Can a small amount of crystal solvent be overlooked or have no structural effect? Isomorphous non-stoichiometric hydrates (pseudo-polymorphs): The case of salicylaldehyde thiosemicarbazone

CrystEngComm

Volumn 12, Issue 11, 2010, Pages 3526-3530

  Monfared, Hassan Hosseini ^a   Chamayou, Anne Christine ^b   Khajeh, Soliman ^a   Janiak, Christoph ^b  

^a UNIVERSITY OF ZANJAN   (Iran)

^b UNIVERSITY OF FREIBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77958131186     PISSN: 14668033     EISSN: 14668033     Source Type: Journal    
DOI: 10.1039/c0ce00041h     Document Type: Article

References (73)

1. C. Aakeröy N. R. Champness C. Janiak CrystEngComm 2010 12 22 43
2. F. H. Herbstein Cryst. Growth Des. 2004 4 1419 1429
3. Recent work on polymorphs: C. Janiak A.-C. Chamayou A. K. M. R. Uddin M. Uddin K. S. Hagen M. Enamullah Dalton Trans. 2009 3698 3709
4. R. Cong J. Zhu Y. Wang T. Yang F. Liao C. Jin J. Lin CrystEngComm 2009 11 1971 1978
5. Y. Fan W. Song D. Yu K. Ye J. Zhang Y. Wang CrystEngComm 2009 11 1716 1722
6. K. Manoj R. G. Gonnade M. M. Bhadbhade M. S. Shashidhar CrystEngComm 2009 11 1022 1029
7. M. Kitamura CrystEngComm 2009 11 949 964
8. W. Zhang X. Tang H. Ma W.-H. Sun C. Janiak Eur. J. Inorg. Chem. 2008 2830 2836
9. T. Gelbrich D. S. Hughes M. B. Hursthouse T. L. Threlfall CrystEngComm 2008 10 1328 1334
10. A. Brillante I. Bilotti R. G. Della Valle E. Venuti A. Girlando CrystEngComm 2008 10 937 946
11. J. S. Field L. P. Ledwaba O. Q. Munro D. R. McMillin CrystEngComm 2008 10 740 747
12. I. Barsky J. Bernstein CrystEngComm 2008 10 669 674
13. S. Janbon R. J. Davey K. Shankland CrystEngComm 2008 10 279 282
14. P. Munshi B. W. Skelton J. J. McKinnon M. A. Spackman CrystEngComm 2008 10 197 206
15. Recent experimental and theoretical work on polymorphs: M. A. Neumann M.-A. Perrin CrystEngComm 2009 11 2475 2479
16. S. Mohamed S. A. Barnett D. A. Tocher S. L. Price K. Shankland C. K. Leech CrystEngComm 2008 10 399 404
17. T. C. Lewis D. A. Tocher G. M. Day S. L. Price CrystEngComm 2003 5 3 9
18. A. T. Anghel G. M. Day S. L. Price CrystEngComm 2002 4 348 355
19. M. A. Spackman J. J. McKinnon CrystEngComm 2002 4 378 392
20. J. J. McKinnon F. P. A. Fabbiani M. A. Spackman Cryst. Growth Des. 2007 7 755 769
21. K. R. Seddon Cryst. Growth Des. 2004 4 1087
22. G. R. Desiraju Cryst. Growth Des. 2004 4 1089 1090
23. J. Ruiz V. Rodriguez N. Cutillas A. Hoffmann A.-C. Chamayou K. Kazmierczak C. Janiak CrystEngComm 2008 10 1928 1938
24. Recent work on solvates (pseudo-polymorphs): V. T. Nguyen R. Bishop D. C. Craig M. L. Scudder CrystEngComm 2009 11 1275 1280
25. D. Kovala-Demertzi J. Wiecek J. C. Plakatouras Z. Ciunik CrystEngComm 2008 10 1291 1295
26. R. Peng S.-R. Deng M. Li D. Li Z.-Y. Li CrystEngComm 2008 10 590 597
27. E. D. Sloan Nature 2003 426 353 363
28. Z. Huo M. D. Jager K. T. Miller E. D. Sloan, Jr. Chem. Eng. Sci. 2002 57 705 713
29. M. J. Peltre H. Pezerat J. Solid State Chem. 1978 23 19 32
30. H. Mimura S. Kitamura T. Kitagawa S. Kohda Colloids Surf., B 2002 26 397 406
31. R. K. Harris J. Pharm. Pharmacol. 2007 59 225 239
32. A. D. Gift L. S. Taylor J. Pharm. Biomed. Anal. 2007 43 14 23
33. J.-R. Authelin Int. J. Pharm. 2005 303 37 53
34. G. A. Stephenson B. A. Diseroad Int. J. Pharm. 2000 198 167 177
35. U. Griesser Acta Crystallogr., Sect. A: Found. Crystallogr. 2002 58 C241
36. P. Chakravarty R. T. Berendt E. J. Munson V. G. Young, Jr R. Govindarajan R. Suryanarayanan J. Pharm. Sci. 2010 99 1882 1895
37. P. Chakravarty R. T. Berendt E. J. Munson V. G. Young, Jr R. Govindarajan R. Suryanarayanan J. Pharm. Sci. 2010 99 816 827
38. A. C. Schmidt I. Schwarz Int. J. Pharm. 2006 320 4 13
