1966
DOI: 10.1021/j100879a507
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Isomeric Transition Induced Reactions of Iodine-130 in Cyclohexane

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Cited by 7 publications
(9 citation statements)
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“…One striking feature of iodine reactions was that yields and product distributions of 130 I and 128 I activated by (IT) and (η, γ) processes, respectively, were similar to yields and analogous product distributions of 82 Br activated by (IT) events in cyclohexane and other C 5 -C e hydrocarbons [3,4]. The likeness between l;o I, 128 I and 82 Br yields and product distributions suggest that activated halogens may trace chemical processes which result from a similarity of environmental activation and/or decomposition [4,5].…”
Section: Introductionmentioning
confidence: 91%
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“…One striking feature of iodine reactions was that yields and product distributions of 130 I and 128 I activated by (IT) and (η, γ) processes, respectively, were similar to yields and analogous product distributions of 82 Br activated by (IT) events in cyclohexane and other C 5 -C e hydrocarbons [3,4]. The likeness between l;o I, 128 I and 82 Br yields and product distributions suggest that activated halogens may trace chemical processes which result from a similarity of environmental activation and/or decomposition [4,5].…”
Section: Introductionmentioning
confidence: 91%
“…One striking feature of iodine reactions was that yields and product distributions of 130 I and 128 I activated by (IT) and (η, γ) processes, respectively, were similar to yields and analogous product distributions of 82 Br activated by (IT) events in cyclohexane and other C 5 -C e hydrocarbons [3,4]. The likeness between l;o I, 128 I and 82 Br yields and product distributions suggest that activated halogens may trace chemical processes which result from a similarity of environmental activation and/or decomposition [4,5]. The study of iodine reactions in various halogen substituted methanes is interesting because these mono-carbon compounds, containing, in some cases, no carbon-hydrogen bonds, present environments to the activated iodine that are highly dissimilar to hydrocarbons with respect to bond energies, molecular dimensions, and stability of potential products.…”
Section: Introductionmentioning
confidence: 91%
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“…An atom undergoing isomeric transition 4+ in CH.,1 must be charged to I or higher for the atoms to obtain the 7.1 eV kinetic energy required to displace H from OL. of CH 4 and I activated by (n,y), (n,r) + (IT), and (IT) processes are shown in Figures 11, 13, and 15, respectively. The Xe extrapolated value ( Fig.…”
Section: Determination Of Isomeric Transition Induced Organic Yieldsmentioning
confidence: 99%
“…An interesting phenomena found in going from single carbon methane to multi carbon molecules was that the organic yield drastically decreased. See Table XXXVIII The following exothermic ion molecule reactions can take place for C~H fi or C,Hg but not for CH 4 due to its relatively high ionization potential;…”
Section: A Recent Condensed Phase Studymentioning
confidence: 99%