Related Experiment Video
Updated: Aug 15, 2026

Inactivation of Pathogens via Visible-Light Photolysis of Riboflavin-5′-Phosphate
Published on: April 6, 2022
[Isolation and structure identification of the main photolysis product in vitamin K1]
1Department of Pharmaceutical Analysis, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Objective:
To isolate and identify an unknown photolysis product in Vitamin K1.
Methods:
A column chromatography method was used to prepare the impurity, and spectrometric analyses of ultraviolet spectrum, infrared spectrum, mass spectrum and nuclear magnetic resonance spectrum were carried out to identify its structure.
Results:
Its structure is 2-methyl-3-(3-hydroxy-3, 7, 11, 15-tetramethyl-1-hexadecenyl)-1, 4-naphthoquinone.
Conclusion:
The structure of the photolysis product has been identified.
Related Concept Videos
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview
Photosystem I
Both these photosystems work in concert. An excited electron from PSII is relayed to PSI via an electron transport chain in the thylakoid membrane of the chloroplast, which is comprised of the carrier molecule plastoquinone, the dual-protein cytochrome complex, and plastocyanin. As electrons move between PSII and PSI, they lose energy and must be re-energized...
Photosystem II
The pigment molecules are arranged across two photosystem domains — the antenna complex and the reaction center. The main aim of the pigment molecules...
Photosystems
Functioning of Photosystems
Photosystems contain many pigment molecules, such as chlorophylls and carotenoids, arranged in a particular organization across two domains — the antenna complex and the reaction center. The main aim of the pigment molecules...
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
