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dc.contributor.authorAitken, R Alan
dc.contributor.authorInwood, Ryan
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2022-01-05T00:40:46Z
dc.date.available2022-01-05T00:40:46Z
dc.date.issued2021-10-28
dc.identifier271694445
dc.identifierd3c695fd-519d-427e-b934-35c572d41281
dc.identifier85098773814
dc.identifier000604817100001
dc.identifier.citationAitken , R A , Inwood , R & Slawin , A M Z 2021 , ' The X-ray Structures of ( R )-2,2'-Dimethyl-1,1'-binaphthyl and (±)-2-Bromomethyl-2'-dibromomethyl-1,1'-binaphthyl ' , Journal of Chemical Crystallography , vol. 51 , no. 4 , pp. 497-504 . https://doi.org/10.1007/s10870-020-00876-9en
dc.identifier.issn1074-1542
dc.identifier.otherORCID: /0000-0002-9527-6418/work/86537557
dc.identifier.otherORCID: /0000-0001-6959-5311/work/86538043
dc.identifier.urihttps://hdl.handle.net/10023/24594
dc.descriptionWe would like to thank the Engineering and Physical Sciences Research Council and CRITICAT Centre for Doctoral Training for financial support [Grant Code: EP/L016419/1].en
dc.description.abstractMolecular structures of (R)-2,2'-dimethyl-1,1'-binaphthyl [monoclinic, a = 11.24420 (11), b = 10.56190 (9), c = 13.27180 (13) Å, β = 90.7041 (9)º, space group P21] and (±)-2-bromomethyl-2'-dibromomethyl-1,1'-binaphthyl [triclinic, a = 9.4637 (14), b = 9.9721 (18), c = 9.9922 (19) Å, α = 100.093 (5), β = 97.141 (5), γ = 92.585 (4)º, space group P-1] are reported and compared with those of other simple 2,2'-disubstituted-1,1'-binaphthyls.
dc.format.extent8
dc.format.extent3128017
dc.language.isoeng
dc.relation.ispartofJournal of Chemical Crystallographyen
dc.subjectBinaphthylen
dc.subjectTorsion angleen
dc.subjectInter-ring bond lengthen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleThe X-ray Structures of (R)-2,2'-Dimethyl-1,1'-binaphthyl and (±)-2-Bromomethyl-2'-dibromomethyl-1,1'-binaphthylen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1007/s10870-020-00876-9
dc.description.statusPeer revieweden
dc.date.embargoedUntil2022-01-05
dc.identifier.grantnumberEP/L016419/1en


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