Issue 12, 2009

The synthesis of novel core-substituted naphthalene diimides via Suzuki cross-coupling and their properties

Abstract

This paper reports the efficient core-substitution of halogenated naphthalene diimides utilizing the Suzuki cross-coupling reaction to install various aryl substituents at the 2,6 positions. The UV-visible spectra of these compounds show a clear absorbance red shift and an enhanced fluorescence output, making them potential candidates for solar-cell dyes and electroactive elements for supramolecular materials.

Graphical abstract: The synthesis of novel core-substituted naphthalene diimides via Suzuki cross-coupling and their properties

Supplementary files

Article information

Article type
Letter
Submitted
18 Jul 2009
Accepted
02 Oct 2009
First published
28 Oct 2009

New J. Chem., 2009,33, 2409-2413

The synthesis of novel core-substituted naphthalene diimides via Suzuki cross-coupling and their properties

S. V. Bhosale, M. B. Kalyankar, S. V. Bhosale, S. J. Langford, E. F. Reid and C. F. Hogan, New J. Chem., 2009, 33, 2409 DOI: 10.1039/B9NJ00476A

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