Synthesis and solution studies of ruthenium(II) complexes with thiazole and antileukaemic drug thiopurines. Crystal structure of trans-dichlorotris(1,3-thiazole)(triphenylphosphine)ruthenium(II)[hair space]

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

Claudia Pifferi and Renzo Cini


Abstract

The crystalline complexes [RuCl2(PPh3)2(thz)2] 1, [RuCl2(PPh3)(thz)3] 2, [Ru(H2tp)2(PPh3)(thz)]Cl2·2H2O 3·2H2O, [Ru(H2tg)2(PPh3)2]Cl2·2H2O·EtOH 4·2H2O·EtOH, [Ru(H2tprta)2(PPh3)2]Cl2·3H2O 5·3H2O, [Ru(H2tp)2(PPh3)2][CF3SO3]2·H2O·EtOH 6·H2O·EtOH, [Ru(H2tg)2(PPh3)2][CF3SO3]2·3H2O 7·3H2O, [Ru(H2tp)2(AsPh3)(MeOH)]Cl2·MeOH 8·MeOH, [Ru(bzim)2Cl2(PPh3)2] 9, and [RuCl2(PPh3)2(mpym)2] 10 (H2tg = purine-2-amino-6-thione, H2tp = purine-6-thione, H2tprta = purine-6-thione 2′,3′,5′-tri-O-acetylriboside, thz = 1,3-thiazole, bzim = benzimidazole, mpym = 4-methylpyrimidine) have been prepared from [RuCl2(PPh3)3] or [RuCl3(AsPh3)2(MeOH)] and the base in alcoholic solution under nitrogen. The structures of the complexes were investigated by X-ray diffraction (2), NMR, conventional spectroscopic techniques and electrochemical methods. All the complex molecules have a pseudo-octahedral co-ordination geometry. The donor set of 2 consists of a phosphorus atom, two chloride anions trans to each other and three thz ligands bound to the metal through nitrogen. The sulfur atom of thz does not show any donor ability. However, the thione function of purine is much more active and in complexes 3–8 the purine base is chelated through S and N(7) atoms. On refluxing a suspension of 2 and H2tp in ethanol compound 3 was obtained, which has a slight solubility in water. Electrochemical studies carried out on 7 in acetonitrile revealed a monoelectronic oxidation process at E½ 1.02 V. The [RuIII(H2tg)2(PPh3)2]3+ species which forms at this potential is relatively stable under the experimental conditions [25 °C; N2, 1 bar (105 Pa)] can be reversibly reduced to the starting compound which was recovered from the mixture. A molecular mechanics analysis, carried out for 1 and 2, produced a force field for this class of compounds and showed that the trans,trans,trans-[RuCl2(PPh3)2(thz)2] isomer of 1 is the most stable.


