In ref. 8, B-values were determined by using polymer-bound RB (Sensitox). The insoluble sensitizer did not allow to determine R by extrapolation to zero sensitizer concentration thus leading to too small kr-values (especially in CC14) and, consequently, to a too large dipole moment for the transitio
Photooxygenation of tetramethylallene competing (2+2) cycloaddition and ene-reactions with singlet oxygen
โ Scribed by Klaus Gollnick; Albert Schnatterer
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 256 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The photooxygenation of 2,4-dimethyl-1,3-pentadiene (1) path, leading to the allylic hydroperoxide 3) are explained by competition between a concerted and a perepoxide was investigated in seven polar and nonpolar solvents by oxygen-uptake measurements. The overall deactivation rate mechanism. In all
Although it is well established that aliphatic amines may quench singlet oxygen,' it has recently been shown that certain amines did react with singlet oxygen to yield specific products.2c'3 There have been several reports of photooxygenation of amines, in which a-oxidation,3c,5 6-oxidation,6 dehydr
## Abstract The reaction of singlet oxygen with 2โphenylnorbornene (**1**) in aprotic solvents gives 3โformylcyclopentyl phenyl ketone (**2**) (10%) and uncharacterized polymer (90%). When methanol is used as solvent, __endo__โ2โphenylโ__exo__โ2โmethoxyโ__exo__โ3โhydroperoxynorbornane (**4**) and _