1994
DOI: 10.1007/bf02061138
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Stable products and radicals in the radiolysis of dichloromethane and 1,1,-dichloroethane gamma-irradiated in an oxygen-free atmosphere

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Cited by 8 publications
(4 citation statements)
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“…Therefore, the interaction found with chlorine is likely to be one of the most important processes in explaining the stable behavior of astatine in chloroform upon evaporation. Radiolysis of dichloromethane also form a number of radiolysis products where chlorine atoms are intermediate products 46 , providing an explanation to the similar evaporation stability found in this solvent. Di-halogen and di-halogen binary astatine compounds such as AtI/AtBr and AtI 2 − /AtBr 2 − as well as a ternary halogen compound (IAtBr − ) have previously been shown to exist in aqueous solution 47 .…”
Section: Resultsmentioning
confidence: 77%
“…Therefore, the interaction found with chlorine is likely to be one of the most important processes in explaining the stable behavior of astatine in chloroform upon evaporation. Radiolysis of dichloromethane also form a number of radiolysis products where chlorine atoms are intermediate products 46 , providing an explanation to the similar evaporation stability found in this solvent. Di-halogen and di-halogen binary astatine compounds such as AtI/AtBr and AtI 2 − /AtBr 2 − as well as a ternary halogen compound (IAtBr − ) have previously been shown to exist in aqueous solution 47 .…”
Section: Resultsmentioning
confidence: 77%
“…Unfortunately, this is not possible when considering dichloromethane radiolysis. Indeed, gamma-irradiation of dichloromethane leads to the generation of several transient species and stable products, such as (1, 1-dichloroethane, 1,2-dichloroethane, 1,1,2-trichloroethane and 1,1,2, 2-tetrachloroethane), which absorb light in the wavelength range 230-400 nm (Truszkowski and Szymański, 1994), causing an overlap with the absorption of 3HT as already observed in case of EDOT monomers (Bahry et al, 2018(Bahry et al, , 2020. Thus, in the present experimental conditions in dichloromethane solvent, it is not possible to determine in this way the initial radiolytic yield of 3HT oxidation, G ox , nor the irradiation dose, D max , needed for quantitative polymerization of 10 mM in 3HT monomers according to equation (2).…”
Section: Dose Effect Study Under N 2 and O 2 Atmospheresmentioning
confidence: 99%
“…Indeed, it has been demonstrated in the literature that the products of dichloromethane radiolysis in an oxygen-free atmosphere, namely (1,1-dichloroethane, 1,2-dichloroethane, 1,1,2-trichloroethane and 1,1,2,2-tetrachloroethane), absorb light between 230 and 400 nm. 31 This evidently prevents the direct study of EDOT decay.…”
Section: Radiation Induced Synthesis Of Pedot and Dose Effect Studymentioning
confidence: 99%