Propyl iodide, photolysis

The lack of laser action in the photolysis of isopropyl iodide raises intriguing questions. As Husain and Donovan point out, this does not necessarily indicate the absence of population inversion, since under the laser experimental conditions there could instead be an insufficient absolute concentration of I atoms. Spectroscopic studies show that excited iodine atoms are produced from isopropyl iodide photodissociation, but at lower relative concentrations than for n-propyl iodide under similar conditions. Since the two propyl iodides show similar I quenching rates, it would appear most likely that a decreased I /I ratio is the reason stimulated emission is not seen. The present experiments, unfortunately, cannot provide a more quantitative explanation. The distinct broadness of the isopropyl iodide distribution in fig. 2 indicates a departure from the methyl- ethyln-propyl trend, and might represent comparable amounts of P and I atom production, with overlapping translational energy distributions, at least when viewed with our present... 

A series of other halogenated compounds have been identihed in seawater, including ethyl iodide, propyl iodide, bromoiodomethane, chloro-iodomethane, and di-iodomethane (Carpenter et al., 2000 Klick and Abrahamsson, 1992). Little is known about their production mechanisms. Loss mechanisms are likely to include photolysis and reaction with chloride and hydroxide ions. Information is too limited to be used to derive global fluxes for these compounds, although the data available indicate that a reasonable case can be made that the iodine flux from these compounds is similar to that from CH3I. 

Other photolysis studies have been reported for ethyl iodide -propyl iodide and isopropyl iodide in the gas phase, and also in liquid and solu-tion . Solution and liquid phase studies have also been reported for butyl ° , pentyl and cetyl iodides ". The primary process in the photolysis of alkyl iodides has been further discussed by Donovan and Husain in reference to the formation of excited halogen atoms. 

As mentioned briefly in Chapter 5, the photodimerization of acenaphthylene is subject to a very interesting heavy-atom solvent effect. The results of the photolysis of acenaphthylene in some heavy-atom solvents are given in Table 10.6.<4a) The data in Table 10.6 show that the heavy-atom solvents n-propyl bromide and ethyl iodide yield product ratios similar to that obtained in the sensitized photolysis, indicating a greater role of the triplet state in... 

In order to determine the sensitivity of coumarin dimerization to heavy-atom perturbation, the direct photolysis was carried out in butyl chloride, propyl bromide, and ethyl iodide. Comparison of these results with those obtained in nonpolar solvents indicated that there was no significant change in the amount of the triplet-derived product (80) formed in the heavy-atom solvents as would be expected if heavy-atom perturbation were important.<90) More recent investigations,<93W however, of the formation of (79) in carbon tetrachloride indicate that halocarbon enhancement of the formation of this isomer exists. A direct measure of the intersystem quantum... 

In an attempt to detect alkyl radicals spectroscopically, Thrush168 carried out the flash photolysis of ethyl, propyl, and isopropyl iodides... 

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