Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/15256
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFrampton, CS-
dc.contributor.authorMcKendrick, JJ-
dc.contributor.authorMacNicol, DD-
dc.date.accessioned2017-10-11T14:24:14Z-
dc.date.available2017-10-11T14:24:14Z-
dc.date.issued2017-
dc.identifier.citationActa Crystallographica Section Een_US
dc.identifier.issn1600-5368-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/15256-
dc.description.abstractAbstract The title compound, C22H22OS [systematic name 4-(1,3,3-tri­methyl-2,3-di­hydro-1H-4-thia- phenanthren-1-yl)-phenol] crystallizes unsolvated from nitro­methane as colourless prisms m.p. 152–154 °C, 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 p-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··· inter­action with the phenolic group of molecule A related by a-glide symmetry. Together, these lead to [100] chains.en_US
dc.language.isoenen_US
dc.titleCrystal structure of 4-p-hydroxyphenyl-2,2,4-trimethyl-7,8- benzothiachroman: a fused-ring counterpart of thia-Dianin's compound.en_US
dc.typeArticleen_US
dc.relation.isPartOfActa Crystallographica Section E-
pubs.publication-statusAccepted-
Appears in Collections:Dept of Mechanical and Aerospace Engineering Research Papers

Files in This Item:
File Description SizeFormat 
fulltext.pdf1.06 MBAdobe PDFView/Open


Items in BURA are protected by copyright, with all rights reserved, unless otherwise indicated.