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Synthesis of π-Conjugated 2,2:6′,2″-Terpyridine-Substituted Oligomers Based on 3,4-Ethylenedioxythiophene

✍ Scribed by Fillaud, Laure; Trippé-Allard, Gaëlle; Lacroix, Jean Christophe

Book ID
119966279
Publisher
American Chemical Society
Year
2013
Tongue
English
Weight
413 KB
Volume
15
Category
Article
ISSN
1523-7060

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ChemInform Abstract: Novel Synthesis of
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✍ R.-A. FALLAHPOUR; E. C. CONSTABLE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Novel Synthesis of Substituted 4'-Hydroxy-2,2':6',2"-terpyridines. -The Kroehnke-methodology is applied to diacetylpyridine (II). Thus the terpyridines (V), (VII), and (IX) are synthesized with substituents at C-4, C-5 and C-6 of both terminal pyridines while the 4'-position is functionalized as a