Using halogen⋯halogen interactions to direct noncentrosymmetric crystal packing in dipolar organic molecules

dc.contributor.author Saha, Binoy K.
dc.contributor.author Nangia, Ashwini
dc.contributor.author Nicoud, Jean François
dc.date.accessioned 2022-03-27T09:30:01Z
dc.date.available 2022-03-27T09:30:01Z
dc.date.issued 2006-06-01
dc.description.abstract Halogen atoms Cl, Br, and I steer crystallization of 2-halo-3- hydroxypyridine 1, pyridine-N-oxides 2, and 2-halo-3-aminopyridine 3 in noncentrosymmetric space groups efficient for nonlinear optical materials. Whereas the strong hydrogen-bond chains are aligned antiparallel, the L- or V-geometry of weak interhalogen interaction steers polar alignment in the solid state, even for high dipole moment (μ) halogenated N-oxides 2 (μ > 5.0 D). Six out of seven structures evaluated crystallize in polar/chiral space groups due to interhalogen interactions compared to the one in six probability of noncentrosymmetric packing for achiral molecules. © 2006 American Chemical Society.
dc.identifier.citation Crystal Growth and Design. v.6(6)
dc.identifier.issn 15287483
dc.identifier.uri 10.1021/cg060117k
dc.identifier.uri https://pubs.acs.org/doi/10.1021/cg060117k
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12981
dc.title Using halogen⋯halogen interactions to direct noncentrosymmetric crystal packing in dipolar organic molecules
dc.type Journal. Article
dspace.entity.type
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