Cookies Policy

This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies.

I accept this policy

Find out more here

Comparison of Photoinduced Electron Transfer Reactions of C60 and Aromatic Carbonyl Compounds

No metrics data to plot.
The attempt to load metrics for this article has failed.
The attempt to plot a graph for these metrics has failed.
The full text of this article is not currently available.

Brill’s MyBook program is exclusively available on BrillOnline Books and Journals. Students and scholars affiliated with an institution that has purchased a Brill E-Book on the BrillOnline platform automatically have access to the MyBook option for the title(s) acquired by the Library. Brill MyBook is a print-on-demand paperback copy which is sold at a favorably uniform low price.

This Article is currently unavailable for purchase.
Add to Favorites
You must be logged in to use this functionality

Cover image Placeholder

The one-electron reduction potential of the triplet excited state of C60 is similar to those of some aromatic carbonyl compounds. Thus, photoinduced electron transfer is expected to occur from the common electron donors to both C60 and aromatic carbonyl compounds. In this paper comparison is made between photoinduced electron transfer from organosilanes and organostannanes used as the electron donors to the triplet excited states of C60 and aromatic carbonyl compounds, providing valuable insight into their common mechanistic features for the C-C bond formation via photoinduced electron transfer as well as the new functionalization method of C60.

Affiliations: 1: Department of Applied Chemistry, Faculty ofEngineering, Osaka University, Suita, Osaka 565, Japan


Full text loading...


Data & Media loading...

Article metrics loading...



Can't access your account?
  • Key

  • Full access
  • Open Access
  • Partial/No accessInformation