Issue 20, 2001

Polyaromatic amines. Part 2. Synthesis of 4,4′,4″-tris(N-aryl-N-phenylamino)triphenylamine, N,N-bis[4-(N-aryl-N-phenylamino)phenyl]tolylamine and N,N,N′,N′-tetraaryl-o-phenylenediamine derivatives

Abstract

The title compounds were synthesised and characterised as part of a study into new aromatic amines for charge transporting materials. Proton and carbon spectral data for compounds 1–6 were obtained in C6D6 as a consequence of their facile oxidation in CDCl3. Each compound was characterised by cyclic voltammetry. An estimate of the intramolecular charge mobility was deduced from the difference between the first and second oxidation potentials.

Graphical abstract: Polyaromatic amines. Part 2. Synthesis of 4,4′,4″-tris(N-aryl-N-phenylamino)triphenylamine, N,N-bis[4-(N-aryl-N-phenylamino)phenyl]tolylamine and N,N,N′,N′-tetraaryl-o-phenylenediamine derivatives

Article information

Article type
Paper
Submitted
12 Jul 2001
Accepted
11 Sep 2001
First published
01 Oct 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 2548-2552

Polyaromatic amines. Part 2. Synthesis of 4,4′,4″-tris(N-aryl-N-phenylamino)triphenylamine, N,N-bis[4-(N-aryl-N-phenylamino)phenyl]tolylamine and N,N,N′,N′-tetraaryl-o-phenylenediamine derivatives

M. J. Plater and T. Jackson, J. Chem. Soc., Perkin Trans. 1, 2001, 2548 DOI: 10.1039/B106273P

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements