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E. Kosower (1958)
The Effect of Solvent on Spectra. I. A New Empirical Measure of Solvent Polarity: Z-ValuesJournal of the American Chemical Society, 80
H. Hanson, F. Herman, J. Lea, S. Skillman (1964)
HFS atomic scattering factorsActa Crystallographica, 17
E. Kosower (1958)
The Effect of Solvent on Spectra. II. Correlation of Spectral Absorption Data with Z-ValuesJournal of the American Chemical Society, 80
E. Kosower (1958)
The Effect of Solvent on Spectra. III. The Use of Z-Values in Connection with Kinetic DataJournal of the American Chemical Society, 80
Seiki Sakanoue, N. Yasuoka, N. Kasai, M. Kakudo, S. Kusabayashi, H. Mikawa (1969)
The Crystal Structure of an Organic Charge Transfer Salt, [2(C9H8N)+·(C10N6)2−]Bulletin of the Chemical Society of Japan, 42
The crystal structure of an organic charge-transfer complex, 1-ethyl-2-methylquinolinium iodide, [(C12H14N)+·I−], has been determined by means of three-dimensional X-ray data (MoKα). The crystals are monoclinic, space group P21/c, and have four formula units in a unit cell with the dimensions of a=7.187±0.002, b=15.914±0.002, c=10.331±0.002 Å, and β=94.67±0.01°. The structure is built up from an iodide anion and a planar 1-ethyl-2-methylquinolinium cation, which lie roughly on a plane. The cations are stacked approximately parallel to the a-plane, forming an endless column along the a axis; the interplanar spacings of these cations are alternately 3.4 and 3.6 Å. The iodide anions are located in the spaces between these columns and the ethyl groups of the cations. The closest distance between an iodide anion and the carbon atoms of a 1-ethyl-2-methylquinolinium ring is 3.93 Å.
Bulletin of the Chemical Society of Japan – Oxford University Press
Published: Mar 27, 2006
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