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Beevers structure

N. Walker and C. J. Beevers, A Fatigue Crack Closure Mechanism in Titanium , Fatigue of Engineering Materials and Structures, Wo[. 1, 1979, pp. 135 148. [Pg.533]

Beevers, C. A. and Schwarz, C. M. (1935). The crystal structure of nickel sulphate heptahydrate NiS04- 7H2O. Zeit. Kristallogr. 91, 157-69. [Pg.254]

Beevers, C. A. The crystal structure of dicalcium phosphate dihydrate, CaHPC>4 2 H2O. Acta Cryst. 11, 273-277 (1958). [Pg.91]

The degradation work had up to this point occupied itself mainly with the proof of the gross skeletal structure, and relatively little attention had been given to the stereochemistry of the molecule. It was at this point that this aspect of the problem was cleared by the determination of the structure of strychnine by X-ray crystallographic analysis independently by Robertson and Beevers (35) and Bijvoet et al. (36). [Pg.598]

C. A. Beevers and A. F. Trotman-Dickenson. Acta Cryst. 10, 34-7 (1957). Grys-tsU structure nitramide. [Pg.392]

Beevers, C. A., and Hughes, W. The crystal structure of Rochelle salt (sodium potassium tartrate tetrahydrate NaKC4H4O6-4H30). Proc. Roy. Soc. (London) A177, 251-259 (1941). [Pg.181]

Beevers, C. A., and Lipson, H. Crystal structure of copper sulphate pentahy-drate, CuS04-5H20. Proc. Roy. Soc. (London) A146, 570-582 (1934). Robertson, J. M. An X-ray study of the structure of the phthalocyanines. Part I. The metal-free, nickel, copper and platinum compounds. J. Chem. Soc. (London) 615-621 (1934). [Pg.341]

Lipson. H., and Beevers, C. A. An improved numerical method of two-dimensional Fourier synthesis for crystals. Proc. Phys. Soc. 48, 772-780 (1936). Patterson, A. L., and Tunell, G. A method for the summation of the Fourier series used in the X-ray analysis of crystal structures. Amer. Mineralogist 27. 655-679 (1942). [Pg.382]

FIG. 13.6. (a) The relation of the structure of 0-alumina, NaAli 1O17, to that of spinel (after Beevers and Ross). Large circles represent Na, small ones O, and black circles Al. (b) The relation of the structure of magneto-plumbite, PbFei jOij, to that of magnetite Fe304 (after Adelskold). Large circles represent Pb, small ones O, and black circles Fe. [Pg.495]

There have been two crystal-structure determinations of myo-inositol, the inositol stereoisomer having only one axial hydroxyl group. One of these studies, by Rabinowitz and Kraut, was on the anhydrous form and the other, by Lomer, Miller, and Beevers, was on the dihydrate. In both structures, the molecules have the expected chair conformation, and the proposal by Posternak of an axial hydroxyl group on C-4 was fully confirmed. The more accurate work on the anhydrous form provided evidence of small deviations, of the order of 1°, from the ideal chair conformation. [Pg.15]

Figure 3.8 The structure of the protein concanavalin-A, a saccharide binding protein, is predominantly p sheet, (a) Beevers molecular model (with permission to be reproduced here). (b) Ribbon diagram (kindly prepared by Dr J. Raftery). Based originally on the coordinates of Reeke, Becker and Edelman (1975). The ribbon representation was introduced by Richardson (1985). The computer program RIBBON was authored by Priestle (1988). Figure 3.8 The structure of the protein concanavalin-A, a saccharide binding protein, is predominantly p sheet, (a) Beevers molecular model (with permission to be reproduced here). (b) Ribbon diagram (kindly prepared by Dr J. Raftery). Based originally on the coordinates of Reeke, Becker and Edelman (1975). The ribbon representation was introduced by Richardson (1985). The computer program RIBBON was authored by Priestle (1988).
Figure 3.18 The Watson-Crick double helical structure of DNA illustrated by the crystal structure of an oligonucleotide. (a) Skeletal model representation, in stereo (note the tilting of the base pairs in certain cases this is responsible for causing the DNA double helix to coil up, for example, into the nucleosome, a key component of the chromosome). (b) Space filling representation, in stereo, (c) Beevers molecular model. Figures kindly provided by Dr W. N. Hunter with permission. Figure 3.18 The Watson-Crick double helical structure of DNA illustrated by the crystal structure of an oligonucleotide. (a) Skeletal model representation, in stereo (note the tilting of the base pairs in certain cases this is responsible for causing the DNA double helix to coil up, for example, into the nucleosome, a key component of the chromosome). (b) Space filling representation, in stereo, (c) Beevers molecular model. Figures kindly provided by Dr W. N. Hunter with permission.
Krahl, Cod, Biochem. Prepn. 1, 33 (1949). Prepn from a-acetobromglucose + silver diphenyl phosphate Postemak. J. Am. Chem. Soc. 72,4824 (1950) by phosphor-olysis of starch using phosphorylase and orthophosphate McCready, Hassid, Biochem. Prepn. 4, 63 (1955). Structure Wolfrom, Pletcher, J. Am. Chem. Soc. 63, 1050 (1941). Configuration Wolfrom et al, ibid. 64, 23 (1942) Harmon, Diss. Abstr. 24, 4400 (1964) Beevers, Maconochie, Acta Cryst. 18, 232 (1965). [Pg.700]

Beevers, C.A., and M.A.S. Ross. 1937. The crystal structure of beta alumina Na20-1 IAI2O3. Zeitschrift fur Kristallogr hie 97 59-66. Bertsch, P.M. 1989. Aqueous polynuclear aluminum species. Pp. 88-111 in The Environmental Chemistry of Aluminum, G. Sposito (ed.). [Pg.104]

Robinson C, Ward JC, Beevers RB (1958) Liquid crystalline structure in polypeptide solutions. Part 2. Discuss Earaday Soc 25 29-42... [Pg.196]


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