The crystallization behavior of (±)-cis-α-[Co(dmtrien)(NO2)2]Cl· 0.5H2O 1 and (±)-cis-α-[Co(dmtrien)(NO2)2]I 2[hair space]† (dmtrien = 3,6-dimethyl-3,6-diazaoctane-1,8-diamine)

(Note: The full text of this document is currently only available in the PDF Version )

Jiwen Cai, Jozef Myrczek, Hyungphil Chun and Ivan Bernal


Abstract

The compound (±)-cis-α-[Co(dmtrien)(NO2)2]Cl·0.5H2O 1 has been found to crystallize as a kryptoracemate in the space group C2 (Z = 4) with a racemic pair as the asymmetric unit, whereas (±)-cis-α-[Co(dmtrien)(NO2)2]I 2 crystallizes as a simple racemate, as expected (dmtrien = 3,6-dimethyl-3,6-diazaoctane-1,8-diamine). For 1 the two cations in the asymmetric unit had the conformations Δ(λδλ), Co(1), and Λ(δλδ), Co(2), and those of the chiral, methylated, nitrogens of Co(1) are (S,S) while those of Co(2) are (R,R). Compound 2 crystallizes as a racemate in the space group Pccn (Z = 8); the anions are in a general position but there are two half cations sitting at two-fold axes of the space group. For 1, Co(1) and Co(2) cations form separate spiral strings which extend through the length of the a axis, and these strings are held together by hydrogen bonds to the anions and waters of crystallization. Each string contains, exclusively, cations of single chirality and layers of homochiral strings define the ab plane of the crystals. Each layer is of opposite chirality to the pair of adjacent ones. In 2 the packing is different in that there are strings made exclusively of either Co(1) or Co(2) running along the diagonal of the bc plane, as well as [–Co(1)–Co(2)–Co(1)–Co(2)–]n . . . strings running parallel to the c axis.


References

  1. For the preceding parts, see I. Bernal, J. Cai and J. Myrczek, Acta Chim. Hung. Models in Chemistry, 1995, 132, 451 Search PubMed.
  2. I. Bernal, J. Cai, S. S. Massoud, S. F. Watkins and F. Fronczek, J. Coord. Chem., 1996, 38, 165 CAS.
  3. (a) K. Yamasaki, H. Igarashi, Y. Yoshikawa and H. Kuroya, Inorg. Nucl. Chem. Lett., 1968, 4, 491 Search PubMed and refs. therein; (b) A. Fuyuhiro, K. Yamanari and Y. Shimura, Bull. Chem. Soc. Jpn., 1981, 54, 2531 CAS.
  4. I. Bernal, F. Somoza and V. Banh, J. Coord. Chem., 1997, 42, 1 CAS.
  5. M.-C. Rodriguez, M. Cesario, J. J. Guilhem, B. Keita and L. Nadjo, Inorg. Chem., 1996, 35, 7804 CrossRef CAS.
  6. H. J. Haupt and F. Huber, Z. Anorg. Allg. Chem., 1978, 442, 31 CAS.
  7. (a) I. Bernal, Inorg. Chim Acta, 1985, 96, 99 CrossRef CAS; (b) I. Bernal and J. Cetrullo, Inorg. Chim. Acta, 1987, 134, 105 CrossRef CAS.
  8. TEXRAY-230, a modification of the SDP-Plus set of X-ray crystallographic programs, for use with the CAD-4 diffractometer, Molecular Structure Corporation, Woodlands, TX, 1985.
  9. SDP-Plus, Enraf-Nonius Corporation X-ray diffraction data processing program, distributed by B. A. Frenz & Associates, College Station, TX, 1982.
  10. R. B. Roof, A Theoretical Extension of the Reduced Cell Concept in Crystallography, Report LA-4038, Los Alamos Scientific Laboratory, 1969 Search PubMed.
  11. G. M. Sheldrick, Acta Crystallogr., Sect. A, 1990, 46, 467 CrossRef.
  12. G. M. Sheldrick, SHELXL 93, University of Göttingen, 1993.
  13. I. Bernal, J. Cetrullo and J. Myrczek, Mater. Chem. Phys., 1993, 35, 290 CAS.
  14. I. Bernal, J. Myrczek and J. Cai, Polyhedron, 1993, 12, 1149 CrossRef CAS.
  15. I. Bernal, J. Cetrullo and S. Berhane, Struct. Chem., 1990, 1, 361 CAS.
  16. I. Bernal, J. Cetrullo, J. H. Worrell and T. Li, Polyhedron, 1994, 13, 463 CrossRef CAS.
  17. I. Bernal, J. Cetrullo, J. Cai, R. A. Geanangel and J. H. Worrell, J. Chem. Soc., Dalton Trans., 1995, 99 RSC.
  18. H. Flack, Acta Crystallogr., Sect. A, 1983, 39, 876 CrossRef.
  19. A. C. Larson, F. L. Lee, Y. Le Page, M. Webster, J. P. Charland and E. J. Gabe, The NRCVAX Crystal Structure System, as adapted for PC use by Peter S. White, University of North Carolina, Chapel Hill, NC, 1992.
  20. O. Bortin, Acta Chem. Scand., Ser. A, 1976, 30, 657.
  21. P. J. Toscano, K. J. Fordon, L. M. Engelhardt, B. W. Skelton, A. H. White and P. A. Marzilli, Polyhedron, 1990, 2, 323.
  22. V. G. Albano, P. Bellon and M. Sansoni, J. Chem. Soc. D, 1969, 899 RSC; V. G. Albano, G. M. Ricci and M. Sansoni, Inorg. Chem., 1969, 8, 2109 CrossRef CAS; V. G. Albano, P. Bellon and M. Sansoni, J. Chem. Soc. A, 1971, 2420 RSC.
  23. A. I. Kitaigorodskii, Mixed Crystals, Springer, Berlin, 1984. The packing of optically active substances is dealt with in considerable detail in ch. 12, particularly in section 12.7, pp. 248–251 Search PubMed.
  24. J. Jacques, A. Collet and S. H. Wilen, Enantiomers, Racemates and Resolutions, Wiley-Interscience, New York, 1981 Search PubMed.
Click here to see how this site uses Cookies. View our privacy policy here.