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Thienothiophenes copolymers

Thienothiophene Copolymers in Field Effect Transistors 657 Table 17.1 Properties of thienothiophene-containing polymers... [Pg.657]

M. C. Gather, M. Heeney, W. Zhang, K. S. Whitehead, D. C. C. Bradley, I. McCulloch and A. J. Campbell, An afignable fiuorene thienothiophene copolymer with deep-blue electroluminescent emission at 410 nm. Chem. Commun., 1079-1081 (2008). [Pg.670]

The highest mobilities achieved in solution-deposited polymer transistor devices have been exhibited by thiophene-containing polymers. Thiophene is an electron-rich, planar aromatic heterocycle, which can form a range of conjugated polymers when coupled appropriately [23, 24], The crystalline nature of many thiophene derivatives plays a role in their excellent charge transport properties. In this chapter, we will focus on copolymers of thiophene with the fused unit, thienothiophene, and their structural analogues. [Pg.651]

An excellent demonstration of the benefits of the self-assembly properties of liquid crystalline phases lies in the recent development of liquid crystalline, semiconducting, thiophene polymers and copolymers, many of which contain thienothiophene groups [11-17], see polymer 2, poly(2,5-bis(3-alkylthiophen-2-yl)thieno [3,2-b]thiophene) (pBTTT), for example, which exhibits exceptionally... [Pg.251]


See other pages where Thienothiophenes copolymers is mentioned: [Pg.152]    [Pg.647]    [Pg.651]    [Pg.653]    [Pg.655]    [Pg.659]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.667]    [Pg.667]    [Pg.669]    [Pg.671]    [Pg.435]    [Pg.244]    [Pg.266]    [Pg.152]    [Pg.647]    [Pg.651]    [Pg.653]    [Pg.655]    [Pg.659]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.667]    [Pg.667]    [Pg.669]    [Pg.671]    [Pg.435]    [Pg.244]    [Pg.266]    [Pg.777]    [Pg.656]    [Pg.656]    [Pg.336]    [Pg.128]    [Pg.114]   
See also in sourсe #XX -- [ Pg.667 ]




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Thienothiophene

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