Excited-state photophysics of an acridine derivative selectively intercalated in duplex DNA

Stephan Hess, William B. Davis, Alexander A. Voityuk, Notker Rösch, Maria E. Michel-Beyerle, Nikolaus P. Ernsting, Sergeij A. Kovalenko, J. Luis Pérez Lustres

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Faster than 200 fs is the time scale of dynamic solvation of an acridine derivative (ACMA) intercalated into an abasic site of the DNA duplex. This observation implies that the Strokes shift of).41 eV is due to ultrafast repolarization od the nuclear degrees of freedom of the DNA pocket. in this system, the environmental reorganization induced by the dipole moment change of 3-4 Debye upon excitation may involve both π-π interactions between ACMA and the adjacent nucleobases as well as polar interactions exerted by the hydrogen bonds of these base pairs.

Original languageEnglish
Pages (from-to)452-455
Number of pages4
JournalChemPhysChem
Volume3
Issue number5
DOIs
StatePublished - 17 May 2002

Keywords

  • DNA
  • Flourescent probes
  • Intercalations
  • Semiempirical Calculations
  • Time-resolved spectroscopy

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