{"title":"Mass spectrometry of quinones. Part II. A study of the distinguishing features found in the mass spectra of 1,2- and 1,4-naphthaquinones","authors":"R. Oliver, R. Rashman","doi":"10.1039/J29710000341","DOIUrl":null,"url":null,"abstract":"The mass spectra of 18 variously substituted 1,2-naphthaquinones are reported and discussed. It is shown that the majority of the ortho-naphthaquinones studied are reduced by water vapour present in the mass spectrometer and that this reaction provides a mass spectral method for distinguishing between 1,2- and 1,4-naphthaquinones. No simple relationship is found to exist between the solution redox potentials and the ease of reduction of the 1,2-naphthaquinones in the spectrometer. Finally, fragmentation patterns for the individual quinones studied are suggested and these are correlated with the type and position of the substituent in the quinone nucleus.","PeriodicalId":17268,"journal":{"name":"Journal of The Chemical Society B: Physical Organic","volume":"25 1","pages":"341-344"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society B: Physical Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J29710000341","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
The mass spectra of 18 variously substituted 1,2-naphthaquinones are reported and discussed. It is shown that the majority of the ortho-naphthaquinones studied are reduced by water vapour present in the mass spectrometer and that this reaction provides a mass spectral method for distinguishing between 1,2- and 1,4-naphthaquinones. No simple relationship is found to exist between the solution redox potentials and the ease of reduction of the 1,2-naphthaquinones in the spectrometer. Finally, fragmentation patterns for the individual quinones studied are suggested and these are correlated with the type and position of the substituent in the quinone nucleus.