4.6 Article

Luminescent bichromophoric spiroindolones - synthesis and electronic properties

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 18, Pages 6196-6199

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob05703k

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG)
  2. Fonds der Chemischen Industrie

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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.

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