{"title":"Structure property relationship study on new cubane-1,4-dicarboxylic acid derivatives","authors":"G. Bényei, Istvan Jalsovszki, K. Fodor-csorba","doi":"10.1117/12.581058","DOIUrl":null,"url":null,"abstract":"Three new series of cubane-1,4-dicarboxylic acid derivatives have been prepared as bis[(4'-alkyl)phenyl]cubane-1,4-dicarboxylates, bis[(4'-alkoxy)phenyl]cubane-1,4-dicarboxylates, and two chiral derivatives as bis(cholestenyl)cubane-1,4-dicarboxylate and (S)- bis{4'-[(2-methylbutyl)oxycarbonyl}phenyl}cubane-1,4-dicarboxylate. These ester type compounds have the bulky cubane skeleton as a central building block in their core system. The lower homologues of the alkoxyphenyl ester series exhibited nematic, the higher ones smectic A phase. The mesophase formation was supressed in case of the (4-alkyl)phenyl- and chiral derivatives.","PeriodicalId":132866,"journal":{"name":"Liquid crystals (Print)","volume":"39 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Liquid crystals (Print)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/12.581058","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Three new series of cubane-1,4-dicarboxylic acid derivatives have been prepared as bis[(4'-alkyl)phenyl]cubane-1,4-dicarboxylates, bis[(4'-alkoxy)phenyl]cubane-1,4-dicarboxylates, and two chiral derivatives as bis(cholestenyl)cubane-1,4-dicarboxylate and (S)- bis{4'-[(2-methylbutyl)oxycarbonyl}phenyl}cubane-1,4-dicarboxylate. These ester type compounds have the bulky cubane skeleton as a central building block in their core system. The lower homologues of the alkoxyphenyl ester series exhibited nematic, the higher ones smectic A phase. The mesophase formation was supressed in case of the (4-alkyl)phenyl- and chiral derivatives.