Journal of Physical Chemistry p. 17079 - 17082 (1996)
Update date:2022-08-16
Topics:
Bonvoisin, Jacques
Launay, Jean-Pierre
Verbouwe, Wouter
Auweraer, Mark Van der
Schryver, Frans Carl De
This paper is devoted to two new aromatic polyamines derived from p-EFTP (5'-(4-(bis(4-ethylphenyl)amino)phenyl-N,N,N',N'-tetrakis(4-ethylphenyl)-1,1':3',1"-terphenyl-4,4"-diamine) and exhibiting meta connections around a central phenylene ring.In p-EFDP (5'-phenyl-(N,N,N',N'-tetrakis(4-ethylphenyl)-1,1':3',1"-terphenyl-4,4"-diamine) there are only two redox sites instead of three.Upon partial oxidation, an intervalence transition is observed from which an electronic coupling very similar to the one of p-EFTP is obtained.In p-FADP (N,N,N',N',N",N"-hexakis(4-ethylphenyl)- 1,1':3',1"-terphenyl-4,4",5'-triamine) one finds two redox sites of the N,N'-bis(4-ethylphenyl)-4-aminobiphenyl type, and one redox site of the triphenylamine type.The analysis of the electrochemical behavior and of the intervalence transitions in the mono- and dioxidized species allows the distinction among the different types of electron transfer.
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