R. Alder, K. R. Anderson, P. Benjes, C. Butts, P. Koutentis, A. Orpen
{"title":"具有横向芳香基团和严格控制的链构象的聚合物和低聚物","authors":"R. Alder, K. R. Anderson, P. Benjes, C. Butts, P. Koutentis, A. Orpen","doi":"10.1039/A707389E","DOIUrl":null,"url":null,"abstract":"Anionic ring-opening polymerisation of spiro[cyclopropane-1,9′-fluorene] with fluorenyl anion as initiator yields polymers 1 with chains which are essentially all-anti and have transversely-oriented fluorenyl groups, as shown by strong upfield shifts for the mid-chain methylene and 1,8-fluorenyl protons; synthetic routes to some specific oligomers are also reported.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"77 1","pages":"309-310"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"12","resultStr":"{\"title\":\"Polymers and oligomers with transverse aromatic groups and tightly controlled chain conformations\",\"authors\":\"R. Alder, K. R. Anderson, P. Benjes, C. Butts, P. Koutentis, A. Orpen\",\"doi\":\"10.1039/A707389E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Anionic ring-opening polymerisation of spiro[cyclopropane-1,9′-fluorene] with fluorenyl anion as initiator yields polymers 1 with chains which are essentially all-anti and have transversely-oriented fluorenyl groups, as shown by strong upfield shifts for the mid-chain methylene and 1,8-fluorenyl protons; synthetic routes to some specific oligomers are also reported.\",\"PeriodicalId\":17282,\"journal\":{\"name\":\"Journal of The Chemical Society, Chemical Communications\",\"volume\":\"77 1\",\"pages\":\"309-310\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society, Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/A707389E\",\"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, Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/A707389E","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Polymers and oligomers with transverse aromatic groups and tightly controlled chain conformations
Anionic ring-opening polymerisation of spiro[cyclopropane-1,9′-fluorene] with fluorenyl anion as initiator yields polymers 1 with chains which are essentially all-anti and have transversely-oriented fluorenyl groups, as shown by strong upfield shifts for the mid-chain methylene and 1,8-fluorenyl protons; synthetic routes to some specific oligomers are also reported.