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Cyclodextrin Complexation of the Stilbene 4-(2-(4-tert-Butylphenyl)ethen-1-yl)benzoate and the Self-assembly of Molecular Devices

dc.contributor.authorLock, Julia Siobhan
dc.contributor.authorMay, Bruce L
dc.contributor.authorClements, Philip
dc.contributor.authorLincoln, Stephen F
dc.contributor.authorEaston, Christopher
dc.date.accessioned2015-12-13T22:40:19Z
dc.date.available2015-12-13T22:40:19Z
dc.date.issued2004
dc.date.updated2015-12-11T09:55:03Z
dc.description.abstractE-4-(2-(4-tert-butylphenyl)ethen-1-yl)benzoate, E-1-, photoisomerizes to the Z-1- isomer and vice versa in the free state and in the binary complexes 2·E-1-, 2·Z-1-, 3·E-1- and 3·Z-1- where 2 is the urea-linked cyclodextrin N-(6A-deoxy-α-cyclodextrin
dc.identifier.issn0923-0750
dc.identifier.urihttp://hdl.handle.net/1885/78183
dc.publisherKluwer Academic Publishers
dc.sourceJournal of Inclusion Phenomena and Macrocyclic Chemistry
dc.subjectKeywords: cyclodextrin; stilbene 4 [2 (4 tert butylphenyl)ethen 1 yl]benzoate; stilbene derivative; unclassified drug; complex formation; conference paper; isomer; isomerism; molecular dynamics Complexation; Cyclodextrin; Molecular device; Photoisomerization
dc.titleCyclodextrin Complexation of the Stilbene 4-(2-(4-tert-Butylphenyl)ethen-1-yl)benzoate and the Self-assembly of Molecular Devices
dc.typeJournal article
local.bibliographicCitation.issue1
local.bibliographicCitation.lastpage18
local.bibliographicCitation.startpage13
local.contributor.affiliationLock, Julia Siobhan, University of Adelaide
local.contributor.affiliationMay, Bruce L, University of Adelaide
local.contributor.affiliationClements, Philip, University of Adelaide
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidEaston, Christopher, u9500570
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030302 - Nanochemistry and Supramolecular Chemistry
local.identifier.ariespublicationMigratedxPub6865
local.identifier.citationvolume50
local.identifier.doi10.1007/s10847-003-8829-5
local.identifier.scopusID2-s2.0-12344255773
local.type.statusPublished Version

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