Projects per year
Abstract
Oxybenzone is a common constituent of many commercially available sunscreens providing photoprotection from ultraviolet light incident on the skin. Femtosecond transient electronic and vibrational absorption spectroscopies have been used to investigate the nonradiative relaxation pathways of oxybenzone in cyclohexane and methanol after excitation in the UVA region. The present data suggest that the photoprotective properties of oxybenzone can be understood in terms of an initial ultrafast excited state enol → keto tautomerization, followed by efficient internal conversion and subsequent vibrational relaxation to the ground state (enol) tautomer.
| Original language | English |
|---|---|
| Pages (from-to) | 1363-1368 |
| Number of pages | 6 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 6 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 26 Mar 2015 |
Bibliographical note
Date of Acceptance: 26/03/2015Research Groups and Themes
- Physical & Theoretical
Keywords
- oxybenzone
- sunscreens
- transient absorption spectroscopy
- ultrafast photochemistry
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Dive into the research topics of 'Probing the ultrafast energy dissipation mechanism of the sunscreen oxybenzone after UVA irradiation'. Together they form a unique fingerprint.Projects
- 1 Finished
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Chemical Applications of Velocity & Spatial Imaging
Orr-Ewing, A. J. (Researcher) & Ashfold, M. N. R. (Principal Investigator)
8/01/14 → 31/12/19
Project: Research
Profiles
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Emeritus Professor Michael N R Ashfold
- School of Chemistry - Emeritus Professor
- Soft Matter, Colloids and Materials
Person: Member, Honorary and Visiting Academic
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