References

  1. (a) J. Reedijk, J. Chem. Soc., Dalton Trans., 1996, 801 RSC; (b) Y. Chen, F.-T. Lin and R. E. Shepherd, Inorg. Chem., 1997, 36, 818 CrossRef CAS; (c) M. Hartmann, T. J. Einhäuser and B. K. Keppler, Chem. Commun., 1996, 1741 RSC; (d) L. M. Torres and L. G. Marzilli, J. Am. Chem. Soc., 1991, 113, 4678 CrossRef CAS; (e) S. Mukundan, jun., Y. Xu, G. Zon and L. G. Marzilli, J. Am. Chem. Soc., 1991, 113, 3021 CrossRef; (f) M. Krumm, I. Mutikainen and B. Lippert, Inorg. Chem., 1991, 30, 890; (g) L. G. Marzilli, New J. Chem., 1990, 14, 409 Search PubMed and refs. therein; (h) E. L. M. Lempers and J. Reedijk, Inorg. Chem., 1990, 29, 1880 CrossRef CAS; (i) M. J. Bloemink, E. L. M. Lempers and J. Reedijk, Inorg. Chim. Acta, 1990, 76, 317 CrossRef CAS; (j) S. E. Sherman and S. Lippard, Chem. Rev., 1987, 87, 1153 CrossRef CAS and refs. therein; (k) P. Köpf-Maier and H. Köpf, Chem. Rev., 1987, 87, 1137 CrossRef and refs. therein; (l) B. Lippert, Prog. Inorg. Chem., 1989, 37, 1 CAS and refs. therein; (m) E. Alessio, Y. Xu, S. Cauci, G. Mestroni, F. Quadrifoglio, P. Viglino and L. G. Marzilli, J. Am. Chem. Soc., 1989, 111, 7068 CrossRef CAS; (n) H. R. Rubin, T. P. Haromy and M. Sundaralingam, Acta Crystallogr., Sect. C, 1991, 47, 1712 CrossRef; (o) K. Aoki, M. Moshino, T. Okada, H. Yamazaki and H. Sekizawa, J. Chem. Soc., Chem. Commun., 1986, 314 RSC; (p) D. W. Abbott and C. Woods, Inorg. Chem., 1983, 22, 597 CrossRef CAS; (q) R. J. Broomfield, R. H. Dainty, R. D. Gillard and B. J. Heaton, Nature (London), 1969, 223, 735; (r) B. Rosenberg, in Metal Ions in Biology, ed. T. G. Spiro, Wiley, New York, 1980, vol. 1, ch. 1 Search PubMed.
  2. (a) C. J. Zubrod, Life Sci., 1974, 14, 809 CrossRef CAS; (b) D. R. Williams, Chem. Rev., 1972, 72, 203 CrossRef CAS; (c) H. B. Wood, jun., Cancer Chemother. Rep., Part 3, 1971, 2, 9 Search PubMed; (d) Comprehensive Medicinal Chemistry, eds. C. Hansch, P. G. Sammes, J. B. Taylor, J. C. Emmett, P. D. Kennewell and C. A. Ramsden, Pergamon, Oxford, 1990 Search PubMed.
  3. C. M. Dupureur and J. K. Barton, Inorg. Chem., 1997, 36, 33 CrossRef CAS; M. R. Arkin, E. D. A. Stemp, R. E. Holmlin, J. K. Barton, A. Hormann, E. J. C. Olson and P. F. Barbara, Science, 1996, 273, 475 CrossRef CAS; A. M. Pyle and J. K. Barton, Prog. Inorg. Chem., Bioinorg. Chem., 1990, 38, 413 Search PubMed.
  4. (a) R. Cini, R. Bozzi, A. Karaulov, M. B. Hursthouse, A. Calafat and L. G. Marzilli, J. Chem. Soc., Chem. Commun., 1993, 899 RSC; (b) R. Cini, A. Cinquantini, M. Sabat and L. G. Marzilli, Inorg. Chem., 1985, 24, 3903 CrossRef CAS.
  5. A. Cavaglioni and R. Cini, J. Chem. Soc., Dalton Trans., 1997, 1149 RSC; Polyhedron, 1997, 16, 4045 Search PubMed.
  6. P. J. Brothers, Prog. Inorg. Chem., 1981, 28, 1 CAS; D. E. Fogg, B. R. James and M. Kilner, Inorg. Chim. Acta, 1994, 222, 85 CrossRef CAS.
  7. A. Cinquantini, R. Cini, R. Seeber and P. Zanello, J. Electroanal. Chem., 1980, 111, 309 CrossRef CAS.
  8. T. A. Stephenson and G. Wilkinson, J. Inorg. Nucl. Chem., 1966, 28, 945 CrossRef CAS.
  9. G. M. Sheldrick, SHELXS 86, Program for Crystal Structure Determination, University of Göttingen, 1986.
  10. G. M. Sheldrick, SHELXL 93, Program for Crystal Structure Refinement, University of Göttingen, 1993.
  11. M. Nardelli, PARST 95, A System of Computer Routines for Calculating Molecular Parameters from Results of Crystal Structure Analysis, University of Parma, 1995.
