The bimolecular rate constants for electron transfer from aromatic triplets to polyaryl carbocations are large and diffusioncontrolled even in the limit of high exothermicity. In some cases, although the exothermicity of energy transfer is comparable to that for electron transfer, the latter dominat
Triplet-triplet energy transfer from aromatic to saturated compounds
β Scribed by V.A. Smirnov; V.B. Nazarov; V.I. Gerko; M.V. Alfimov
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 276 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Enerm transfer from the upper triplet states of aromatic compounds to saturated compounds at 77 K has been inves-@ted.
Positions of triplet states of saturated molecules have been estimated in the ranges: 47800-48450 cm-' for methylcyclohexane, ethylcyclohexane, ethanol and ether, 47320-47800 cm -t for isopropylcyclohexane and tran~deulin, and 48450-50000 cm-1 for isooctane.
The radius of the energy transfer sphere for biphenylAIO and t~~ns-dec&in is found to be 5.1 A. It is assumed that energy transfer occurs faster than vibrational relaxa'ton.
π SIMILAR VOLUMES
## Abstract The excited electronic states of 2, 2βdimethylisoindene (1) have been studied by electronβenergyβloss spectroscopy. Its vertical gasβphase triplet (1^3^B~2~), and singlet (1^1^B~2~) excitation energies are 1.61 and 3.19 eV, respectively. The excited states are thus lowered by 0.49 eV an