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Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data

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Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data. / Chan, FC; Anwar, J; Cernik, R et al.
In: Journal of Applied Crystallography, Vol. 32, 01.06.1999, p. 436-441.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Chan, FC, Anwar, J, Cernik, R, Barnes, P & Wilson, RM 1999, 'Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data', Journal of Applied Crystallography, vol. 32, pp. 436-441. https://doi.org/10.1107/S0021889898017233

APA

Chan, FC., Anwar, J., Cernik, R., Barnes, P., & Wilson, RM. (1999). Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data. Journal of Applied Crystallography, 32, 436-441. https://doi.org/10.1107/S0021889898017233

Vancouver

Chan FC, Anwar J, Cernik R, Barnes P, Wilson RM. Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data. Journal of Applied Crystallography. 1999 Jun 1;32:436-441. doi: 10.1107/S0021889898017233

Author

Chan, FC ; Anwar, J ; Cernik, R et al. / Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data. In: Journal of Applied Crystallography. 1999 ; Vol. 32. pp. 436-441.

Bibtex

@article{3bf28895b178468caeb910624d3c78b3,
title = "Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data",
abstract = "The crystal structure of sulfathiazole [4-amino-N-(2,3-dihydro-2-thiazolylidene)benzenesulfonamide, C9H9-N3O2S] polymorphic form V has been determined from high-resolution synchrotron X-ray powder diffraction data. The structure is monoclinic, space group P2(1)/in, Z = 8, with two molecules in the asymmetric unit. The unit-cell dimensions are a = 14.3296(3), b = 15.2733 (2), c = 10.4428 (2) Angstrom and beta = 91.052 (1)degrees with cell volume V = 2285.13 (8) Angstrom(3). The structure has been solved by direct methods without recourse to any computational modelling techniques for generating possible structures. The unrefined structure obtained from direct methods gave an R-wp value of 36.5%. Refinement of atomic and displacement parameters yielded a final R-wp of 12.54% (R-p = 9.37%). The conformations of the two molecules in the asymmetric unit are nearly identical and very similar to that found in other forms of sulfathiazole. The molecular packing is characterized by molecular sheets lying perpendicular to the a axis. Each sheet is two molecules thick, being integrated by hydrogen bonding. With 16 non-H atoms in the molecule and two molecules in the asymmetric unit, this structure represents a further advance in terms of the complexity of an organic structure solved from X-ray powder diffraction data.",
keywords = "CRYSTAL, DIFFRACTOMETRY, PREFERRED-ORIENTATION",
author = "FC Chan and J Anwar and R Cernik and P Barnes and RM Wilson",
year = "1999",
month = jun,
day = "1",
doi = "10.1107/S0021889898017233",
language = "English",
volume = "32",
pages = "436--441",
journal = "Journal of Applied Crystallography",
issn = "0021-8898",
publisher = "Wiley Blackwell",

}

RIS

TY - JOUR

T1 - Ab initio structure determination of sulfathiazole polymorph V from synchrotron X-ray powder diffraction data

AU - Chan, FC

AU - Anwar, J

AU - Cernik, R

AU - Barnes, P

AU - Wilson, RM

PY - 1999/6/1

Y1 - 1999/6/1

N2 - The crystal structure of sulfathiazole [4-amino-N-(2,3-dihydro-2-thiazolylidene)benzenesulfonamide, C9H9-N3O2S] polymorphic form V has been determined from high-resolution synchrotron X-ray powder diffraction data. The structure is monoclinic, space group P2(1)/in, Z = 8, with two molecules in the asymmetric unit. The unit-cell dimensions are a = 14.3296(3), b = 15.2733 (2), c = 10.4428 (2) Angstrom and beta = 91.052 (1)degrees with cell volume V = 2285.13 (8) Angstrom(3). The structure has been solved by direct methods without recourse to any computational modelling techniques for generating possible structures. The unrefined structure obtained from direct methods gave an R-wp value of 36.5%. Refinement of atomic and displacement parameters yielded a final R-wp of 12.54% (R-p = 9.37%). The conformations of the two molecules in the asymmetric unit are nearly identical and very similar to that found in other forms of sulfathiazole. The molecular packing is characterized by molecular sheets lying perpendicular to the a axis. Each sheet is two molecules thick, being integrated by hydrogen bonding. With 16 non-H atoms in the molecule and two molecules in the asymmetric unit, this structure represents a further advance in terms of the complexity of an organic structure solved from X-ray powder diffraction data.

AB - The crystal structure of sulfathiazole [4-amino-N-(2,3-dihydro-2-thiazolylidene)benzenesulfonamide, C9H9-N3O2S] polymorphic form V has been determined from high-resolution synchrotron X-ray powder diffraction data. The structure is monoclinic, space group P2(1)/in, Z = 8, with two molecules in the asymmetric unit. The unit-cell dimensions are a = 14.3296(3), b = 15.2733 (2), c = 10.4428 (2) Angstrom and beta = 91.052 (1)degrees with cell volume V = 2285.13 (8) Angstrom(3). The structure has been solved by direct methods without recourse to any computational modelling techniques for generating possible structures. The unrefined structure obtained from direct methods gave an R-wp value of 36.5%. Refinement of atomic and displacement parameters yielded a final R-wp of 12.54% (R-p = 9.37%). The conformations of the two molecules in the asymmetric unit are nearly identical and very similar to that found in other forms of sulfathiazole. The molecular packing is characterized by molecular sheets lying perpendicular to the a axis. Each sheet is two molecules thick, being integrated by hydrogen bonding. With 16 non-H atoms in the molecule and two molecules in the asymmetric unit, this structure represents a further advance in terms of the complexity of an organic structure solved from X-ray powder diffraction data.

KW - CRYSTAL

KW - DIFFRACTOMETRY

KW - PREFERRED-ORIENTATION

U2 - 10.1107/S0021889898017233

DO - 10.1107/S0021889898017233

M3 - Journal article

VL - 32

SP - 436

EP - 441

JO - Journal of Applied Crystallography

JF - Journal of Applied Crystallography

SN - 0021-8898

ER -