1-(2,4,6-Triisopropylphenyl)ethanone

Blair, Amber D.; Hendsbee, Arthur D.; Masuda, Jason Douglas, 1977-

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dc.creator	Blair, Amber D.
dc.creator	Hendsbee, Arthur D.
dc.creator	Masuda, Jason Douglas, 1977-
dc.date.accessioned	2018-04-25T13:33:30Z
dc.date.available	2018-04-25T13:33:30Z
dc.date.issued	2011-10
dc.identifier.issn	1600-5368
dc.identifier.uri	http://library2.smu.ca/handle/01/27442
dc.description	Publisher's Version/PDF
dc.description.abstract	The title compound, C<sub>17</sub>H<sub>26</sub>O, is a di-ortho-alkyl substituted phenyl ethanone that exhibits a significant twisting of the ketone fragment relative to the aromatic ring [O—C—C—C torsion angle = 89.32 (17)°] due to steric pressure from the ortho-isopropyl groups. One ortho- and the para-isopropyl group exhibit orientational disorder with a refined site occupancy factor of 0.562 (3):0.438 (3).	en_CA
dc.description.provenance	Submitted by Betty McEachern (betty.mceachern@smu.ca) on 2018-04-25T13:33:30Z No. of bitstreams: 1 Masuda_Jason_D_article_2011_c.pdf: 527239 bytes, checksum: 13d0139a34280adbe05beb06412d6426 (MD5)	en
dc.description.provenance	Made available in DSpace on 2018-04-25T13:33:30Z (GMT). No. of bitstreams: 1 Masuda_Jason_D_article_2011_c.pdf: 527239 bytes, checksum: 13d0139a34280adbe05beb06412d6426 (MD5) Previous issue date: 2011-10	en
dc.language.iso	en	en_CA
dc.publisher	Wiley-Blackwell	en_CA
dc.relation.uri	https://dx.doi.org/10.1107/S1600536811038293
dc.subject.lcsh	Crystallography
dc.subject.lcsh	Organic compounds
dc.subject.lcsh	Organic compounds -- Synthesis
dc.title	1-(2,4,6-Triisopropylphenyl)ethanone	en_CA
dc.type	Text	en_CA
dcterms.bibliographicCitation	Acta Crystallographica E67(10), o2731. (2011)	en_CA