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・ Cycloheptane
・ Cycloheptanone
・ Cycloheptatriene
・ Cycloheptene
・ Cyclohexa-1,5-dienecarbonyl-CoA hydratase
・ Cyclohexadiene
・ Cyclohexane
・ Cyclohexane (data page)
・ Cyclohexane conformation
・ Cyclohexane-1,2-diol
・ Cyclohexane-1,2-diol dehydrogenase
・ Cyclohexane-1,2-dione hydrolase
・ Cyclohexane-1,3-dione hydrolase
・ Cyclohexanecarboxylic acid
・ Cyclohexanedimethanol
Cyclohexanehexone
・ Cyclohexanethiol
・ Cyclohexanol
・ Cyclohexanol dehydrogenase
・ Cyclohexanone
・ Cyclohexanone dehydrogenase
・ Cyclohexanone monooxygenase
・ Cyclohexanone oxime
・ Cyclohexene
・ Cyclohexene oxide
・ Cyclohexenone
・ Cycloheximide
・ Cyclohexyl chloride
・ Cyclohexyl nitrite
・ Cyclohexyl-isocyanide hydratase


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Cyclohexanehexone : ウィキペディア英語版
Cyclohexanehexone

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Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C6O6, the sixfold ketone of cyclohexane. It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.
As of May 2006, this compound had yet to be synthesized in bulk.〔

== Related compounds ==

Cyclohexanehexone can be viewed as the neutral counterpart of the rhodizonate anion . The singly charged anion has been detected in mass spectrometry experiments by R. Wyrwas and C. Jarrold, formed by oligomerization of carbon monoxide through the formation of molybdenum carbonyls.
According to X-ray diffraction analysis, the reagent traded under the name "cyclohexanehexone octahydrate" or equivalent names is actually dodecahydroxycyclohexane dihydrate, a solid that decomposes at 95 °C.〔

In 1966, H. E. Worne of Natick Chemical Industries patented compounds with formulas C10O8 and C14O10, which can be described as the fusion of two or three molecules of C6O6, claimed to be produced by the action of ultraviolet radiation on a hot water solution of the parent compound.〔Howard E Worne, "Polycarbonyls", issued Jan 4, 1966〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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