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dc.contributor.authorCui, X.
dc.contributor.authorRohl, Andrew
dc.contributor.authorShtukenberg, A.
dc.contributor.authorKahr, B.
dc.date.accessioned2017-01-30T13:49:56Z
dc.date.available2017-01-30T13:49:56Z
dc.date.created2013-04-01T20:00:48Z
dc.date.issued2013
dc.identifier.citationCui, Xiaoyan and Rohl, Andrew L. and Shtukenberg, Alexander and Kahr, Bart. 2013. Twisted Aspirin Crystals. Journal of the American Chemical Society. 135 (9): pp. 3395-3398.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/35478
dc.identifier.doi10.1021/ja400833r
dc.description.abstract

Banded spherulites of aspirin have been crystallized from the melt in the presence of salicylic acid either generated from aspirin decomposition or added deliberately (2.6–35.9 mol %). Scanning electron microscopy, X-ray diffraction analysis, and optical polarimetry show that the spherulites are composed of helicoidal crystallites twisted along the <010> growth directions. Mueller matrix imaging reveals radial oscillations in not only linear birefringence, but also circular birefringence, whose origin is explained through slight (~1.3°) but systematic splaying of individual lamellae in the film. Strain associated with the replacement of aspirin molecules by salicylic acid molecules in the crystal structure is computed to be large enough to work as the driving force for the twisting of crystallites.

dc.publisherThe American Chemical Society
dc.titleTwisted Aspirin Crystals
dc.typeJournal Article
dcterms.source.volume135
dcterms.source.startPage3395
dcterms.source.endPage3398
dcterms.source.issn0001-4842
dcterms.source.titleJournal of the American Chemical Society
curtin.department
curtin.accessStatusFulltext not available


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