The Crystalline Structure of Poly-β,D(1→4′)mannose: Mannan I

1972 ◽  
Vol 50 (13) ◽  
pp. 2130-2138 ◽  
Author(s):  
I. Nieduszynski ◽  
R. H. Marchessault

The crystallographic structure of mannan I has been examined by X-ray fiber diffraction, polarized i.r. spectroscopy, and computer chain-packing methods. The combination of X-ray intensity data and the chain packing analyses have shown that the overall number of permissible structures is very limited so that van der Waals' forces play a major role in packing. It was concluded that the chain senses are anti-parallel. The interpretation of the polarized i.r. spectra in the OH stretching region is in line with the presence of an intra-molecular hydrogen-bond between O(3)… O(5′). The awkward "knobby" shape of the mannan molecule, largely a result of the axial disposition of O(2)—H, lends itself to a close packing mainly determined by van der Waals' forces. The considerable similarity between X-ray and i.r. data from mannans and glucomannans would indicate that structural conclusions about the former might relate to the latter.

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).


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.


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.


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.


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.


1952 ◽  
Vol 25 (1) ◽  
pp. 12-14 ◽  
Author(s):  
V. I. Kasatochkin ◽  
B. V. Lukin

Abstract The molecular structure of rubber resembles that of liquids, which have a characteristic distribution of linear-chain molecules, united by transverse van der Waals forces. The x-ray diffraction diagram of undeformed rubber shows a diffuse ring, the characteristic diffraction spectrum of liquids, and this is accepted as experimental proof of the similarity between rubber and liquids. The theory that the structure of rubber involves reactive bonds in the adjacent molecular chains at short distances apart is not in accord with the relatively free rotation of these chains, which is manifest by the elastic properties of rubber, and the theory in no way distinguishes unvulcanized rubber from straight-chain paraffins. A straight-chain molecular system in which most of the links of adjacent chains are cross-bridged by van der Waals forces is a fairly rigid system, with relatively little molecular motion. The rotation of the links is equivalent to rupture of the van der Waals bonds, and in no way corresponds to the observed high degree of motion of the molecular chains in rubber, as reflected in the high elasticity of the latter. The results of the experimental study which is described in the present paper and which is concerned with the x-ray diffraction spectra of amorphous rubber and of rubber which has become crystalline by stretching, lead to the conclusion that amorphous rubber contains fragments of molecular chains, the links of which do not scatter x-rays in the form of an amorphous ring. Futhermore, the experiments offer proof of the absolutely essential role of the above-mentioned molecular structure of rubber in determining a number of properties of the rubber.


1981 ◽  
Vol 36 (2) ◽  
pp. 188-194 ◽  
Author(s):  
Klaus-Peter Jensen ◽  
Dietrich K. Breitinger ◽  
Wolfram Kreß

The X-ray structure analysis of bis(chloromercuri)methane CH2(HgCl)2 has been performed. CH2(HgCl)2 crystallizes in Prnma with a = 713.7(4) pm, b - 643.6(4) pm, c = 1221.7(8) pm, Z = 4; the isotypic CH2(HgBr)2 has a = 731.1(3) pm, b = 668.6(1) pm, c - 1260.1(4) pm. The CH2(HgCl)2 molecules (site symmetry m) contain asymmetric CHg2 entities with bond lengths R(C-Hg(l)) = 203.9(17) pm and R(C-Hg(2)) = 212.2(18) pm, respectively, whereas the two independent Hg-Cl bonds are almost the same (average (Hg-Cl) = 233.3(5) pm). The bond angles Hg-C-Hg (111.6(3)°) and C-Hg-Cl (average 177.8(5)°) fall into the expected range. The molecules are held together by two independent systems of short van der Waals contacts Cl →···Hg forming zig-zag chains along the 6-axis, and a wide variety of van der Waals interactions Cl →···Hg in planes parallel to (010). The arrangements in these planes produce maximum density molecular layers with coordination number six; including the molecules of two adjacent layers each molecule reaches a total coordination number of fourteen. Depending on the van der Waals radius assumed for mercury a packing coefficient 0.663 ≤ k ≤ 0.733 comparable to that of close-packing of spheres results.


1996 ◽  
Vol 61 (5) ◽  
pp. 726-732
Author(s):  
Jaroslav Podlaha ◽  
Ivana Císařová ◽  
Martin Bělohradský ◽  
Jiří Závada

The configuration and conformation of the title compound as a representative of conformationally locked ternaphthyls was determined by single-crystal X-ray diffraction. The arrangement of the mean planes of naphthyl and acetoxy groups results from intramolecular van der Waals forces.


1939 ◽  
Vol 12 (2) ◽  
pp. 119-123
Author(s):  
C. J. B. Clews

Abstract The results of the x-ray study of rubber structure may be summarized as follow : (1) The unit cell is monoclinic, space group C2h5, a=8.53±0.05, b=8.16±0.05, c=12.66±0.05 A˚, β=83°20′, with four isoprene chains in the cis modification passing through the cell, which contains 8 C5H8 residues. (2) In the unstretched state there is a random distribution of ordered crystalline regions and disordered regions. On stretching, the crystalline regions become orientated in one or more crystallographic directions, thereby giving rise to the x-ray fibre diagram. The crystalline regions may be identified with the micelles, which are groups of Hauptvalenzketten bound together by van der Waals' forces; a given Hauptvalenzkette is undoubtedly associated with more than one micelle. It is possible that the abnormal elastic properties are due to the chains becoming aligned parallel to the direction of stretching, and in addition there may be some extension of the chains themselves. Such an effect has been observed by Astbury in his work on keratin. Some recent work on the structure of butadiene and its derivatives in the solid state is described, which, although offering no immediate solution of our problem, may prove of value when further accurate data are available, both for these compounds and for the corresponding rubbers.


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