{"title":"多环芳烃的新型氧化剂周期酸。","authors":"A. Fatiadi","doi":"10.1039/C19670001087","DOIUrl":null,"url":null,"abstract":"Certain polycyclic, aromatic hydrocarbons can be oxidized with periodic acid in aprotic solvents containing a small proportion of water. A unique, two-fold character of response to periodic acid by these hydrocarbons has been found: (1) production of a coupling reaction through a radical intermediate [conversion of pyrene into 1,1'-bipyrene, and fluorene into 1,2-bis(2,2'-biphenylylene)ethylene] or (2) conversion into quinones by a two-equivalent oxidation mechanism that does not involve a radical intermediate [acenaphthene, anthracene, anthrone, benz[a]anthracene, naphthacene, naphthalene, and phenanthrene]. Little or no reaction was observed when oxidation was attempted with sodium metaperiodate instead of periodic acid. Electron-spin resonance revealed no radical intermediate in the oxidation of malonic acid with either periodic acid or sodium periodate.","PeriodicalId":94340,"journal":{"name":"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry","volume":"10 1","pages":"341-350"},"PeriodicalIF":0.0000,"publicationDate":"1968-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Periodic Acid, a Novel Oxidant of Polycyclic, Aromatic Hydrocarbons.\",\"authors\":\"A. Fatiadi\",\"doi\":\"10.1039/C19670001087\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Certain polycyclic, aromatic hydrocarbons can be oxidized with periodic acid in aprotic solvents containing a small proportion of water. A unique, two-fold character of response to periodic acid by these hydrocarbons has been found: (1) production of a coupling reaction through a radical intermediate [conversion of pyrene into 1,1'-bipyrene, and fluorene into 1,2-bis(2,2'-biphenylylene)ethylene] or (2) conversion into quinones by a two-equivalent oxidation mechanism that does not involve a radical intermediate [acenaphthene, anthracene, anthrone, benz[a]anthracene, naphthacene, naphthalene, and phenanthrene]. Little or no reaction was observed when oxidation was attempted with sodium metaperiodate instead of periodic acid. Electron-spin resonance revealed no radical intermediate in the oxidation of malonic acid with either periodic acid or sodium periodate.\",\"PeriodicalId\":94340,\"journal\":{\"name\":\"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry\",\"volume\":\"10 1\",\"pages\":\"341-350\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1968-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C19670001087\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C19670001087","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Periodic Acid, a Novel Oxidant of Polycyclic, Aromatic Hydrocarbons.
Certain polycyclic, aromatic hydrocarbons can be oxidized with periodic acid in aprotic solvents containing a small proportion of water. A unique, two-fold character of response to periodic acid by these hydrocarbons has been found: (1) production of a coupling reaction through a radical intermediate [conversion of pyrene into 1,1'-bipyrene, and fluorene into 1,2-bis(2,2'-biphenylylene)ethylene] or (2) conversion into quinones by a two-equivalent oxidation mechanism that does not involve a radical intermediate [acenaphthene, anthracene, anthrone, benz[a]anthracene, naphthacene, naphthalene, and phenanthrene]. Little or no reaction was observed when oxidation was attempted with sodium metaperiodate instead of periodic acid. Electron-spin resonance revealed no radical intermediate in the oxidation of malonic acid with either periodic acid or sodium periodate.