超快激光光谱学
激发态
吸收(声学)
吸收光谱法
顺反异构
吸收带
光化学
谱线
光谱学
化学
分析化学(期刊)
类胡萝卜素
材料科学
叶黄素
原子物理学
立体化学
有机化学
光学
物理
天文
复合材料
食品科学
量子力学
作者
Dariusz M. Niedzwiedzki
标识
DOI:10.1021/acs.jpclett.2c03855
摘要
Application of femtosecond time-resolved transient absorption spectroscopy on all-trans and central-cis isomers of two exemplary carotenoids, lutein and spirilloxanthin, performed at room and cryogenic temperatures in the spectral range expanded toward UV revealed new spectroscopic transient features for the cis isomers. Notably, particularly for the central-cis spirilloxanthin, a very distinct additional transient absorption band is observed on the short wavelength side of the main excited-state absorption band of the S1 state, having the same temporal characteristics as the latter one. This band is absent in transient absorption spectra of all-trans isomers, suggesting it could be assigned to "transient cis-peak." Overall, the results show that the "transient" counterpart of the spectral marker of cis-isomers of carotenoids, or the so-called cis-peak, is detectable in the excited-state absorption spectrum and could be attributed to electronic transition from the S1 state. This new transient spectral band could be very useful for spectroscopic experiments targeting the dynamics of carotenoid isomers and their severely distorted forms.
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