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A color version of the Hinsberg test: permethylated cyclodextrin and crown-appended azophenol for highly selective sensing of amines

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dc.contributor.authorJung, Jong Hwa-
dc.contributor.authorLee, Hye Young-
dc.contributor.authorJung, Sung Ho-
dc.contributor.authorLee, Soo Jin-
dc.contributor.authorSakata, Yoshiteru-
dc.contributor.authorKaneda, Takahiro-
dc.date.accessioned2022-12-27T06:07:21Z-
dc.date.available2022-12-27T06:07:21Z-
dc.date.issued2008-07-07-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/27343-
dc.description.abstractAzophenol dyes 1-5 having the permethylated cyclodextrin and/OF crown moieties have been synthesized. Compounds 1 and 2 provide critical information for discrimination among 1 degrees-3 degrees amines by unique color changes. Addition of 1 degrees and 2 degrees amines to solutions of I or 2 in chloroform shifts the absorbance maximum of the initial solutions from 380 nm to similar to 580 nm and similar to 530 nm, respectively, but no change is observed with 3 degrees amines. The high selectivity of I is mainly due to H-bonding between the ammonium H atoms of the amine and oxygen atoms of the crown-6. The selectivity of 1 possessing the beta-cycloclextrin moiety toward amines was higher than that of 2 possessing the alpha-cyclodextrin moiety. On the other hand, chloroform solutions of 3 or 4, which lack the crown ether moiety, changed from yellow (380 nm) to pink (500 nm) with the addition of 1 degrees and 2 degrees amines, but with no selectivity. These results indicate that the crown unit in 1 or 2 plays an important role in discriminating among the types of amines. (C) 2008 Elsevier Ltd. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleA color version of the Hinsberg test: permethylated cyclodextrin and crown-appended azophenol for highly selective sensing of amines-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.tet.2008.05.013-
dc.identifier.scopusid2-s2.0-45449094166-
dc.identifier.wosid000257500500014-
dc.identifier.bibliographicCitationTETRAHEDRON, v.64, no.28, pp 6705 - 6710-
dc.citation.titleTETRAHEDRON-
dc.citation.volume64-
dc.citation.number28-
dc.citation.startPage6705-
dc.citation.endPage6710-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusAMMONIA-
dc.subject.keywordPlusSENSOR-
dc.subject.keywordPlusDYE-
dc.subject.keywordAuthoralanines-
dc.subject.keywordAuthoramphiphiles-
dc.subject.keywordAuthorhelical ribbons-
dc.subject.keywordAuthorself-assembly-
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