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dc.contributor.authorMclldowie, M.J.
dc.contributor.authorMocerino, Mauro
dc.contributor.authorOgden, Mark
dc.contributor.authorSkelton, B.
dc.contributor.authorWhite, A.H.
dc.date.accessioned2017-01-30T11:36:49Z
dc.date.available2017-01-30T11:36:49Z
dc.date.created2015-08-23T20:00:40Z
dc.date.issued2015
dc.identifier.citationMclldowie, M.J. and Mocerino, M. and Ogden, M. and Skelton, B. and White, A.H. 2015. C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 82: pp. 47-51.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/13394
dc.identifier.doi10.1007/s10847-015-0525-8
dc.description.abstract

The synthesis of a C4 dissymmetric resorcinarene tetracarboxylic acid derivative and determination of its critical micelle concentration is reported. The tetrahydroxy derivative was prepared by reduction of the tetra-acid. The low-temperature single crystal X-ray structure of the methyl ester derivative of the tetra-acid is also reported. This crystallised with two independent molecules of similar boat (flattened cone) conformation within the asymmetric unit.

dc.publisherSpringer Netherlands
dc.subjectMicelles
dc.subjectResorcinarene
dc.subjectC4 Dissymmetry
dc.subjectCrystal structure
dc.titleC4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
dc.typeJournal Article
dcterms.source.volume82
dcterms.source.startPage47
dcterms.source.endPage51
dcterms.source.issn1388-3127
dcterms.source.titleJournal of Inclusion Phenomena and Macrocyclic Chemistry
curtin.note

The final publication is available at Springer via http://doi.org/10.1007/s10847-015-0525-8

curtin.departmentDepartment of Chemistry
curtin.accessStatusOpen access


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