Issue 30, 2009

Facile method for spectroscopic examination of radical ions of hydrophilic carotenoids

Abstract

Hydrophilic carotenoids, unusual members of an intrinsically hydrophobic family, and their radical ions are important reactants. An all-optical method for generating singly charged radical ions of a hydrophilic carotenoid (Car) is described. It relies on photolyzing an aqueous mixture of Car and a photoionizable auxiliary solute (A), and making conditions conducive to the capture, by Car, of the hydrated electron (eaq) or the positive hole in A˙+ or both. When A is Trolox (TOH), only eaq can be captured, since TOH˙+ deprotonates too rapidly to be a hole donor; when A is Trolox methyl ether (TOMe), both Car˙ and Car˙+ are formed, since TOMe˙+ lives long enough to transfer its positive hole to Car; formation of Car˙ is prevented under aerobic conditions.

Graphical abstract: Facile method for spectroscopic examination of radical ions of hydrophilic carotenoids

Article information

Article type
Paper
Submitted
18 Mar 2009
Accepted
07 May 2009
First published
09 Jun 2009

Phys. Chem. Chem. Phys., 2009,11, 6401-6405

Facile method for spectroscopic examination of radical ions of hydrophilic carotenoids

K. R. Naqvi, T. B. Melø, T. Jávorfi, S. González-Pérez and J. B. Arellano, Phys. Chem. Chem. Phys., 2009, 11, 6401 DOI: 10.1039/B905454E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements