{"title":"甲基罗丹宁互变异构的理论研究","authors":"G. Baryshnikov, B. Minaev, V. Minaeva","doi":"10.1109/MSMW.2010.5546071","DOIUrl":null,"url":null,"abstract":"Rhodanines is non-aromatic heterocyclic compounds, which are basis for the synthesis of some sensitizing dyes. In papers [1, 2] reported that rhodanine cycle can exist in three tautomeric forms - ketone, enol and thioenol. This is a consequence of large polar N-H bond in rhodanine cycle. Enol and thioenol forms can exist in two equivalent conformations, different in the direction of S-H and O-H bonds (Fig. 1). This conclusion was confirming by the data [2].","PeriodicalId":129834,"journal":{"name":"2010 INTERNATIONAL KHARKOV SYMPOSIUM ON PHYSICS AND ENGINEERING OF MICROWAVES, MILLIMETER AND SUBMILLIMETER WAVES","volume":"22 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2010-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Theoretical study of methylidene rhodanine tautomerism\",\"authors\":\"G. Baryshnikov, B. Minaev, V. Minaeva\",\"doi\":\"10.1109/MSMW.2010.5546071\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Rhodanines is non-aromatic heterocyclic compounds, which are basis for the synthesis of some sensitizing dyes. In papers [1, 2] reported that rhodanine cycle can exist in three tautomeric forms - ketone, enol and thioenol. This is a consequence of large polar N-H bond in rhodanine cycle. Enol and thioenol forms can exist in two equivalent conformations, different in the direction of S-H and O-H bonds (Fig. 1). This conclusion was confirming by the data [2].\",\"PeriodicalId\":129834,\"journal\":{\"name\":\"2010 INTERNATIONAL KHARKOV SYMPOSIUM ON PHYSICS AND ENGINEERING OF MICROWAVES, MILLIMETER AND SUBMILLIMETER WAVES\",\"volume\":\"22 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-06-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2010 INTERNATIONAL KHARKOV SYMPOSIUM ON PHYSICS AND ENGINEERING OF MICROWAVES, MILLIMETER AND SUBMILLIMETER WAVES\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/MSMW.2010.5546071\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2010 INTERNATIONAL KHARKOV SYMPOSIUM ON PHYSICS AND ENGINEERING OF MICROWAVES, MILLIMETER AND SUBMILLIMETER WAVES","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MSMW.2010.5546071","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Theoretical study of methylidene rhodanine tautomerism
Rhodanines is non-aromatic heterocyclic compounds, which are basis for the synthesis of some sensitizing dyes. In papers [1, 2] reported that rhodanine cycle can exist in three tautomeric forms - ketone, enol and thioenol. This is a consequence of large polar N-H bond in rhodanine cycle. Enol and thioenol forms can exist in two equivalent conformations, different in the direction of S-H and O-H bonds (Fig. 1). This conclusion was confirming by the data [2].