Enantiospecific inclusion of chiral 1,2-dichloroethane rotamers in the crystal lattice of chiral square-pyramidal Cu(II) complexes with perfectly polar alignment of guest and host molecules

dc.contributor.author Muppidi, Vamsee Krishna
dc.contributor.author Zacharias, Panthapally S.
dc.contributor.author Pal, Samudranil
dc.date.accessioned 2022-03-27T08:47:18Z
dc.date.available 2022-03-27T08:47:18Z
dc.date.issued 2005-05-21
dc.description.abstract The inclusion compounds, [CuL12(H2O)] ·(P)-C2H4Cl2 and [CuL22(H2O)]·(M)-C2H4Cl 2 (HL1 = N-(2-hydroxy-5-nitrobenzyl)-(-R)-α- methylbenzylamine and HL2 = N-(2-hydroxy-5-nitrobenzyl)-(S)-α- methylbenzylamine), crystallise in the non-centrosymmetric space group C2; intermolecular hydrogen bonding leads to a perfectly polar alignment of both host and guest molecules with enantioselectivity. © The Royal Society of Chemistry 2005.
dc.identifier.citation Chemical Communications
dc.identifier.issn 13597345
dc.identifier.uri 10.1039/b501642h
dc.identifier.uri http://xlink.rsc.org/?DOI=b501642h
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11785
dc.title Enantiospecific inclusion of chiral 1,2-dichloroethane rotamers in the crystal lattice of chiral square-pyramidal Cu(II) complexes with perfectly polar alignment of guest and host molecules
dc.type Journal. Article
dspace.entity.type
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