2002
DOI: 10.1002/1521-4095(20020805)14:15<1061::aid-adma1061>3.0.co;2-6
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Polyfluorenes with Dendron Side Chains as the Active Materials for Polymer Light-Emitting Devices

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Cited by 199 publications
(137 citation statements)
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“…It should be noted that a comparable level of delayed aggregate emission in the two materials is compatible with the observation that the charge-transporting properties of PF are not dramatically modified upon dendronization. [3,25] As chain-to-chain transport is expected to be most efficient at sites of aggregation, which exist in both materials, it is not surprising that the insulating dendrons do not result in the bulk film becoming more insulating. By contrast, a strong dependence of charge transport on dendronization has been observed in a family of macromolecular dendrimers.…”
Section: Resultsmentioning
confidence: 99%
“…It should be noted that a comparable level of delayed aggregate emission in the two materials is compatible with the observation that the charge-transporting properties of PF are not dramatically modified upon dendronization. [3,25] As chain-to-chain transport is expected to be most efficient at sites of aggregation, which exist in both materials, it is not surprising that the insulating dendrons do not result in the bulk film becoming more insulating. By contrast, a strong dependence of charge transport on dendronization has been observed in a family of macromolecular dendrimers.…”
Section: Resultsmentioning
confidence: 99%
“…It has been demonstrated that adding dendritic bulky moieties can effectively suppress the formation of aggregation (Ego et al, 2002;Marsitzky et al, 2001) and reduce self-quenching of luminescence duo to intermolecular interactions. (Pogantsch et al, 2002) In addition, a good film-forming ability, a good morphological stability and a high thermal stability also are crucial to the practical application of PLED. (Smith et al, 1998;Fenter et al, 1997) They can be improved by increasing the molecular weight of the EL polymer materials or introducing, compounding the thermostable groups or molecules into the EL polymer materials.…”
Section: Introductionmentioning
confidence: 99%
“…This unique molecular architecture therefore allows independent optimization of the optoelectronic and processing properties. [5][6][7] Since the first report on the use of triplet emitters in OLEDs by Forrest and Thompson, [8] electrophosphorescent devices have attracted a great deal of interest, in which metal-organic complexes of Ru(II), Os(II), or Ir(III) are doped into charge transporting host materials as the emitting centers.…”
Section: Introductionmentioning
confidence: 99%