Issue 1, 2010

A novel substitution reaction of perylene bisimides with Ph2PLi at the α-position

Abstract

A novel substitution reaction of perylene bisimides has been developed. The Ph2PO group was attached to the PBI core at the α-position instead of the usual bay position. This substitution kept the high fluorescence of the PBI dyes and caused the adjacent proton at the bay position and a tertiary proton at the cyclohexyl group to be shifted significantly in the 1H-NMR spectra.

Graphical abstract: A novel substitution reaction of perylene bisimides with Ph2PLi at the α-position

Supplementary files

Article information

Article type
Paper
Submitted
01 Jun 2009
Accepted
27 Jul 2009
First published
23 Oct 2009

New J. Chem., 2010,34, 61-64

A novel substitution reaction of perylene bisimides with Ph2PLi at the α-position

X. Wu, C. Yin, Z. Shi, M. Xu, J. Zhang and J. Sun, New J. Chem., 2010, 34, 61 DOI: 10.1039/B9NJ00364A

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