Photoreduction of Triplet Benzophenone by Tertiary Amines: Amine molecular structure and ketyl radical yield
- 12 May 1997
- journal article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 80 (3), 719-724
- https://doi.org/10.1002/hlca.19970800309
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Photoinduced electron transfer between triethylamine and aromatic carbonyl compounds: the role of the nature of the lowest triplet stateJournal of the Chemical Society, Faraday Transactions, 1996
- Marcus inverted region: nature of donor–acceptor pairs and free ion yieldsJournal of the Chemical Society, Faraday Transactions, 1994
- Comparative electron-transfer quenching rates of 9,10-dicyanoanthracene by various donors in solvents of different polaritiesJournal of the Chemical Society, Faraday Transactions, 1993
- Photostabilization mechanisms of hindered amine light stabilizers: interaction of singlet and triplet anthracene with piperidine model compoundsJournal of Photochemistry and Photobiology A: Chemistry, 1992
- Triisopropylamin, ein sterisch überfülltes Molekül mit eingeebneter NC3‐Pyramide und einem p‐Typ‐StickstoffelektronenpaarAngewandte Chemie, 1991
- Proton affinities and ionization energies of bicyclic amines and diamines. Effects of ring strain and of 3-electron .sigma. bondingJournal of the American Chemical Society, 1981
- Picosecond dynamics of the photoreduction of benzophenone by triethylamineJournal of the American Chemical Society, 1980
- Primary quantum yields of ketyl radicals in photoreduction by amines. Abstraction of hydrogen from nitrogenJournal of the American Chemical Society, 1980
- Quantitative proton affinities, ionization potentials, and hydrogen affinities of alkylaminesJournal of the American Chemical Society, 1976
- Bicyclo[3.3.3.]undecane and 1-azabicyclo[3.3.3]undecane. Geometry, strain, and spectroscopic behavior of these systemsJournal of the American Chemical Society, 1972