Picosecond and nanosecond studies of the photoreduction of benzophenone by N,N-diethylaniline and triethylamine
- Univ. of Notre Dame, IN (United States)
The photoreduction of benzophenone by N,N-diethylaniline and triethylamine has been examined in a number of solvents by both nano- and picosecond laser photolysis. With diethylaniline, electron transfer is the primary step and the spectrum of the ion pair has been detected even in nonpolar solvents such as benzene and cyclohexane. Rapid proton transfer then takes place to form a high yield of the ketyl radical. The lifetime of the ion pair in benzene is about 900 ps. In acetonitrile, the ion pair dissociated into individual ions which then decay by back electron transfer and proton transfer. A spectral shift to the red occurs over 100 ps as the contact ion pair dissociated. In acidic alcohols such as methanol and trifluoroethanol, proton transfer from the alcohol occurs to produce the ketyl radical. In the case of triethylamine, no distinct absorption band for benzophenone anion was seen in picosecond experiments but difference spectra, which removed much of the spectrum of benzophenone triplet, clearly showed some contribution from the anion. For this compound, it is likely that electron transfer occurs first followed by very fast proton transfer.
- OSTI ID:
- 5156751
- Journal Information:
- Journal of Physical Chemistry; (United States), Vol. 95:19; ISSN 0022-3654
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
BENZOPHENONE
PHOTOCHEMICAL REACTIONS
REDUCTION
ABSORPTION SPECTROSCOPY
ALKYLATED AROMATICS
AMINES
ANIONS
CATIONS
ELECTRON TRANSFER
EXPERIMENTAL DATA
ION PAIRS
IONS
PROTONS
RADICALS
SOLVENTS
TIME DEPENDENCE
TIME RESOLUTION
VISIBLE SPECTRA
AROMATICS
BARYONS
CHARGED PARTICLES
CHEMICAL REACTIONS
DATA
ELEMENTARY PARTICLES
FERMIONS
HADRONS
INFORMATION
KETONES
NUCLEONS
NUMERICAL DATA
ORGANIC COMPOUNDS
RESOLUTION
SPECTRA
SPECTROSCOPY
TIMING PROPERTIES
400500* - Photochemistry