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Picosecond Dynamics of Avobenzone in Solution
Adam D Dunkelberger1, Ryan D Kieda1, Brett M Marsh1
1Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53706, United States.
Avobenzone photoisomerization was studied on the picosecond timescale. Researchers observed two unstable non-chelated enol isomers, providing the first direct evidence and their lifetimes, crucial for sunscreen efficacy.
Area of Science:
- Photochemistry
- Chemical Dynamics
- Spectroscopy
Background:
- Avobenzone, a common sunscreen ingredient, undergoes photoisomerization upon UV exposure.
- This process forms non-chelated enol (NCE) isomers, some of which decrease sunscreen efficacy.
- Previous studies on nanosecond- to microsecond-scales could not characterize unstable NCE isomers.
Purpose of the Study:
- To investigate the picosecond dynamics of avobenzone photoisomerization.
- To directly observe and characterize unstable non-chelated enol isomers.
- To determine the lifetimes and branching ratios of these transient species.
Main Methods:
- Excitation of avobenzone at 350 nm.
- Time-resolved spectroscopy using broadband visible and 266 nm probe pulses.
- Analysis of isomer formation and relaxation dynamics on the picosecond timescale.
Main Results:
- Direct spectroscopic evidence for two unstable NCE isomers of avobenzone.
- Determination of the lifetimes for these newly observed NCE isomers.
- Quantification of the branching ratio between the observed NCE isomer pathways.
Conclusions:
- The picosecond timescale reveals previously unobserved NCE isomers of avobenzone.
- Understanding these unstable isomers is critical for optimizing sunscreen photostability.
- This study provides fundamental insights into avobenzone's photochemical behavior.
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