Document Type
Article
Publication Date
12-14-2016
Publication Title
Membranes
Volume
6
Issue
4
Keywords
Circular dichroism, Methylated tocopherol, Reichardt’s dye, Vitamin E, α-tocopherol, δ-tocopherol
Abstract
We used circular dichroism (CD) to study differences in CD spectra between α-, δ-, and methylated-α-tocopherol in solvents with different polarities. CD spectra of the different tocopherol structures differ from each other in intensity and peak locations, which can be attributed to chromanol substitution and the ability to form hydrogen bonds. In addition, each structure was examined in different polarity solvents using the Reichardt index—a measure of the solvent’s ionizing ability, and a direct measurement of solvent–solute interactions. Differences across solvents indicate that hydrogen bonding is a key contributor to CD spectra at 200 nm. These results are a first step in examining the hydrogen bonding abilities of vitamin E in a lipid bilayer.
DOI
10.3390/membranes6040056
E-ISSN
20770375
Recommended Citation
Marquardt, Drew; Van Oosten, Brad J.; Ghelfi, Mikel; Atkinson, Jeffrey; and Harroun, Thad A.. (2016). Vitamin E circular dichroism studies: Insights into conformational changes induced by the solvent’s polarity. Membranes, 6 (4).
https://scholar.uwindsor.ca/chemistrybiochemistrypub/303