Thermal expansion of β-succinic acid and α-adipic acid in relation to their crystal structures

The thermal expansion quadrics of β -succinic acid and α -adipic acid have been determined by X-ray Weissenberg method. In adipic acid, X-ray measurements have been made between —100 and +100°C and in succinic acid between —150 and +130°C. In these monoclinic crystals, the minimum expansion corresponds to the c axis, which coincides with the direction of the hydrogen-bonded molecular columns. In other directions along which van der Waals forces prevail, thermal expansion is greater, being maximum perpendicular to the (100) planes, the direction of the obtuse bisectrix of the molecular packing angle. The thermal expansion is quantitatively explained by assuming an increase in the angular vibration of the molecules.

1980 ◽  
Vol 35 (1) ◽  
pp. 14-17 ◽  
Author(s):  
Walter Gonschorek

Abstract The molecular and crystal structures of dibrom maleic acid thioanhydride and diiod maleic acid thioanhydride have been determined by means of single-crystal X-ray intensities. The crystal structures are isomorphous and have the space group P41212 (enantiomorphous with P43212). The lattice constants are a = 7.543 Å, c = 12.155 Å (DBMTA) and a = 7.816 Å, c = 12.348 Å (DIMTA). The five-membered rings of the molecules are planar with maximum deviations of 0.003 Å (DBMTA) and 0.005 Å (DIMTA). Adjacent molecules are held together by van-der-Waals-forces.


Polyhedron ◽  
2005 ◽  
Vol 24 (8) ◽  
pp. 865-871 ◽  
Author(s):  
Mohan S. Bharara ◽  
Chong H. Kim ◽  
Sean Parkin ◽  
David A. Atwood

1987 ◽  
Vol 40 (7) ◽  
pp. 1147 ◽  
Author(s):  
EJ Oreilly ◽  
G Smith ◽  
CHL Kennard ◽  
TCW Mak

The crystal structures of (2-formyl-6-methoxyphenoxy)acetic acid (1), diaquabis [(2-formyl-6-methoxyphenoxy) acetato ]zinc(11) (2), tetraaquabis [(2-chlorophenoxy) acetato ]zinc(11) (3), triaquabis [(2-chlorophenoxy) acetato ]cadmium(11) dihydrate (4) and lithium (2-chloro- phenoxy )acetate 1.5 hydrate (5) have been determined by X-ray diffraction. The acid (1) forms centrosymmetric hydrogen-bonded cyclic dimers [O…0, 2.677(6) �] which are non-planar. Complex (2) is six-coordinate with two waters [Zn- Ow , 1.997(2) �] and four oxygens from two asymmetric bidentate carboxyl groups [Zn-O, 2.073, 2.381(2) �] completing a skew trapezoidal bipyramidal stereochemistry. Complex (5) is also six-coordinate but is octahedral, with two trans-related unidentate carboxyl oxygens [mean Zn-O, 2.134(9) �] and four waters [mean Zn-O, 2.081(9) �]. The seven-coordinate complex (4) has crystallographic twofold rotational symmetry relating two :symmetric bidentate acid ligands [ Cd -O, 2.26, 2 48(:) �] and two waters [ Cd -O, 2.34(2) �] while the third water lies on this axis [ Cd -O, 2.27(2) �]. In contrast to the monomers (2)-(4), complex (5) is polymeric with tetrahedral lithium coordinated to one water and three carboxylate oxygens [mean Li-0, 1.95(1) �]. The essential conformation of the free acid is retained in complexes (2), (3) and (4) but in (5), it is considerably changed.


