Effect of Isomerization on Excited-State Dynamics of Carotenoid Fucoxanthin

Ultrafast transient absorption spectroscopy and single-wavelength anisotropy measurements were used to study the effect of isomerization on the excited-state properties of fucoxanthin in polar and nonpolar solvents. The excitation wavelengths were 477 nm for all-<i>trans</i>-fucoxanthin, and 333 and 477 nm for <i>cis</i>-fucoxanthin. All transient absorption spectra of the fucoxanthin isomers in polar solvents show intramolecular charge transfer (ICT) state features, typical for carbonyl carotenoids. Global analysis of the data requires an additional fitting component, originated from the presence of blue and red forms of fucoxanthin in a polar protic solvent. Here we demonstrate that the ICT state decays faster than the S₁ state, due to the significant contribution of the red form to the ICT state dynamics. The isomerization does not affect the S₁ lifetime, but induces a larger difference between the S₁- and ICT-state lifetimes in <i>cis</i>-fucoxanthin, which is likely caused by alterations of ICT coupling to either the S₁ or S₀ states; the S*-state signal is more pronounced for <i>cis</i>-isomers in a nonpolar solvent