1964
DOI: 10.1080/00268976300101401
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A hydrocarbon trinegative ion

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1965
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Cited by 12 publications
(1 citation statement)
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“…The radical cations of hexamethylbenzene and pentamethylbenzene have been characterized by Hulme and Symons (168,169) and are more or less as expected, the latter cations exhibiting a spectrum in which the o-methyl groups are split by the onep-methyl. Decacyclene (50) and tetracene (246) have yielded trianions due to high electron affinities. The barrier to internal rotation for stilbene anion-radical was found to be 9.0 kcal.…”
Section: Multiple Quantum Transitions In O•mentioning
confidence: 99%
“…The radical cations of hexamethylbenzene and pentamethylbenzene have been characterized by Hulme and Symons (168,169) and are more or less as expected, the latter cations exhibiting a spectrum in which the o-methyl groups are split by the onep-methyl. Decacyclene (50) and tetracene (246) have yielded trianions due to high electron affinities. The barrier to internal rotation for stilbene anion-radical was found to be 9.0 kcal.…”
Section: Multiple Quantum Transitions In O•mentioning
confidence: 99%