International
Tables for
Crystallography
Volume B
Reciprocal space
Edited by U. Shmueli

International Tables for Crystallography (2006). Vol. B. ch. 4.4, p. 462   | 1 | 2 |

Section 4.4.4.3.2. Crystal-G, crystal-J

P. S. Pershana*

aDivision of Engineering and Applied Science and The Physics Department, Harvard University, Cambridge, MA 02138, USA
Correspondence e-mail: pershan@deas.harvard.edu

4.4.4.3.2. Crystal-G, crystal-J

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The crystalline-G and crystalline-J phases are the ordered versions of the smectic-F and smectic-I phases, respectively. The positions of the principal peaks illustrated in Fig. 4.4.4.4[link] for the smectic-F(I) are identical to the positions in the smectic-G(J) phase if small thermal shifts are discounted. In both the hexatic and the crystalline phases, the molecules are tilted with respect to the layer normals by approximately 25 to 30° with nearly hexagonal packing around the tilted axis (Doucet & Levelut, 1977[link]; Levelut et al., 1974[link]; Levelut, 1976[link]; Leadbetter, Mazid & Kelly, 1979[link]; Sirota, Pershan, Sorensen & Collett, 1987[link]). The interlayer molecular packing appears to be end to end, in an AAA type of stacking (Benattar et al., 1983[link]; Benattar et al., 1981[link]; Levelut, 1976[link]; Gane et al., 1983[link]). There is only one molecule per unit cell and there is no evidence for the long-wavelength modulations that are so prevalent in the crystalline-B phase that is the next higher temperature phase above the crystalline-G in 7O.7.

References

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First citation Doucet, J. & Levelut, A. M. (1977). X-ray study of the ordered smectic phases in some benzylideneanilines. J. Phys. (Paris), 38, 1163–1170.Google Scholar
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