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Crystallographic data for some organic compounds

Published online by Cambridge University Press:  14 March 2018

Extract

The isomorphous relationships for organic compounds are not so simple as they sometimes are for inorganic. Very often a series of chemically similar orgallic substances does not show any apparent trace of crystallographic similarity. It appears that the introduction of further groups into the molecule may cause the crystal-system to change in a manner which cannot be predicted. Thus, glyoxalinc-4(or 5)- sulphonic acid is tetragonal, whilst 4(or 5)-bromoglyoxaline-5(or 4)- sulphonic acid is monoclinic; the introduction of a methyl group into the 2 position gives rise to an orthorhombic crystal, whilst the introduction of the same group into the 1 position leaves the crystal-system unchanged. In some cases it has been found that evell though the crystal-system is changed, there still remains a very close similarity between corresponding angles in the different substances.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1925

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References

Page 394 note 1 Barker, T. V., Annual Reports of the Chemical Society, London, 1914, vol. 10 (for 1913), p. 247 Google Scholar ; 1915, vol. 11 (for 1914), p. 24S ; Chem. News, 1912, vol. 106, p. 199; The Lancet, 1917, vol. 1 (for 1917), p. 278; Min. Abstr., ]923, vol. 2, p. I00.

Page 394 note 2 Lapworth, A., Journ. Chem. Soc. London, 1903, Trans. vol. 837 p. 1114 CrossRefGoogle Scholar.

Page 396 note 1 Greenwood, G., Min. Mag., 1923, vol. 20, p. 123 CrossRefGoogle Scholar.

Page 396 note 2 Balaban, I. E. and Pyman, F. L., Journ. Chem. Soc. London, 1924, Trans. vol. 125, p. 1567 CrossRefGoogle Scholar.

Page 397 note 1 Pyman, F. L. and Ravald, L. A., Journ. Chem. Soc. London, 1920, Trans. vol. 117, p. 1430 Google Scholar. The position of the sulphonic acid residue has not been determined with certainty. Compare R. Forsyth, J. A. Moore, and F. L. Pyman, ibid., 1924, vol. 125, p. 919.

Page 398 note 1 Forsyth, R., Moore, J. A., and Pyman, F. L., Journ. Chem. Soc. London, 1924, Trans. vol. 125, p. 921 CrossRefGoogle Scholar.

Page 399 note 1 Ealaban, I. E. and Pyman, F. L., Journ. Chem. Soc. London, 1922, Trans. vol. 121, p. 954 Google Scholar.

Page 400 note 1 Light, L. and Pyman, F. L., Journ. Chem. Soc. London, 1922, Trans. vol. 121, p. 2629.CrossRefGoogle Scholar

Page 401 note 1 Balaban, I. E. and Pyman, F. L., Journ. Chem. Soc. London, Trans. vol. 125, p. 1568.Google Scholar

Page 402 note 1 Michaelis, A. and Soden, H. v., Ann. Chem. (Liebig) 1885, vol. 229, p. 306.CrossRefGoogle Scholar

Page 403 note 1 Walker, T. K., Journ. Inst. Brewing, 1924, vol. 30, p. 721.Google Scholar

Page 404 note 1 Robinson, R. and Thornley, S., Jour. Chem. Soc. London, 1924, Trans. vol. 125, p. 2169.CrossRefGoogle Scholar