{"title":"三乙烯基硼烷与四卤化二硼的反应:一些二卤基硼(乙烯基硼)乙烷的性质","authors":"A. K. Holliday, R. P. Ottley","doi":"10.1039/J19710000886","DOIUrl":null,"url":null,"abstract":"1 : 1 Addition of trivinylborane and diboron tetrachloride gives the adduct 1,2-bis(dichloroboryl)-1-(divinylboryl)-ethane (CH2:CH)2B·CH(BCl2)·CH2BCl2(I), which reacts with BX3(X = Cl, NMe2) to give X2B·CH(BCl2)·CH2BCl2. Dehydroboration of (I) by addition of trimethylamine gives trimethylamine-divinylborane and pyrolysis gives 1,2-bisdichloroborylethylene. Similar 1 : 1 addition using diboron tetrafluoride gives an adduct with properties similar to (I).1 : 2 Addition of trivinylborane and diboron tetrachloride gives (CH2:CH)B[CH(BCl2)·CH2BCl2]2, unstable above –78°C; a similar adduct using diboron tetrafluoride has not been isolated. 1 : 3 addition does not occur with either tetrahalide.","PeriodicalId":17321,"journal":{"name":"Journal of The Chemical Society A: Inorganic, Physical, Theoretical","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Reactions of trivinylborane with diboron tetrahalides: properties of some dihalogenoboryl(vinylboryl)ethanes\",\"authors\":\"A. K. Holliday, R. P. Ottley\",\"doi\":\"10.1039/J19710000886\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"1 : 1 Addition of trivinylborane and diboron tetrachloride gives the adduct 1,2-bis(dichloroboryl)-1-(divinylboryl)-ethane (CH2:CH)2B·CH(BCl2)·CH2BCl2(I), which reacts with BX3(X = Cl, NMe2) to give X2B·CH(BCl2)·CH2BCl2. Dehydroboration of (I) by addition of trimethylamine gives trimethylamine-divinylborane and pyrolysis gives 1,2-bisdichloroborylethylene. Similar 1 : 1 addition using diboron tetrafluoride gives an adduct with properties similar to (I).1 : 2 Addition of trivinylborane and diboron tetrachloride gives (CH2:CH)B[CH(BCl2)·CH2BCl2]2, unstable above –78°C; a similar adduct using diboron tetrafluoride has not been isolated. 1 : 3 addition does not occur with either tetrahalide.\",\"PeriodicalId\":17321,\"journal\":{\"name\":\"Journal of The Chemical Society A: Inorganic, Physical, Theoretical\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society A: Inorganic, Physical, Theoretical\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J19710000886\",\"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 A: Inorganic, Physical, Theoretical","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J19710000886","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Reactions of trivinylborane with diboron tetrahalides: properties of some dihalogenoboryl(vinylboryl)ethanes
1 : 1 Addition of trivinylborane and diboron tetrachloride gives the adduct 1,2-bis(dichloroboryl)-1-(divinylboryl)-ethane (CH2:CH)2B·CH(BCl2)·CH2BCl2(I), which reacts with BX3(X = Cl, NMe2) to give X2B·CH(BCl2)·CH2BCl2. Dehydroboration of (I) by addition of trimethylamine gives trimethylamine-divinylborane and pyrolysis gives 1,2-bisdichloroborylethylene. Similar 1 : 1 addition using diboron tetrafluoride gives an adduct with properties similar to (I).1 : 2 Addition of trivinylborane and diboron tetrachloride gives (CH2:CH)B[CH(BCl2)·CH2BCl2]2, unstable above –78°C; a similar adduct using diboron tetrafluoride has not been isolated. 1 : 3 addition does not occur with either tetrahalide.