{"title":"邻双(二氯甲基)苯的旋转受阻","authors":"V. Mark, V. A. Pattison","doi":"10.1039/C29710000553","DOIUrl":null,"url":null,"abstract":"A study of internal rotation in ortho-bis(dichloromethyl)benzenes by 1H n.m.r. spectroscopy shows the presence of locked conformers on the n.m.r. time scale when these substituents are flanked on one or both sides by chlorine of additional dichloromethyl groups, and that in cases where a chlorine is substituted on both sides of two ortho-bis(dichloromethyl)groups ΔG‡ at Tc is 17·4–17·7 kcal mol–1.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"18 1","pages":"553-554"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Hindered rotation in ortho-bis(dichloromethyl)benzenes\",\"authors\":\"V. Mark, V. A. Pattison\",\"doi\":\"10.1039/C29710000553\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A study of internal rotation in ortho-bis(dichloromethyl)benzenes by 1H n.m.r. spectroscopy shows the presence of locked conformers on the n.m.r. time scale when these substituents are flanked on one or both sides by chlorine of additional dichloromethyl groups, and that in cases where a chlorine is substituted on both sides of two ortho-bis(dichloromethyl)groups ΔG‡ at Tc is 17·4–17·7 kcal mol–1.\",\"PeriodicalId\":17278,\"journal\":{\"name\":\"Journal of The Chemical Society D: Chemical Communications\",\"volume\":\"18 1\",\"pages\":\"553-554\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society D: Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C29710000553\",\"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/C29710000553","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Hindered rotation in ortho-bis(dichloromethyl)benzenes
A study of internal rotation in ortho-bis(dichloromethyl)benzenes by 1H n.m.r. spectroscopy shows the presence of locked conformers on the n.m.r. time scale when these substituents are flanked on one or both sides by chlorine of additional dichloromethyl groups, and that in cases where a chlorine is substituted on both sides of two ortho-bis(dichloromethyl)groups ΔG‡ at Tc is 17·4–17·7 kcal mol–1.