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P-Phenylene vinylene

Poly(arylene vinylenes). The use of the soluble precursor route has been successful in the case of poly(arylene vinylenes), both those containing ben2enoid and heteroaromatic species as the aryl groups. The simplest member of this family is poly(p-phenylene vinylene) [26009-24-5] (PPV). High molecular weight PPV is prepared via a soluble precursor route (99—105). The method involves the synthesis of the bis-sulfonium salt from /)-dichloromethylbenzene, followed by a sodium hydroxide elimination polymerization reaction at 0°C to produce an aqueous solution of a polyelectrolyte precursor polymer (11). This polyelectrolyte is then processed into films, foams, and fibers, and converted to PPV thermally (eq. 8). [Pg.38]

Fig. 12. Cyclic voltammograms (corrected with respect to background currents) for the reduction of defined oligo-p-phenylene-vinylenes (THF, NaBPlu)... Fig. 12. Cyclic voltammograms (corrected with respect to background currents) for the reduction of defined oligo-p-phenylene-vinylenes (THF, NaBPlu)...
Janssen FJJ, van Uzendoom LJ, van der Gon AWD, de Voigt MJA, Brongersma HH. 2004. Interface formation between metal and poly-dialkoxy-p-phenylene vinylene. Phys Rev B 70 165425. [Pg.267]

Synthesis of poly(p-phenylene vinylene) films by thermal elimination on a soluble polyelectrolyte. [Pg.445]

Kim SH, Han SK, Park SH, Park LS (1998) A new dithiosquarylium dye for use as an electron transport material in an organic electroluminescent device having poly(p-phenylene vinylene) as an emitter. Dyes Pigm 38 49-56... [Pg.103]

Bushnell and co-workers [117] employed extensive molecular modelling to understand the nature of cis and trans isomerism in tetrahedral p-phenylene vinylene oligomers, and to aid the interpretation of time of flight mass spectrometry and ion mobility studies. Molecules such as T4R, shown in Figure 18, with four equivalent arms can be used to control the crystallinity in thin films. The authors reported the observation of a species in the mass spectrum resulting from the loss of an arm from the central carbon. This species will be referred to as P4R. [Pg.714]

I Sokolik, Z Yang, FE Karasz, and DC Morton, Blue-light electroluminescence from p-phenylene vinylene-based copolymers, J. Appl. Phys., 74 3584—3586, 1993. [Pg.37]

L Smilowitz, A Hays, AJ Heeger, G Wang, and JE Bowers, Time-resolved photoluminescence from poly[2-methoxy, 5-(2-ethyl-hexyloxy)-p-phenylene-vinylene] solutions, gels, films, and blends, J. Chem. Phys., 98 6504-6509, 1993. [Pg.39]

SV Frolov, M Liess, PA Lane, W Gellermann, ZY Yardeny, M Ozaki, and K Yoshino, Exciton dynamics in soluble poly(p-phenylene-vinylene) towards an ultrafast excitonic switch, Phys. Rev. Lett., 78 4285-4288, 1997. [Pg.39]

CC Wu, JKM Chun, PE Burrows, JC Sturm, ME Thompson, SR Forrest, and RA Register, Poly (p-phenylene vinylene)/tris(8-hydroxy) quinoline aluminum heterostructure light emitting diode, Appl. Phys. Lett., 66 653-655, 1995. [Pg.39]

H Antoniadis, MA Abkowitz, and BR Hsieh, Carrier deep-trapping mobility — lifetime products in poly(p-phenylene vinylene), Appl. Phys. Lett., 65 2030-2032, 1994. [Pg.41]

A Kadashchuk, Y Skryshevski, Y Piryatinski, A Vakhnin, EV Emelianova, VI Arkhipov, H Bassler, and J Shinar, Thermally stimulated photoluminescence in poly(2,5-dioctoxy p-phenylene vinylene), J. Appl. Phys., 91 5016-5023, 2002. [Pg.41]

Single- and heterolayer polymeric light emitting diodes based on poly(p-phenylene vinylene) and oxadiazole polymers W. RieB Organic Electroluminescent Materials and Devices, S. Miyata and H.S. Nalwa, Eds., Gordon and Breach, Amsterdam, pp. 73-146... [Pg.48]

Poly(p-Phenylene Vinylene) Homopolymers with Electron-Withdrawing and Donating Substituents... [Pg.69]

Conjugated and Nonconjugated Poly(p-Phenylene Vinylene) Block Copolymers... [Pg.92]

The Best Performing Poly(p-Phenylene Vinylene) Light-Emitting Polymers... [Pg.98]

Preparation of Poly[2-(3,7-dimethyloctyloxy)- 5-methoxy-p-phenylene vinylene] (14) (Chart 2.147). [Pg.247]


See other pages where P-Phenylene vinylene is mentioned: [Pg.237]    [Pg.329]    [Pg.41]    [Pg.180]    [Pg.195]    [Pg.1124]    [Pg.51]    [Pg.52]    [Pg.57]    [Pg.58]    [Pg.62]    [Pg.63]    [Pg.64]    [Pg.245]   
See also in sourсe #XX -- [ Pg.29 ]




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Alkoxy-Substituted Poly(p-Phenylene Vinylenes)

Aryl-Substituted Poly(p-Phenylene Vinylenes)

Conjugated and Nonconjugated Poly(p-Phenylene Vinylene) Block Copolymers

P-phenylene

Poly (p-phenylene vinylenes) (PPVs)

Poly -p-phenylene vinylene

Poly(p-Phenylene Vinylene) Copolymers with Electron Donor and Aryl Substituents

Poly(p-Phenylene Vinylene) Copolymers with Electron-Withdrawing Substituents

Poly(p-Phenylene Vinylene) Homopolymers with Electron-Withdrawing and Donating Substituents

Poly(p-phenylene vinylene) Block Copolymers

Poly(p-phenylene vinylene) Nano Fibers

Poly(phenylene vinylene) (P(PV))

Ring-flip motion of poly(p-phenylene vinylene)

Stretched films of poly(p-phenylene vinylene)

Substituted Poly(p-Phenylene Vinylene) Homopolymers

Synthetic Routes to Poly(p-Phenylene Vinylenes)

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