Author(s):  
C. J. Birkett Clews ◽  
F. Schoszberger ◽  
William Lawrence Bragg

Investigations of the micellar structure of fibre substances have given rise to two theories. The older theory (Meyer and Mark 1930; Mark 1932; Siefriz 1934; Meyer 1930; and Nageli 1928) considers the micelles as separate crystallites, between which lie the intermicellar spaces. The micelles consist of “Hauptvalenzketten” bound together along their length by homeopolar bonds and in the transverse direction by van der Waals’ forces, the intermicellar binding being also attributed to van der Waals’ forces. The original model suggested in work published by K. H. Meyer (1930), for cellulose, depicts the micelles arranged like bricks in a wall (fig. 1), and doubtless this is the simplest explanation of the X-ray results. But it is difficult to understand how such an arrangement can give a micellar structure its peculiar mechanical properties, and further how it is possible, when both inter- and intramicellar cohesion are attributed to the same type of force, to cause by swelling experiments an enlargement of the intermicellar spaces, while the “Hauptvalenzketten” remain unaffected. An alternative theory has been put forward by O. Gerngross, K. Herrmann and W. Abitz (1930), W. T. Astbury (1933), A. Frey-Wyssling (1936) and E. Guth and S. Rogowin (1936). These authors suppose that a given “Hauptvalenzkette” is not confined to a single crystalline region but may stretch through more such regions. In general, the arrangement of the neighbouring chains will be truly lattice-like, but a chain may lie at too great a distance from its neighbours or not lie exactly parallel to them, so that the structure as a whole will show statistically distributed spaces. In fig. 2 ordered crystalline regions may be distinguished (drawn in thick line), but their significance is physically different from that of the crystallites of the Meyer model. They are not self-contained units; the whole system is linked together due to the “Hauptvalenzketten” extending beyond a single micelle. Astbury considers that in a substance of high molecular weight of a type capable of swelling that part which produces the X-ray spectrum is the concentration centre of a complicated network of thread-like molecules. He draws an analogy between micellar structure and the secondary structure of Zwicky. He suggests that it is possible that micellar systems, which are characterized by a mixture of perfection and imperfection, are the counterpart in compounds of high molecular weight of the well-known mosaic structure of the more familiar crystals. Frey-Wyssling is of the opinion that the micelles, growing together, enclose lens-shaped spaces running parallel to the fibre axis. Between these intermicellar spaces are small rod-shaped regions of undistorted lattice, which are the so-called micelles of the earlier work (fig. 3). In this figure, which gives a pictorial representation of Frey’s theory, the statistically distributed hollow spaces are shown black; some of these are enclosed in undistorted crystalline regions. A lamellar structure consisting of superimposed monomolecular layers suggested by O. L. Sponsler and W. H. Dore (1930) has been shown to be untenable from the work on double refraction by Baas-Becking and Galliher (1931).


1938 ◽  
Vol 11 (3) ◽  
pp. 510-514
Author(s):  
C. J. B. Clews ◽  
F. Schossberger

Abstract Investigations of the micellar structure of fiber substances have given rise to two theories. The older theory (Meyer and Mark, 1930; Mark, 1932; Siefriz, 1934; Meyer, 1930; and Nägeli, 1928) considers the micelles as separate crystallites, between which lie the intermicellar spaces. The micelles consist of “Hauptvalenzketten“ bound together along their length by homeopolar bonds and in the transverse direction by van der Waals' forces, the intermicellar binding being also attributed to van der Waals' forces. The original model suggested in work published by Meyer (1930) for cellulose depicts the micelles arranged like bricks in a wall (Fig. 1), and doubtless this is the simplest explanation of the x-ray results. But it is difficult to understand how such an arrangement can give a micellar structure its peculiar mechanical properties, and further how it is possible, when both inter- and intramicellar cohesion are attributed to the same type of force, to cause by swelling experiments an enlargement of the intermicellar spaces, while the “Hauptvalenzketten” remain unaffected.


CrystEngComm ◽  
2015 ◽  
Vol 17 (4) ◽  
pp. 753-763 ◽  
Author(s):  
German L. Perlovich ◽  
Alex M. Ryzhakov ◽  
Valery V. Tkachev ◽  
Alexey N. Proshin

The crystal structures of six adamantane derivatives of sulfonamides have been determined by X-ray diffraction and their sublimation and fusion processes have been studied.


Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5691
Author(s):  
Cyprian M. Chunkang ◽  
Iris E. Ikome ◽  
Emmanuel N. Nfor ◽  
Yuta Mitani ◽  
Natsuki Katsuumi ◽  
...  

Single crystals of two achiral and planar heterocyclic compounds, C9H8H3O(CA1) and C8H5NO2 (CA4), recrystallized from ethanol, were characterized by single crystal X-ray analysis, respectively, and chiral crystallization was observed only for CA1 as P212121 (# 19), whereas it was not observed for CA4 P21/c (# 14). In CA1, as a monohydrate, the hydrogen bonds were pronounced around the water of crystallization (O4), and the planar cyclic sites were arranged in parallel to slightly tilted positions. On the other hand, an anhydride CA4 formed a dimer by hydrogen bonds between adjacent molecules in the crystal, which were aggregated by van der Waals forces and placed in parallel planar cyclic sites.


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