Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/94200
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dc.titlemeso-2,2,2′,2′-Tetrachloro-1,1′-diphenyl-1,1′- bicyclopropyl and meso-2,2,2′,2′-Tetrabromo-1,1′-diphenyl-1,1′- bicyclopropyl
dc.contributor.authorLam, Y.-L.
dc.contributor.authorKoh, L.-L.
dc.contributor.authorHuang, H.-H.
dc.date.accessioned2014-10-16T08:33:18Z
dc.date.available2014-10-16T08:33:18Z
dc.date.issued1997-04-15
dc.identifier.citationLam, Y.-L.,Koh, L.-L.,Huang, H.-H. (1997-04-15). meso-2,2,2′,2′-Tetrachloro-1,1′-diphenyl-1,1′- bicyclopropyl and meso-2,2,2′,2′-Tetrabromo-1,1′-diphenyl-1,1′- bicyclopropyl. Acta Crystallographica Section C: Crystal Structure Communications 53 (4) : 499-504. ScholarBank@NUS Repository.
dc.identifier.issn01082701
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94200
dc.description.abstractMolecules of meso-2,2,2′,2′-tetrachloro-1,1′-diphenyl-1,1′- bicyclopropyl, C18H14Cl4, (1), and meso-2,2,2′,2′-tetrabromo-1,1′-diphenyl-1,1′- bicyclopropyl, C18H14Br4, (2), adopt gauche conformations. Compound (1) produced two types of crystals upon recrystallization. The phenyl rings of the two forms of compound (1), as well as those of compound (2), are in a nearly perpendicular orientation. All three structures have unsymmetrical cyclopropane rings, with the shortest C-C bond being between the rings at the point of phenyl substitution.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleActa Crystallographica Section C: Crystal Structure Communications
dc.description.volume53
dc.description.issue4
dc.description.page499-504
dc.description.codenACSCE
dc.identifier.isiutNOT_IN_WOS
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