Decoding the excited-state dynamics of carbonyl-containing carotenoids: Insights from the Ind series

Biochim Biophys Acta Mol Cell Biol Lipids. 2025 Apr;1870(3):159598. doi: 10.1016/j.bbalip.2025.159598. Epub 2025 Jan 28.

Abstract

Carotenoids are naturally occurring pigments essential for both light-harvesting and photoprotection in photosynthetic processes. Among these, carbonyl-containing carotenoids exhibit distinctive excited state properties due to the presence of intramolecular charge transfer (ICT) in their excited states. In this study, we synthesized a novel family of carotenoid analogs with varying numbers of conjugated double bonds, denoted as the Ind series, and conducted femtosecond pump-probe spectroscopy on these molecules in both acetone and n-hexane. The objective was to elucidate how the excited-state dynamics depend on the conjugation length. The spectroscopic characterization of the Ind series revealed several unique features: the observation of stimulated emission from the 1Ag-/ICT state, the emergence of the 1 state, triplet state formation mediated by the 1 state, and an anomalous solvent dependence of the 1Ag-/ICT state lifetimes. The relationship between conjugation length and excited state dynamics, as well as the ICT character of the Ind series, are thoroughly discussed.

Keywords: Carotenoids; Excited state dynamics; Intramolecular charge transfer; Ultrafast spectroscopy.

MeSH terms

  • Acetone / chemistry
  • Carotenoids* / chemistry
  • Hexanes / chemistry

Substances

  • Carotenoids
  • Acetone
  • Hexanes
  • n-hexane