  12. F. Mohamadi, N. G. J. Richars, W. C. Guida, R. Liskamp, M. Lipton, C. Caufield, G. Chang, T. Hendrickson and W. C. Still, J. Comput. Chem., 1990, 11, 440 CrossRef CAS.
  13. W. D. Cornell, P. Cieplak, C. I. Bayly, I. R. Gould, K. M. jun. Merz, D. M. Ferguson, D. C. Spellmeyer, T. Fox, J. W. Caldwell and P. A. Kollman, J. Am. Chem. Soc., 1995, 117, 5179 CrossRef CAS.
  14. R. M. Badger, J. Chem. Phys., 1934, 2, 128 CrossRef CAS.
  15. R. M. Badger, J. Chem. Phys., 1935, 3, 710 CAS.
  16. D. R. Hershbach and V. W. Laurie, J. Chem. Phys., 1961, 35, 458 CrossRef CAS.
  17. A. Halgren, J. Mol. Struct. (THEOCHEM), 1988, 163, 431 CrossRef.
  18. A. Halgren, J. Am. Chem. Soc., 1990, 112, 4710 CrossRef CAS.
  19. S. Geremia and M. Calligaris, J. Chem. Soc., Dalton Trans., 1997, 1541 RSC.
  20. (a) GAUSSIAN 92/DFT, Revision F.2, M. J. Frisch, G. W. Trucks, H. B. Schlegel, P. M. W. Gill, B. G. Johnson, M. W. Wong, J. B. Foresman, M. A. Robb, M. Head-Gordon, E. S. Reploge, R. Gomperts, J. L. Andres, K. Raghavachari, J. S. Binkley, C. Gonzales, R. L. Martin, D. J. Fox, D. J. Defrees, J. Baker, J. J. P. Stewart and J. A. Pople, Gaussian, Inc., Pittsburgh PA, 1993; (b) A. D. Becke, J. Chem. Phys., 1988, 88, 1053 CrossRef CAS; (c) C. Lee, W. Yang and R. G. Parr, Phys. Rev. B, 1988, 37, 785 CrossRef CAS.
  21. L. Zsolani, XPMA and ZORTEP, Interactive ORTEP Programs, University of Heidelberg, 1994.
  22. S. J. La Placa and J. A. Ibers, Inorg. Chem., 1965, 4, 778 CrossRef CAS.
  23. M. Henn, E. Alessio, G. Mestroni, M. Calligaris and W. M. Attia, Inorg. Chim. Acta, 1991, 187, 39 CrossRef CAS.
  24. L. Barloy, S. Y. Ku, J. A. Osborn, A. De Cian and J. Fischer, Polyhedron, 1996, 16, 291 CrossRef.
  25. W. S. Sheldrick and R. Exner, Inorg. Chim. Acta, 1992, 195, 1 CrossRef CAS.
  26. (a) P. Mura, B. G. Olby and S. D. Robinson, J. Chem. Soc., Dalton Trans., 1985, 2101 RSC; (b) P. Mura, B. G. Olby and S. D. Robinson, Inorg. Chim. Acta, 1985, 97, 45 CrossRef CAS; (c) M. F. McGuiggan and L. H. Pignolet, Inorg. Chem., 1982, 21, 2523 CrossRef CAS; (d) N. W. Alcock, A. F. Hill and M. S. Roe, J. Chem. Soc., Dalton Trans., 1990, 1737 RSC.
  27. M. Menon, A. Pramanik, N. Bag and A. Chakravorty, J. Chem. Soc., Dalton Trans., 1995, 1417 RSC.
  28. A. G. Orpen, L. Brammer, F. H. Allen, O. Kennard, D. G. Watson and R. Taylor, J. Chem. Soc., Dalton Trans., 1989, S1 RSC.
  29. M. M. Muir, M. E. Cadiz and A. Balz, Inorg. Chim. Acta, 1988, 151, 209 CrossRef CAS.
  30. M. Van Beusichem and N. Farrell, Inorg. Chem., 1992, 31, 634 CrossRef CAS.
  31. (a) P. W. Armit, A. S. F. Boyd and T. A. Stephenson, J. Chem. Soc., Dalton Trans., 1975, 1663 RSC; (b) P. R. Hoffman and K. G. Caulton, J. Am. Chem. Soc., 1975, 97, 4221 CrossRef CAS.
  32. N. Kottmair and W. Beck, Inorg. Chim. Acta, 1979, 34, 137 CrossRef CAS.
  33. L. J. Bellamy, The Infrared Spectra of Complex Molecules, Chapman and Hall, London, 1975, vol. 1 Search PubMed.
  34. A. Grigoratou and N. Katsaros, Inorg. Chim. Acta, 1985, 108, 41 CrossRef.
  35. R. Barbieri, E. Rivarola and F. Di Bianca, Inorg. Chim. Acta, 1985, 25, 131.
  36. N. Katsaros and A. Grigoratou, J. Inorg. Biochem., 1985, 25, 131 CrossRef CAS.
  37. M. Gleria, F. Minto, G. Beggiato and P. Bortolus, J. Chem. Soc., Chem. Commun., 1978, 285 Search PubMed.
  38. G. Altona and M. Sundaralingam, J. Am. Chem. Soc., 1973, 95, 2333 CrossRef CAS.
Click here to see how this site uses Cookies. View our privacy policy here.