Issue 2, 2013

Excited states of menthyl anthranilate: a UV-A absorber

Abstract

The photophysical properties of menthyl anthranilate (MA), a UV-A absorber, have been studied through measurements of UV absorption, fluorescence, triplet–triplet absorption and time-resolved thermal lens in ethanol at room temperature and/or 77 K. The phosphorescence and time-resolved electron paramagnetic resonance spectra have also been observed in ethanol at 77 K. The energy levels of the lowest excited singlet (S1) state and triplet (T1) state were determined. The quantum yields of fluorescence, phosphorescence and S1 → T1 intersystem crossing (ISC) were also determined. From the data on the lifetime and quantum yield, the rate constants of the radiative decay, internal conversion and ISC of the excited states of MA were determined. The exceptionally high ISC quantum yield of MA shows that the deactivation processes of the S1 state of MA are different from those of most UV absorbers such as cinnamate, salicylate, 2-hydroxybenzophenone, benzotriazole and dibenzoylmethane derivatives, where the internal conversion rates of the S1 states are much faster than the ISC rates. The observed T1 lifetime and zero-field splitting parameters suggest that the T1 state of MA possesses almost pure 3ππ* character.

Graphical abstract: Excited states of menthyl anthranilate: a UV-A absorber

Article information

Article type
Paper
Submitted
15 Jun 2012
Accepted
20 Aug 2012
First published
21 Aug 2012

Photochem. Photobiol. Sci., 2013,12, 246-253

Excited states of menthyl anthranilate: a UV-A absorber

A. Kikuchi, K. Shibata, R. Kumasaka and M. Yagi, Photochem. Photobiol. Sci., 2013, 12, 246 DOI: 10.1039/C2PP25190F

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.

Spotlight

Advertisements