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11.
Christian Buchgraber Alexander Pogantsch Stefan Kappaun Julia Spanring Wolfgang Kern 《Journal of polymer science. Part A, Polymer chemistry》2006,44(14):4317-4327
Light‐emitting diodes based on organic materials [organic light‐emitting diodes (OLEDs)] have attracted much interest over the past decade. Several different attempts have been made to realize multicolor OLEDs. This article describes a new approach based on energy transfer in a donor/acceptor system. A copolymer containing both donor and acceptor compounds as comonomer units is prepared. The polymer consists of a derivative of a luminescent dye [4‐dicyanmethylene‐2‐methyl‐6‐4H‐pyran (DCM); acceptor compound], which is copolymerized with fluorene (donor compound) to combine the properties of an electroactive polymer with a highly luminescent dye. Photochemical processing is achieved by UV irradiation of this copolymer in the presence of gaseous trialkylsilanes. This reagent selectively saturates the C?C bonds in the DCM comonomer units while leaving the fluorene units essentially unaffected. As a result of the photochemical process, the red electroluminescence of the acceptor compound vanishes, and the blue‐green electroluminescence from the polyfluorene units is recovered. Compared with previous approaches based on polymer blends, this copolymer approach avoids problems associated with phase‐separation phenomena in the active layer of OLEDs. © 2006Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4317–4327, 2006 相似文献
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Abramowicz H Belusevic R Blondel A Blümer H Böckmann P Brummel HD Buchholz P Burkhardt H Debu P Duda J Dydak F Falkenburg B Fiedler M Geiges R Geweniger C Grant AL Guyot C Hagelberg R Hepp V Hughes EW Kampschulte B Keilwerth H Kleinknecht K Knobloch J Krasny M Królikowski J Kurz N Lipniacka A Merlo J Müller E Para A Perez P Perrier F Pollman D Ranjard F Renk B Schuller J Taureg H Tittel K Turlay R Vallage B Wachsmuth H Wotschack J 《Physical review letters》1986,57(3):298-301
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Pérez-Prieto J Galian RE Miranda MA Catalina F Martín-Vargas N López-Ortiz F 《Organic letters》2004,6(4):561-564
[reaction: see text] Several benzo[d]-1,2-oxaphosphole 2-oxides were examined as potential precursors of stabilized C-centered radicals. The transient absorption spectra obtained after laser flash photolysis in the presence of di-tert-butyl peroxide showed the features of benzylic radicals with formation and decay kinetics not significantly influenced by the presence of oxygen. In the case of compounds with two possible diastereomeric forms, the C-H bond of the trans-isomers [corrected] is more reactive toward hydrogen abstraction. 相似文献
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R. Blümel J. Goldberg U. Smilansky 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1988,9(2):95-103
The nearest neighbour level spacing of the quasienergies of a hydrogen atom in a micro-wave field is studied. There is evidence of level repulsion among states corresponding to classically chaotic regions. In the regions of classical phase space where the motion is approximately regular, the corresponding quasienergy spectrum can be understood in terms of approximate dynamical constants. In particular, grouping the high lying quasienergy states into photons yields level spacing plots that are close to δ functions; there is little fluctuation about the average value predicted by the approximate constant. The grouping suggests a simple explanation of the “photon localization” recently observed by Casati et al. [1]. 相似文献