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

被引:133
|
作者
Saha, Binoy K.
Nangia, Ashwini [1 ]
Nicoud, Jean-Francois
机构
[1] Univ Hyderabad, Sch Chem, Hyderabad 500046, Andhra Pradesh, India
[2] CNRS, Inst Phys & Chim Mat Strasbourg, Grp Mat Organ, Strasbourg 2, France
[3] Univ Strasbourg 1, UMR 7504, Strasbourg 2, France
关键词
D O I
10.1021/cg060117k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 (mu) halogenated N-oxides 2 (mu>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.
引用
收藏
页码:1278 / 1281
页数:4
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