A new polymorph of 2,6-bis(trifluoromethyl)benzoic acid

Masuda, Jason Douglas, 1977-; Giffin, Nick A.; Hendsbee, Arthur D.

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dc.creator	Masuda, Jason Douglas, 1977-
dc.creator	Giffin, Nick A.
dc.creator	Hendsbee, Arthur D.
dc.date.accessioned	2015-07-31T12:49:22Z
dc.date.available	2015-07-31T12:49:22Z
dc.date.issued	2011-05
dc.identifier.issn	1600-5368
dc.identifier.uri	http://library2.smu.ca/xmlui/handle/01/26273
dc.description	Publisher's version/PDF	en_CA
dc.description.abstract	The asymmetric unit of a second polymorph of the title compound, C[subscript 9]H[subscript 4]F[subscript 6]O[subscript 2], contains five independent molecules, which form hydrogen-bonded O—H[ellipsis]O dimers about inversion centers. The most significant structural difference between this structure and that of the first polymorph [Tobin & Masuda (2009). Acta Cryst. E65, o1217] is the hydrogen-bonded, dimeric orientation of the carboxylic acid functionalities.	en_CA
dc.description.provenance	Submitted by Janine Mills (janine.mills@smu.ca) on 2015-07-31T12:49:22Z No. of bitstreams: 1 Masuda_Jason_D_article_2011_a.pdf: 722588 bytes, checksum: 9fc3cdf281d0cfe67ac5881310b48913 (MD5)	en
dc.description.provenance	Made available in DSpace on 2015-07-31T12:49:22Z (GMT). No. of bitstreams: 1 Masuda_Jason_D_article_2011_a.pdf: 722588 bytes, checksum: 9fc3cdf281d0cfe67ac5881310b48913 (MD5) Previous issue date: 2011	en
dc.language.iso	en	en_CA
dc.publisher	International Union of Crystallography	en_CA
dc.relation.uri	http://dx.doi.org/10.1107/S1600536811011731
dc.subject.lcsh	Benzoates
dc.subject.lcsh	Polymorphism (Crystallography)
dc.title	A new polymorph of 2,6-bis(trifluoromethyl)benzoic acid	en_CA
dc.type	Text	en_CA
dcterms.bibliographicCitation	Acta Crystallographica Section E 67, o1054. (2011)	en_CA