Time-resolved spectroscopy of the singlet excited state of betanin in aqueous and alcoholic solutions

Phys Chem Chem Phys. 2015 Jul 21;17(27):18152-8. doi: 10.1039/c5cp00684h.

Abstract

The photophysical properties of betanin in aqueous and alcoholic solutions were determined at room temperature using ultrafast UV-vis-NIR transient absorption spectroscopy (λexc = 535 nm). Its S1 → Sn (n > 1) absorption bands appear with maxima at about λ ∼ 450 and 1220 nm. The short betanin S1 state lifetime (6.4 ps in water) is mainly determined by the efficient S1 → S0 radiationless relaxation, probably requiring a strong change in geometry, since the S1 lifetime grows to 27 ps in the more viscous ethylene glycol. The fluorescence quantum yield is very low (Φf ∼ 0.0007 in water), therefore this deactivation path is of minor importance. Other processes, such as S1 → T1 intersystem crossing or photoproduct formation, are virtually absent, since full S0 ← S1 ground state recovery is observed within tens of picoseconds after photoexcitation. The observed fast light-to-heat conversion in the absence of triplet excited state formation supports the idea that betanin is a photoprotector in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Betacyanins / chemistry*
  • Ethylene Glycol / chemistry
  • Methanol / chemistry*
  • Quantum Theory
  • Solutions / chemistry
  • Spectrometry, Fluorescence
  • Water / chemistry*

Substances

  • Betacyanins
  • Solutions
  • Water
  • betanin
  • Ethylene Glycol
  • Methanol