Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/18324
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dc.contributor.authorFrampton, CS-
dc.contributor.authorMcKendrick, JJ-
dc.contributor.authorMacnicol, DD-
dc.date.accessioned2019-06-06T13:07:56Z-
dc.date.available2017-11-01-
dc.date.available2019-06-06T13:07:56Z-
dc.date.issued2017-11-
dc.identifier.citationActa Crystallographica Section E: Crystallographic Communications, 2017, 73 (11), pp. 1662 - 1665en_US
dc.identifier.issn2056-9890-
dc.identifier.issnhttp://dx.doi.org/10.1107/S2056989017014608-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/18324-
dc.description.abstractThe title compound, C22H22OS [systematic name: 4-(1,3,3-trimethyl-2,3-di­hydro-1H-4-thia­phenanthren-1-yl)phenol], crystallizes unsolvated from nitro­methane as colourless prisms (m.p. 425–427 K) in the polar monoclinic space group Ia with Z′ = 2 (mol­ecules A and B). Both independent mol­ecules possess a very similar proximal conformation, this referring to the juxtaposition of the 4-hy­droxy­phenyl substituent with respect to the syn-related methyl group. In the crystal, mol­ecule A is linked to mol­ecule B by an O—H⋯O hydrogen bond. In turn, mol­ecule B exhibits a weak O—H⋯π inter­action with the phenolic group of mol­ecule A related by a-glide symmetry. Together, these lead to [100] chains.en_US
dc.format.extent1662 - 1665-
dc.language.isoenen_US
dc.publisherInternational Union of Crystallographyen_US
dc.subjectcrystal structureen_US
dc.subjectthia-Dianin's compounden_US
dc.subjecthydrogen bondingen_US
dc.title4-(4-Hydroxyphenyl)-2,2,4-trimethyl-7,8-benzothiachroman, a fused-ring counterpart of thia -Dianin's compounden_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1107/S2056989017014608-
dc.relation.isPartOfActa Crystallographica Section E: Crystallographic Communications-
pubs.issue11-
pubs.publication-statusPublished-
pubs.volume73-
Appears in Collections:Dept of Mechanical and Aerospace Engineering Research Papers

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