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On 3,5,6-trihalo-2-(pyrrol-2-yl)-1,4-benzoquinones

✍ Scribed by Ribó, Josep M. ;Acero, Carles


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
674 KB
Volume
1995
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

In the reaction of pyrroles with tetrahalo‐1,4‐benzoquinones two different processes occur: the oxidation of pyrrole and the coupling reaction to 3,5,6‐trihalo‐2‐(pyrrol‐2‐yl)‐1,4‐benzoquinones. Excess of pyrrole results in doped polypyrrole as the principal reaction product. Excess of tetrahalobenzoquinone and dilution, provides the title compounds. The UV/Vis spectra and the electrochemical behaviour show that the title compounds have the HOMO localized at the pyrrole and the LUMO at the quinone ring.


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