Ultrafast non-adiabatic dynamics of stilbene-based plant-derived sunscreens with cis-trans isomerization structures.
Spectrochim Acta A Mol Biomol Spectrosc
; 298: 122759, 2023 Oct 05.
Article
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| MEDLINE
| ID: mdl-37119635
ABSTRACT
In this work, we investigated the potential UV protection mechanism of the natural compounds hydroxy resveratrol and pterostilbene by combining theoretical calculations and femtosecond transient absorption spectra (FTAS). The UV absorption spectra showed that the two compounds exhibited strong absorption properties and high photostability. We found two molecules will reach the S1 state or an even higher excited state after UV exposure and molecules in S1 will cross a lower energy barrier to reach the conical intersection. The adiabatic trans-cis isomerization process happened and finally return to the ground. Meanwhile, FTAS clarified the time scale of trans-cis isomerization of two molecules was â¼ 10 ps, which also met the requirement of fast energy relaxation. This work also provides theoretical guidance for developing new sunscreen molecules from natural stilbene.
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MEDLINE
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En
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Spectrochim Acta A Mol Biomol Spectrosc
Asunto de la revista:
BIOLOGIA MOLECULAR
Año:
2023
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Article