Issue 43, 2014

Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines

Abstract

An unexpected discovery of the novel cyclocondensation reaction of 1,8-diazabicyclo[5.4.0]undec-8-ene (DBU) and 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) with alkyl coumarin-3-carboxylates is described. First, an unknown skeleton is generated through the concomitant formation of new nitrogen–carbon and carbon–carbon bonds followed by the oxidation of the intermediate product by the second equivalent of the starting coumarin. Pentacyclic DBN-derivatives exhibit strong fluorescence both in solutions (Φfl ∼ 0.6–0.8) and in the solid state, while non-planar DBU-derivatives exhibit strong fluorescence in the solid state only.

Graphical abstract: Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines

Supplementary files

Article information

Article type
Communication
Submitted
11 Feb 2014
Accepted
05 Mar 2014
First published
07 Mar 2014

Chem. Commun., 2014,50, 5688-5690

Author version available

Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines

Y. M. Poronik and D. T. Gryko, Chem. Commun., 2014, 50, 5688 DOI: 10.1039/C4CC01106F

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