Electron Transfer Reactions of RuIII(edta) Containing the N-Heterocyclic Ligand Pyrazine: Kinetic and Mechanistic Studies

Debabrata Chatterjee^a,b@ and Rudi van Eldik^b,c,d

^aVice-Chancellor’s Research Group, Zoology Department, University of Burdwan, 713104 Burdwan, India

^bDepartment of Chemistry and Pharmacy, University of Erlangen-Nuremberg, 91058 Erlangen, Germany

^cFaculty of Chemistry, Jagiellonian University, 30-387 Krakow, Poland

^dFaculty of Chemistry, N. Copernicus University, 87-100 Torun, Poland

^@Corresponding author E-mail: dchat57@hotmail.com

DOI: 10.6060/mhc190497c
Macroheterocycles 2020 13(3) 193-200

Electron transfer reactions involving Ru(III) complexes pioneered by Nobel Laureate Henry Taube in the ‘late sixties’, has been an area of continued research for more than the past five decades. This review focuses on the research progress in the use of a Ru(III) complex containing the ‘edta’ ligand (edta^4– = ethylenediaminetetraacetate) in electron transfer processes, and mainly covers the electron transfer reaction of [Ru^III(edta)(pz)]^– (pz = pyrazine) with biologically important reductants, viz. L-ascorbic acid, catechol, sulfite, sulfide and thiols, highlighting the authors’ own research work. The scope of this review is to contribute to the mechanistic understanding of electron transfer reactions of [Ru^III(edta)(pz)]^– with aforementioned biologically important electron donors, and to illustrate the preferential reaction pathway(s).

References:

Click here to expand or collapse this section

1. Chatterjee D. Coord. Chem. Rev. 1998, 168, 273.
https://doi.org/10.1016/S0010-8545(97)00072-6

2. Chatterjee D., Mitra A. De G.S. Platinum Met. Rev. 2006, 50, 2.
https://doi.org/10.1595/147106705X82874

3. Chatterjee D., van Eldik R. Adv. Inorg. Chem. 2012, 64, 183.
https://doi.org/10.1016/B978-0-12-396462-5.00006-4

4. Chatterjee D., van Eldik R. Coord. Chem. Rev. 2017, 349, 129.
https://doi.org/10.1016/j.ccr.2017.08.024

5. Matsubara T., Creutz C. Inorg. Chem. 1979, 18, 1956.
https://doi.org/10.1021/ic50197a047

6. Bajaj H.C., van Eldik R. Inorg. Chem. 1988, 27, 4052.
https://doi.org/10.1021/ic00295a031

7. Taqui Khan M.M., Bajaj H.C., Shirin Z., Venkatasubraminan K. Ind. J. Chem. (A) 1992, 31, 303.

8. Taqui Khan M.M., Chatterjee D., Merchant R.R., Paul P., Abdi S.H.R., Siddiqui M.R.H., Srinivas D., Moiz M.A., Bhadbhade M.M., Venkatasubraminan K. Inorg. Chem. 1992, 31, 2711.
https://doi.org/10.1021/ic00039a010

9. Chatterjee D. J. Chem. Soc. Dalton Trans. 1996, 4389.
https://doi.org/10.1039/DT9960004389

10. Meyer T.J., Taube H. Inorg. Chem. 1968, 7, 2369.
https://doi.org/10.1021/ic50069a038

11. Ford P.C. Coord. Chem. Rev. 1970, 5, 75.
https://doi.org/10.1016/S0010-8545(00)80075-2

12. Retsky K.L., Freeman M.W., Frei B. J. Biol. Chem. 1993, 268, 1304.
https://doi.org/10.1016/s0021-9258(18)54075-8

13. Kimura M., Yamamoto M., Yamabe S. J. Chem. Soc. Dalton Trans. 1982, 423.
https://doi.org/10.1039/DT9820000423

14. Espenson J.H. Chemical Kinetics and Reaction Mechanism. New York: McGraw-Hill, 1981. p 172.

15. Williams N.H., Yandell J.K. Aust. J. Chem. 1983, 36, 2377.
https://doi.org/10.1071/CH9832377

16. Marcus R.A. J. Phys. Chem. 1963, 67, 853.
https://doi.org/10.1021/j100798a033

17. Costas M., Mehn M.P., Jensen M.P., Que L. Chem. Rev. 2004, 109, 939.
https://doi.org/10.1021/cr020628n

18. Rajagopalon K.V. Adv. Enzymol. Relat. Areas Mol. Biol. 1991, 64, 215.
https://doi.org/10.1002/9780470123102.ch5

19. Sullivan E.P., Hazzard J.T., Tollin G., Enemark J.H. J. Am. Chem. Soc. 1992, 114, 9662.
https://doi.org/10.1021/ja00050a058

20. Chatterjee D. Trans. Met. Chem. 2000, 25, 227.
https://doi.org/10.1023/A:1007017008415

21. Sillén L.G., Martell A.E., Bjerrum J. Special Publication (Royal Society of Chemistry (Great Britain)) 1964, 17, 3711.

22. Rodrigenz A., Lopez S., Carmona C.G., Sanchez F. J. Chem. Soc. Dalton Trans. 1986, 1265.
https://doi.org/10.1039/DT9860001265

23. Saha S.H., Ghosh M.C., Banerjee P. J. Chem. Soc. Dalton Trans. 1986, 1301.
https://doi.org/10.1039/dt9860001301

24. Bhattacharya S., Ali M., Gangopadhyay S., Banerjee P. J. Chem. Soc. Dalton Trans. 1994, 3733.
https://doi.org/10.1039/DT9940003733

25. McAuley A., Macdonald C.J., Spencer L., West P.R. J. Chem. Soc. Dalton Trans. 1988, 2279.
https://doi.org/10.1039/dt9880002279

26. Akhtar M.J., Haim A. Inorg. Chem. 1988, 27, 1608.
https://doi.org/10.1021/ic00282a019

27. Creutz C. Inorg. Chem. 1981, 20, 4449.
https://doi.org/10.1021/ic50226a088

28. Li L., Rose P., Moore P.K. Annu. Rev. Pharmacol. 2011, 51, 169.
https://doi.org/10.1146/annurev-pharmtox-010510-100505

29. Kolluru G.K., Shen X., Kevil C.G. Redox Biol. 2013, 1, 313.
https://doi.org/10.1016/j.redox.2013.05.001

30. Chatterjee D., Jaiswal N., Sarkar P. Dalton Trans. 2015, 44, 7613.
https://doi.org/10.1039/C5DT00472A

31. Perrin D.D. Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution. Oxford: Pergamon Press, 1982.

32. Paulsen C.E., Carroll K.S. Chem. Rev. 2013, 113, 4633.
https://doi.org/10.1021/cr300163e

33. Chatterjee D., Pal U., Ghosh S., van Eldik R. Dalton Trans. 2015, 40, 1302.
https://doi.org/10.1039/c0dt01444c

34. van Eldik R., Gaede W., Wieland S., Kraft J., Spitzer M., Palmer D.A. Rev. Sci. Instrum. 1993, 64, 1355.
https://doi.org/10.1063/1.1144466

35. Sugiyama Y., Takahashi S., Ishimori K., Morishima I. J. Am. Chem. Soc. 1997, 119, 9582.
https://doi.org/10.1021/ja971138t

Attachment	Size
mhc190497c.pdf	1.08 MB

Журнал "Макрогетероциклы"

Navigation

Languages

News

Search

Electron Transfer Reactions of RuIII(edta) Containing the N-Heterocyclic Ligand Pyrazine: Kinetic and Mechanistic Studies

References: