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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 29 (1999), S. 1043-1048 
    ISSN: 1572-8854
    Keywords: arene–arene contacts ; quadrupole interactions ; intermolecular interactions ; iodine–iodine interactions ; nonlinear optics ; azines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract 4-Iodoacetophenone azine crystallizes in the space group Pbcn with cell parametersa = 34.5187(19), b = 7.2638(4), and c = 6.3736(3) Å. The azine shows a gauche conformation with regard to the N—N bond and the phenyl rings are twisted in a way that leads to the largest possible twist between the benzene rings of each azine. This azine conformation allows for intermolecular arene–arene T-contacts between pairs of benzene rings and these double-T contacts involve only molecules within the same layer. All azines are perfectly colinear within each layer and this results in a quadrilateral kite-shaped arrangement of iodine atoms at the interface of each layer. The iodine-iodine distances within each layer are 4.5 and 5.1 Å, and the three unique angles of the kite-shaped quadrilaterals are 97.1, 76.9, and 88.8°. The iodine atoms in adjacent layers pack such that atoms of one layer fill the square interstices of the next layer. The distances between iodine atoms in adjacent layers are 4.5 and 4.1 Å. The C—I bonds are not orthogonal to the I-planes and the direction of the molecules in adjacent layers causes a deviation of about 40° from colinearity
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8854
    Keywords: Dipole parallel-alignment ; anisotropy ; arene–arene contacts ; intermolecular interactions ; nonlinear optics ; azines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound crystallizes in the space group Pna2(1) with cell parameters a = 6.4606(3), b = 7.2155(3) and c = 33.5878(16) Å. The azine shows a gauche conformation about the N—N bond and there is an angle of 58.1° between the benzene rings of each azine. This conformation allows for two intermolecular arene–arene T-contacts between pairs of benzene rings. The characteristic structural motif features T-contact formation between like–substituted arene rings and this architecture results in a highly dipole-parallel aligned lattice. All azines are perfectly colinear within each layer and the orientations of the azines in different layers are nearly the same. The surfaces of the layers exhibit a quadrilateral kite-shaped arrangement of I-atoms and of OCH3-substituents. The layers pack such that the OCH3—carbon atoms are placed above the interstices between the I-atoms in the adjacent layer.
    Type of Medium: Electronic Resource
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