HEAL DSpace

Structure of the 1 : 1 complex of Hexakis(2,3,6-tri-O-methyl) α-Cyclodextrin with (R)-(-)-1,7-Dioxaspiro[5.5]undecane

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dc.contributor.author Mentzafos, D en
dc.contributor.author Mavridis, IM en
dc.contributor.author Yannakopoulou, K en
dc.date.accessioned 2014-06-06T06:44:01Z
dc.date.available 2014-06-06T06:44:01Z
dc.date.issued 1999 en
dc.identifier.issn 09230750 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/1629
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0033099740&partnerID=40&md5=f41d263823c2f801a942e1ed3058e453 en
dc.subject (R)-(-)-1,7-dioxaspiro [5.5]undecane en
dc.subject Chiral recognition en
dc.subject Crystal structure en
dc.subject Hexakis(2,3,6-tri-O-methyl)-α-cyclodextrin en
dc.title Structure of the 1 : 1 complex of Hexakis(2,3,6-tri-O-methyl) α-Cyclodextrin with (R)-(-)-1,7-Dioxaspiro[5.5]undecane en
heal.type journalArticle en
heal.publicationDate 1999 en
heal.abstract The crystal structure of the 1 : 1 inclusion complex of hexakis(2,3,6-tri-O-methyl)-α-cyclodextrin (TMαCD) with 1,7-dioxaspiro[5.5]undecane (spiroacetal) is orthorhombic, space group C2221, with a = 24.002(2), b = 14.812(1), c = 21.792(2) Å, V = 7747.3(11) Å3 and Z = 8. The molecular six-fold axis of TMαCD coincides with the a two-fold crystallographic axis and the guest is located at the secondary methoxy group side, disordered over two positions related by that axis. The guest model used during the refinement is that of the (R)-enantiomer alone because trials to either refine a 1 : 1 mixture of (R)-and (S)-enantiomers or the (S)-enantiomer alone failed. The crystallographic evidence of enantioselectivity towards the (R)-enantiomer of spiroacetal was confirmed by independent experiments and may be attributed to numerous non bonding interactions between host and guest involving non conventional H-bonds. en
heal.journalName Journal of Inclusion Phenomena en
dc.identifier.issue 3 en
dc.identifier.volume 33 en
dc.identifier.spage 321 en
dc.identifier.epage 330 en


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