanning calorimetry at a heating rate of 20°C/ min.…”
Section: Resultsmentioning
confidence: 99%
“…The selection of a hole-and electron-conducting core is dictated by the HOMO and LUMO energy levels as well as the charge-carrier mobility. [91][92][93][94][95][96][97][98] The phase transition temperatures included in Chart 1 were determined by differential scanning calorimetry at a heating rate of 20°C/ min.…”
Section: Resultsmentioning
confidence: 99%
“…The newly synthesized polymers exhibit high hole drift mobilities and excellent film-forming properties and can be chemically crosslinked in the layer by reaction of the hydroxyl groups with polyisocyanates [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…While it is difficult to draw direct comparisons owing to variations in experimental technique and ultimate molecular composition, some side-byside comparisons are possible (Table 1). Results by Getautis et al 35 are the easiest to compare against the mobility of 2b/PDA where they measured the mobility of a spin-coated sample of unsiliconized 2b/PDA using time-of-flight spectroscopy with near-identical techniques to our current work. At a field strength of 400 (V/cm 2 ) 1/2 , they reported a mobility of 2 × 10 −4 cm 2 /(V s); for 2b/PDA at equivalent field strength and temperature, the mobility is 1 × 10 −4 cm 2 /(V s).…”
Section: ■ Results and Discussionmentioning
confidence: 92%