Photoinduced electron transfer from triplet fullerene, [sup 3]C[sub 60], to tetracyanoethylene. Fourier transform electron paramagnetic resonance study

Journal Article · Thu Aug 04 00:00:00 EDT 1994 · Journal of Physical Chemistry; (United States)

DOI:https://doi.org/10.1021/j100082a008· OSTI ID:6970709

Michaeli, S; Meiklyar, V; Levanon, H ^[1]; Schulz, M; Moebius, K ^[2]

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1. Hebrew Univ., Jerusalem (Israel)
2. Free Univ., Berlin (Germany)

Fourier transform EPR spectroscopy was employed in studying the electron transfer (ET) and the quenching mechanisms of the photoexcited triplet state of C[sub 60] (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[sup [minus]], interacts with [sup 3]C[sub 60] (both detected by EPR in the liquid phase), leading to chemically induced dynamic electron polarization of TCNE[sup [minus]], via triplet-doublet mixing mechanism. 30 refs., 3 figs., 1 tab.

• OSTI ID: 6970709
• Journal Information: Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 98:31; ISSN JPCHAX; ISSN 0022-3654
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400102 -- Chemical & Spectral Procedures
400201* -- Chemical & Physicochemical Properties
400500 -- Photochemistry
CARBON
DISPERSIONS
ELECTRON SPIN RESONANCE
ELECTRON TRANSFER
ELEMENTS
ENERGY LEVELS
EXCITED STATES
FULLERENES
LASERS
MAGNETIC RESONANCE
MIXTURES
MULTIPLETS
NITRILES
NONMETALS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
RADICALS
RESONANCE
SOLUTIONS
TRIPLETS