Spectroscopy and Photophysics of Monomethyl-Substituted Derivatives of 5-Deazaalloxazine and 10-Ethyl-5-Deaza-Isoalloxazine

J Fluoresc. 2014 Mar;24(2):505-21. doi: 10.1007/s10895-013-1320-9. Epub 2013 Nov 23.

Abstract

Steady-state and time-resolved spectra were used to describe the singlet and triplet states of 8-methyl-5-deazaalloxazine (8-Me-5-DAll), 9-methyl-5-deazaalloxazine (9-Me-5-DAll) and 10-ethyl-5-deaza-isoalloxazine (10-Et-5-DIAll). Solvatochromic properties were described using different polarity scales, including Δf and the four-parameter scale proposed by Catalán. The results indicate that the Catalán scale shows a strong influence of solvent acidity (hydrogen-bond donating ability) on the emission properties of 8-Me-5-DAll and 9-Me-5-DAll. These results indicate the importance of intermolecular solute-solvent hydrogen-bonding interactions in the excited state of these compounds. Contrary to deazaalloxazines, solvent acidity affects the absorption spectra of 10-Et-5-DIAll. Fluorescence lifetimes and quantum yields and also transient absorption spectra were determined for all of the compounds studied. Electronic structure and S(0)-S(i), S(0)-T(i ), T(1)-T(i) transitions energies and oscillator strengths were calculated using the TD-DFT methods. Theoretical calculations were compared to experimental data.

Keywords: 5-deaza-isoalloxazine; 5-deazaalloxazine; Photophysics; Spectroscopy; TD-DFT study; Transient absorption spectra.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Oxazines / chemistry*
  • Proton Magnetic Resonance Spectroscopy
  • Spectrometry, Fluorescence / methods*
  • Spectrophotometry, Ultraviolet

Substances

  • Oxazines