Issue 29, 2015

Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores

Abstract

Rh-catalysed direct cyclisation of 1,4-naphthoquinones and 9,10-phenanthraquinones with alkynes has been accomplished for the first time through the C–H activation strategy to forge 1,8-dioxapyrenes and 1,12-dioxaperylenes. Starting from readily available substrates, a variety of dipyran-containing PAHs are obtained in one step and exhibit orange/red-emitting performance, large Stokes shifts and high thermal stability.

Graphical abstract: Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores

Supplementary files

Article information

Article type
Communication
Submitted
13 Jan 2015
Accepted
02 Mar 2015
First published
03 Mar 2015

Chem. Commun., 2015,51, 6337-6339

Author version available

Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores

J. Wang, D. Qin, J. Lan, Y. Cheng, S. Zhang, Q. Guo, J. Wu, D. Wu and J. You, Chem. Commun., 2015, 51, 6337 DOI: 10.1039/C5CC00312A

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