Issue 27, 2011

Binaphthyl platform as starting materials for the preparation of electron rich benzo[g,h,i]perylenes. Application to molecular architectures based on amino benzo[g,h,i]perylenes and carborane combinations

Abstract

Valuable amino benzo[g,h,i]perylenes have been obtained through a one pot electrophilic aromatic substitution—Scholl reaction sequence. Novel molecular architectures combining 3D-o-carborane and planar amino benzo[g,h,i]perylene units are described. Photophysical properties of amino benzo[g,h,i]perylene and the carborane-appended derivatives are discussed.

Graphical abstract: Binaphthyl platform as starting materials for the preparation of electron rich benzo[g,h,i]perylenes. Application to molecular architectures based on amino benzo[g,h,i]perylenes and carborane combinations

Supplementary files

Article information

Article type
Communication
Submitted
12 Apr 2011
Accepted
17 May 2011
First published
07 Jun 2011

Chem. Commun., 2011,47, 7725-7727

Binaphthyl platform as starting materials for the preparation of electron rich benzo[g,h,i]perylenes. Application to molecular architectures based on amino benzo[g,h,i]perylenes and carborane combinations

G. Pieters, A. Gaucher, D. Prim, T. Besson, J. Giner Planas, F. Teixidor, C. Viñas, M. E. Light and M. B. Hursthouse, Chem. Commun., 2011, 47, 7725 DOI: 10.1039/C1CC12099A

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