Structural characterization of astaxanthin aggregates as revealed by analysis and simulation of optical spectra

Abstract

Carotenoids can self–assemble in hydrated polar solvents to form J– or H–type aggregates, inducing dramatic changes in photophysical properties. Here, we measured absorption and emission spectra of astaxanthin in ethanol–water solution using ultraviolet–visible and fluorescence spectrometers. Two types of aggregates were distinguished in mixed solution at different water contents by absorption spectra. After addition of water, all probed samples immediately formed H–aggregates with maximum blue shift of 31nm. In addition, J–aggregate was formed in 1:3 ethanol–water solution measured after an hour. Based on Frenkel exciton model, we calculated linear absorption and emission spectra of these aggregates to describe aggregate structures in solution. For astaxanthin, experimental results agreed well with the fitted spectra of H–aggregate models, which consisted of tightly packed stacks of individual molecules, including hexamers, trimers, and dimers. Transition moment of single astaxanthin in ethanol was obtained by Gaussian 09 program package to estimate the distance between molecules in aggregates. Intermolecular distance of astaxanthin aggregates ranges from 0.45nm to 0.9nm. Fluorescence analysis showed that between subbands, strong exciton coupling induced rapid relaxation of H–aggregates. This coupling generated larger Stokes shift than monomers and J–aggregates.