Synthesis of regioregular poly(methyl pyridinium vinylene): An isoelectronic analogue to poly(phenylene vinylene)
- 1 February 1995
- journal article
- research article
- Published by Wiley in Advanced Materials
- Vol. 7 (2) , 145-147
- https://doi.org/10.1002/adma.19950070207
Abstract
Poly(phenylene vinylene), PPV, and its derivatives have generated much interest due to their high conductivity and electroluminescent properties which allow for LED applications. Highly electron‐deficient PPV analogues are desirable as they would allow the use of environmentally stable metals as the electrodes in the LEDs. The title compound (see Figure) is just such as material. magnified imageKeywords
This publication has 12 references indexed in Scilit:
- Efficient light-emitting diodes based on polymers with high electron affinitiesNature, 1993
- Self-orienting head-to-tail poly(3-alkylthiophenes): new insights on structure-property relationships in conducting polymersJournal of the American Chemical Society, 1993
- The first regioregular head-to-tail poly(3-hexylthiophene-2,5-diyl) and a regiorandom isopolymer: nickel versus palladium catalysis of 2(5)-bromo-5(2)-(bromozincio)-3-hexylthiophene polymerizationJournal of the American Chemical Society, 1992
- A new synthetic route to polyheteroarenediylvinylenesJournal of the Chemical Society, Chemical Communications, 1991
- Light-emitting diodes based on conjugated polymersNature, 1990
- Poly‐[N,N‐(1,4‐divinylbenzene‐β,β′‐diyl)4,4′‐bipyridinium dibromide], a Novel Conducting Viologen PolymerAngewandte Chemie International Edition in English, 1989
- Poly‐[N,N‐(1,4‐divinylbenzene‐β,β′‐diyl)‐4,4′‐bipyridinium dibromide], a novel conducting viologen polymerAdvanced Materials, 1989
- Benzobisdithiazole (BBDT): an electron spin resonance studyJournal of the American Chemical Society, 1987
- Nucleophilic ethynyl group equivalent and its use in conjugate addition to .alpha.,.beta.-enonesJournal of the American Chemical Society, 1974
- Vinyl Derivatives of the Metals. I. Synthesis of Vinyltin CompoundsJournal of the American Chemical Society, 1957