Kinetics and Mechanism of the Complexation of trans-Diamminediaquaplatinum(II) with the 6-Oxopurine Nucleosides Inosine and 1-Methylinosine in Aqueous Solution as a Function of the pH

Inorganic Chemistry

Volumn 35, Issue 26, 1996, Pages 7556-7562

  Mikola, Marjaana ^a   Arpalahti, Jorma ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0007751064     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic960828f     Document Type: Article

References (43)

1. (a) Lippert, B. In Progress in Inorganic Chemistry; Lippard, S. J., Ed.; Wiley: New York, 1989; Vol. 37, pp 1-97.
2. (b) Sundqvist, W. I.; Lippard, S. J. Coord. Chem. Rev. 1990, 100, 293-322.
3. (c) Bruhn, S. L.; Toney, J. H.; Lippard, S. J. In Progress in Inorganic Chemistry; Lippard, S. J., Ed.; Wiley: New York, 1990; Vol. 38, pp 477-516.
4. (d) Reedijk, J. J. Chem. Soc., Chem Commun. 1996, 801-806.
5. (a) Arpalahti, J. In Metal ions in Biological Systems; Sigel, H., Sigel, A., Eds.; Marcel Dekker: New York, 1996; Vol. 32, pp 379-395.
6. (b) Farrell, N. In Metal Ions in Biological Systems; Sigel, H., Sigel, A., Eds.; Marcel Dekker: New York. 1996; Vol. 32, pp 603-639. See also other chapters in this volume.
7. Arpalahti, J.; Mikola, M.; Mauristo, S. Inorg. Chem. 1993, 32, 3327- 3332.
8. Mikola, M.; Arpalahti, J. Inorg. Chem. 1994, 32, 4439-4445.
9. Arpalahti, J. Inorg. Chem. 1990, 29, 4598-4602.
10. (a) Arpalahti, J.; Lippert, B. Inorg. Chem. 1990, 29, 104-110.
11. (b) Eapen, S.; Green, M.; Ismail, I. M. J. Inorg. Biochem. 1985, 24, 233- 237.
12. (a) Evans, D. J.; Ford, N. R.; Green, M. Inorg. Chim. Acta 1986, 125, L39-L40.
13. (b) Evans, D. J.; Green, M.; van Eldik, R. Inorg. Chim. Acta 1987, 128, 27-29.
14. (a) Laoui, A.; Kozelka, J.; Chottard, J.-C. Inorg. Chem. 1988, 27, 2751-2753.
15. (b) Gonnet, F.; Reeder, F.; Kozelka, J.; Chottard, J.-C. Inorg. Chem. 1996, 35, 1653-1658.
16. (a) Johnson, N. P.; Hoeschele, J. D.; Rahn, R. O. Chem.-Biol. Interact. 1980, 30, 151-169.
17. (b) Schaller, W.; Reisner, H.; Holler, E. Biochemistry 1987, 26, 943-950.
18. Appleton, T. G.; Bailey, A. J.; Barnham, K. J.; Hall, J. R. Inorg. Chem. 1992, 31, 3077-3082.
19. Arpalahti, J.; Sillanpää, R.; Barnham, K. J.; Sadler, P. J. Acta Chem. Scand. 1996, 50, 181-184.
20. (a) Ciccarelli, R. B.; Solomon, M. J.; Varshavsky, A.; Lippard, S. J. Biochemistry 1985, 24, 7533-7540.
21. (b) Heiger-Bernays, W. J.; Essigmann, J. M.; Lippard, S. J. Biochemistry 1990, 29, 8461-8466.
22. (a) van der Veer, J. L.; Ligtvoet, G. J.; van den Elst, H.; Reedijk, J. J. Am. Chem. Soc. 1986, 108, 3860-3862.
23. (b) Gibson, D.; Lippard, S. J. Inorg. Chem. 1987, 26, 2275-2279.
24. (c) Lepre, C. A.; Chassot, L.; Costello, C. E.; Lippard, S. J. Biochemistry 1990, 29, 811-823.
25. Basolo, F.; Pearson, R. G., Mechanism of Inorganic Reactions; Wiley: New York, 1967, Chapter 5.
26. Abbreviations: acetic acid (HAc), inosine (InoH), 1-methylinosine (MeIno), 4-morpholineethanesulfonic acid (MES) and -propanesulfonic acid (MOPS), triethanolamine (TEA).
27. Mikola, M.; Oksman, P.; Arpalahti, J. J. Chem. Soc., Dalton Trans. 1996, 3101-3104.
28. Good, N. E.; Winget, G. D.; Winter, W.; Connolly, T. N.; Izawa, S.; Singh, R. M. M. Biochemistry 1966, 5, 467-477.
29. Good, N. E.; Izawa, S. Methods Enzymol. Part B 1972, 24, 53-68.
30. Appleton, T. G.; Berry, R. D.; Davis, C. A.; Hall, J. R.; Kimlin, H. A. Inorg. Chem. 1984, 23, 3514-3521.
31. Arpalahti, J.; Lehikoinen, P. Inorg. Chem. 1990, 29, 2564-2567.
32. T < 0.1 mM.
33. Lönnberg, H.; Vihanto, P. Inorg. Chim. Acta 1981, 56, 157-161.
34. -(7.3±0.1) M.
35. Mean values of three independent measurements.
36. Jensen, K. A. Z Anorg. Allgem. Chem. 1939, 242, 87-91. See also ref 10.
37. Martin, R. B. Acc. Chem. Res. 1985, 18, 32-38.
38. -1.
39. For example, see: (a) Raudaschl-Sieber, G.; Schöllhorn, H.; Thewalt, U.; Lippert, B. J. Am. Chem. Soc. 1985, 107, 3591-3595. (b) Miller, S. K.; Marzilli, L. G. Inorg. Chem. 1985, 24, 2421-2425. van der Veer, J. L.; van den Elst, H.; Reedijk, J. Inorg. Chem. 1987, 26, 1536- 1540.
40. For example, see: (a) Raudaschl-Sieber, G.; Schöllhorn, H.; Thewalt, U.; Lippert, B. J. Am. Chem. Soc. 1985, 107, 3591-3595. (b) Miller, S. K.; Marzilli, L. G. Inorg. Chem. 1985, 24, 2421-2425. van der Veer, J. L.; van den Elst, H.; Reedijk, J. Inorg. Chem. 1987, 26, 1536- 1540.
41. For example, see: (a) Raudaschl-Sieber, G.; Schöllhorn, H.; Thewalt, U.; Lippert, B. J. Am. Chem. Soc. 1985, 107, 3591-3595. (b) Miller, S. K.; Marzilli, L. G. Inorg. Chem. 1985, 24, 2421-2425. van der Veer, J. L.; van den Elst, H.; Reedijk, J. Inorg. Chem. 1987, 26, 1536- 1540.
42. Schröder, G.; Lippert, B.; Sabat, M.; Lock, C. J. L.; Faggiani, R.; Song, B.; Sigel. H. J. Chem. Soc., Dalton Trans. 1995, 3767-3775.
43. d,obs. Peak areas of 1b, rather than concentrations, were used in computations.