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dc.contributor.authorBaynton, A.
dc.contributor.authorOgden, Mark
dc.contributor.authorRaston, C.
dc.contributor.authorJones, Franca
dc.date.accessioned2017-01-30T11:36:40Z
dc.date.available2017-01-30T11:36:40Z
dc.date.created2012-01-19T20:00:32Z
dc.date.issued2012
dc.identifier.citationBaynton, Andrew and Ogden, Mark I. and Raston, Colin L. and Jones, Franca. 2012. Barium sulfate crystallization dependence on upper rim calix[4]arene functional groups. CrystEngComm. 14 (3): pp. 1057-1062.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/13367
dc.identifier.doi10.1039/C1CE06083J
dc.description.abstract

Although the effects of p-sulfonated and p-phosphonated calix[4]arene on barium sulfate morphology are similar, their ability to form mesocrystals of material are markedly different. The p-phosphonated calix[4]arene results in the formation of fibre bundles similar to those previously observed during barium sulfate crystallization in the presence of di-block copolymers. The isostructural sulfonated calix[4]arene, however, affords material consistent with the initial formation of mesocrystals which subsequently fuse. This material shows significant beam damage when viewed under a transmission electron microscope (TEM) suggesting incorporation of the sulfonated calix[4]arene, although there was no evidence of this from X-ray diffraction and atomic force microscopy (AFM) studies. We hypothesise that this calixarene is incorporated without significant change in structure of the material, and that the interaction of the macrocycle with the barium sulfate lattice is sufficiently weak that surface AFM imaging is effective in removing it from the surface.

dc.publisherThe Royal Society of Chemistry
dc.titleBarium sulfate crystallization dependence on upper rim calix[4]arene functional groups
dc.typeJournal Article
dcterms.source.volume14
dcterms.source.number3
dcterms.source.startPage1057
dcterms.source.endPage1062
dcterms.source.issn14668033
dcterms.source.titleCrystEngComm
curtin.departmentNanochemistry Research Institute (Research Institute)
curtin.accessStatusOpen access


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