Abstract
Fourier transform EPR spectroscopy was employed in studying the electron transfer (ET) and the quenching mechanisms of the photoexcited triplet state of C60 (electron donor) in the presence of the electron acceptor tetracyanoethylene (TCNE) in a benzonitrile solution. The ET reaction product, which is the stable anion radical TCNE•-, interacts with 3C60 (both detected by EPR in the liquid phase), leading to chemically induced dynamic electron polarization of TCNE-, via triplet-doublet mixing mechanism.
Original language | English (US) |
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Pages (from-to) | 7444-7447 |
Number of pages | 4 |
Journal | Journal of physical chemistry |
Volume | 98 |
Issue number | 31 |
DOIs | |
State | Published - Jan 1 1994 |