@misc{oai:repo.qst.go.jp:00070335,
 author = {Nakanishi, Ikuo and Ohkubo, Kei and Kawashima, Tomonori and Inami, Keiko and Matsumoto, Kenichiro and Fukuhara, Kiyoshi and Okuda, Haruhiro and Mochizuki, Masataka and Fukuzumi, Shunichi and Ozawa, Toshihiko and Anzai, Kazunori and 中西 郁夫 and 川島 知憲 and 松本 謙一郎},
 month = {Nov},
 note = {The phenolate anion derived from a vitamin E model, 2,2,5,7,8-pentamethylchroman-6-ol (PMC), in the presence of a strong base is reported to reduce molecular oxygen to generate superoxide anion, one of reactive oxygen species, in acetonitrile (MeCN) (Org. Biomol. Chem. 1:4085; 2003).  However, very little is known about the detailed electron-transfer properties of phenolate anions derived from phenolic antioxidants.  In this study, we report the PMC anion can act as a strong electron donor to 2,2-diphenyl-1-picrylhydrazyl radical as well as to a series of p-benzoquinones in MeCN.  The kinetic data obtained in this study were evaluated in light of the Marcus theory of electron transfer, providing valuable insight into the electron-transfer properties of the phenolate anions derived from phenolic antioxidants., SFRBM/SFRRI 2010},
 title = {Electron-Transfer Properties of the Phenolate Anion Derived from a Vitamin E Model in the Presence of a Strong Base in an Aprotic Medium},
 year = {2010}
}