{"title":"乙酰丙酸在有机和水-有机溶液中氧化还原性能的电化学研究","authors":"G. V. Burmakina","doi":"10.17516/1998-2836-0246","DOIUrl":null,"url":null,"abstract":"The redox properties of levulinic acid (LA) were studied by electrochemical methods in acetonitrile, a mixture of acetonitrile with water, ethanol, acetone, and dimethyl sulfoxide. It was shown that the irreversible two-electron reduction of LA under the studied conditions leads to the formation of γ-valerolactone. This reduction potential depends on the solvent and shifted anodically by following order: dimethyl sulfoxide","PeriodicalId":16999,"journal":{"name":"Journal of Siberian Federal University. Chemistry","volume":null,"pages":null},"PeriodicalIF":0.5000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Electrochemical Study of the Redox Properties of Levulinic Acid in Organic and Aqueous-Organic Solutions\",\"authors\":\"G. V. Burmakina\",\"doi\":\"10.17516/1998-2836-0246\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The redox properties of levulinic acid (LA) were studied by electrochemical methods in acetonitrile, a mixture of acetonitrile with water, ethanol, acetone, and dimethyl sulfoxide. It was shown that the irreversible two-electron reduction of LA under the studied conditions leads to the formation of γ-valerolactone. This reduction potential depends on the solvent and shifted anodically by following order: dimethyl sulfoxide\",\"PeriodicalId\":16999,\"journal\":{\"name\":\"Journal of Siberian Federal University. Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2021-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Siberian Federal University. Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17516/1998-2836-0246\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Siberian Federal University. Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17516/1998-2836-0246","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemical Study of the Redox Properties of Levulinic Acid in Organic and Aqueous-Organic Solutions
The redox properties of levulinic acid (LA) were studied by electrochemical methods in acetonitrile, a mixture of acetonitrile with water, ethanol, acetone, and dimethyl sulfoxide. It was shown that the irreversible two-electron reduction of LA under the studied conditions leads to the formation of γ-valerolactone. This reduction potential depends on the solvent and shifted anodically by following order: dimethyl sulfoxide
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