{"title":"用碳-13傅里叶变换核磁共振直接观察水中两种形态的水氰酸","authors":"D. Doddrell, A. Allerhand","doi":"10.1039/C29710000728","DOIUrl":null,"url":null,"abstract":"Proton-decoupled natural-abundance carbon-13 Fourier transform n.m.r. spectra of aqueous solutions of aquocyanocobyric acid and dicyanocobyric acid were recorded at 15·08 MHz: the spectrum of the first compound showed the presence of two isomers, and many of the carbon atoms showed large chemical shift variations between the two isomers.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"64 1","pages":"728-729"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Direct observation of the two forms of aquocyanocobyric acid in water by carbon-13 Fourier transform nuclear magnetic resonance\",\"authors\":\"D. Doddrell, A. Allerhand\",\"doi\":\"10.1039/C29710000728\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Proton-decoupled natural-abundance carbon-13 Fourier transform n.m.r. spectra of aqueous solutions of aquocyanocobyric acid and dicyanocobyric acid were recorded at 15·08 MHz: the spectrum of the first compound showed the presence of two isomers, and many of the carbon atoms showed large chemical shift variations between the two isomers.\",\"PeriodicalId\":17278,\"journal\":{\"name\":\"Journal of The Chemical Society D: Chemical Communications\",\"volume\":\"64 1\",\"pages\":\"728-729\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society D: Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C29710000728\",\"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 The Chemical Society D: Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C29710000728","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Direct observation of the two forms of aquocyanocobyric acid in water by carbon-13 Fourier transform nuclear magnetic resonance
Proton-decoupled natural-abundance carbon-13 Fourier transform n.m.r. spectra of aqueous solutions of aquocyanocobyric acid and dicyanocobyric acid were recorded at 15·08 MHz: the spectrum of the first compound showed the presence of two isomers, and many of the carbon atoms showed large chemical shift variations between the two isomers.
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