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Kumada polythiophenes

The Synthesis of Conjugated Polythiophenes by Kumada Cross-Coupling... [Pg.155]

The Kumada cross-coupling was first utilized in 1980 to prepare unsubstituted polythiophene, via the nickel-catalyzed cross-coupling of 2-bromo-5-mag-nesiobromothiophene, produced by inserting magnesium metal into 2,5-dibromothiophene [27, 28]. The poor solubility of the polymer resulted... [Pg.158]

I 7 The Synthesis of Conjugated Polythiophenes by Kumada Cross-Coupling Table 7.2 Polymerization data for symmetrical and fused thiophenes. [Pg.182]

Migita-Kosugi-Stille, Negishi-Baba, Mizoroki-Heck, and Kumada-Tamao-Corriu coupling) and for polythiophene synthesis. Direct arylation (see Chapter 4) was highlighted as one of the more efficacious methods. [Pg.14]

One of the most highly researched conjugated polymers is poly(3-aIkylthiophene) (underivatized polythiophene is insoluble). In a synthetic method developed by McCullough [94, 96] and further modified by Yokozawa [95, 97], Kumada catalyst-transfer polycondensation (KCTP), also commonly known as Grignard metathesis polymerization... [Pg.23]

Early preparations of polythiophene employed both electrochemical and chemical methods [1,21-23]. Chemical preparations via oxidative coupling of thiophene or Kumada cross-coupling of Grignard reagents... [Pg.225]


See other pages where Kumada polythiophenes is mentioned: [Pg.139]    [Pg.230]    [Pg.600]    [Pg.43]    [Pg.158]    [Pg.159]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.167]    [Pg.169]    [Pg.171]    [Pg.173]    [Pg.173]    [Pg.177]    [Pg.179]    [Pg.181]    [Pg.183]    [Pg.185]    [Pg.187]    [Pg.662]    [Pg.1199]    [Pg.209]   
See also in sourсe #XX -- [ Pg.158 , Pg.159 , Pg.160 , Pg.161 , Pg.162 , Pg.163 , Pg.164 ]




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