39. J. F. Krzyzaniak G. R. Williams N. Ni J. Pharm. Sci. 2007 96 1270 1281
40. A. V. Trask W. D. S. Motherwell W. Jones Cryst. Growth Des. 2005 5 1013 1021
41. J. A. Ripmeester Supramol. Chem. 1993 2 89 91
42. M. Smrkolj A. Meden Pharmazie 2006 61 999 1004
43. J. Baronsky S. Bongaerts M. Traeubel H.-C. Weiss N. Urbanetz Eur. J. Pharm. Biopharm. 2009 71 88 99
44. S. B. Novaković B. Fraisse G. A. Bogdanović A. S. Biré Cryst. Growth Des. 2007 7 191 195
45. D. Chattopadhyay S. K. Mazumdar T. Banerjee S. Ghosh T. C. W. Mak Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 1988 44 1025 1028
46. M. C. Etter Acc. Chem. Res. 1990 23 120 126
47. M. C. Etter J. C. MacDonald J. Bernstein Acta Crystallogr., Sect. B: Struct. Sci. 1990 46 256 262
48. M. C. Etter J. Phys. Chem. 1991 95 4601 4610
49. C. Janiak J. Chem. Soc., Dalton Trans. 2000 3885 3896
50. C. Janiak A.-C. Chamayou A. K. M. R. Uddin M. Uddin K. S. Hagen M. Enamullah Dalton Trans. 2009 3698 3709
51. H. A. Habib A. Hoffmann H. A. Höppe G. Steinfeld C. Janiak Inorg. Chem. 2009 48 2166 2180
52. B. Wu X. Huang Y. Xia X.-J. Yang C. Janiak CrystEngComm 2007 9 676 685
53. B. Wisser C. Janiak Acta Crystallogr., Sect. E: Struct. Rep. Online 2007 63 o2871 o2872
54. T. Dorn C. Janiak K. Abu-Shandi CrystEngComm 2005 7 633 641
55. X.-J. Yang F. Drepper B. Wu W.-H. Sun W. Haehnel C. Janiak Dalton Trans. 2005 256 267 and supplementary material therein
56. Cambridge Structure Database (CSD), version 5.30 (November 2008) with 3 updates (February, May and September 2009).
57. PLATON recognizes disordered structures by spotting the fractional occupancies of the atoms where it then does not carry out a packing index calculation. Still, the latter may be enabled by removing one orientation of a disordered moiety and changing the occupancies of the remaining one to 1.0 in the input file, thereby trying to present PLATON with a model of the ideal crystal structure. This can sensibly be done, however, only then there are two independent disordered positions where the occupancies add up to 1.0. This is not the case in the present situation.
58. A. I. Kitaigorodskii, Molecular Crystals and Molecules, Academic Press, New York, 1973
59. A. C. Chamayou C. Biswas A. Ghosh C. Janiak Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2009 65 m311 m313
60. H. A. Habib J. Sanchiz C. Janiak Dalton Trans. 2008 1734 1744
61. Z. Duan Y. Zhang B. Zhang D. B. Zhu J. Am. Chem. Soc. 2009 131 6934 6935
62. N. Casati P. Macchi A. Sironi Chem.-Eur. J. 2009 15 4446 4457
63. A. Kondo H. Noguchi S. Ohnishi H. Kajiro A. Tohdoh Y. Hattori W.-C. Xu H. Tanaka H. Kanoh K. Kaneko Nano Lett. 2006 6 2581
64. D. Armentano G. De Munno T. F. Mastropietro M. Julve F. Lloret J. Am. Chem. Soc. 2005 127 10778
65. A. K. Sah T. Tanase Chem. Commun. 2005 5980
66. J.-P. Ma Y.-B. Dong R.-Q. Huang M. D. Smith C.-Y. Su Inorg. Chem. 2005 44 6143
67. M.-H. Zeng X.-L. Feng X.-M. Chen Dalton Trans. 2004 2217
68. R. Kuroda K. Higashiguchi S. Hasebe Y. Imai CrystEngComm 2004 6 463 468
69. C. Hu U. Englert Angew. Chem., Int. Ed. 2005 44 2281
70. SMART, Data Collection Program for the CCD Area-Detector System; SAINT, Data Reduction and Frame Integration Program for the CCD Area-Detector System. Bruker Analytical X-ray Systems, Madison, Wisconsin, USA, 1997-2006
71. G. Sheldrick, Program SADABS: Area-Detector Absorption Correction, University of Göttingen, Germany, 1996
72. G. M. Sheldrick Acta Crystallogr., Sect. A: Found. Crystallogr. 2008 64 112 122
73. K. Brandenburg, Diamond (version 3.2d), Crystal and Molecular Structure Visualization, Crystal Impact, K. Brandenburg & H. Putz Gbr, Bonn (Germany), 2009