Issue 18, 2011

Luminescent bichromophoric spiroindolones – synthesis and electronic properties

Abstract

Novel bichromophoric spirocyclic indolones have been synthesized by an insertion–coupling–isomerization–Diels–Alder domino reaction. The emission colors are strongly affected by the substituents: N-Boc leads to intense blue fluorescence, N-dansyl causes turquoise emission, whereas a 1-anthryl substituent on the butadiene results in yellow luminescence. The latter behavior is rationalized by TDDFT computations as a result of significant geometrical changes.

Graphical abstract: Luminescent bichromophoric spiroindolones – synthesis and electronic properties

Supplementary files

Article information

Article type
Communication
Submitted
03 May 2011
Accepted
01 Jul 2011
First published
04 Jul 2011

Org. Biomol. Chem., 2011,9, 6196-6199

Luminescent bichromophoric spiroindolones – synthesis and electronic properties

J. Schönhaber and T. J. J. Müller, Org. Biomol. Chem., 2011, 9, 6196 DOI: 10.1039/C1OB05703K

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