Transition Metal Chemistry

, Volume 37, Issue 7, pp 645–650 | Cite as

Iron(I)-carbonyl clusters tethered to (trifluoromethyl)thiophenolates

  • Charles A. Mebi
  • Joshua J. Trujillo
  • Britney L. Rosenthal
  • Robert B. Bowman
  • Bruce C. Noll
  • Patrick J. Desrochers
Article

Abstract

Two diironhexacarbonyl clusters containing (trifluoromethyl)thiophenolates, as models for the active site of [Fe–Fe] hydrogenase enzyme, have been prepared and characterized. The crystal and electronic structures of the complexes have been probed by X-ray crystallography and spectroscopic methods. Cyclic voltammetric studies in the presence of acetic acid show that both compounds catalyze the electrochemical reduction of acetic acid to produce hydrogen with favorable overpotentials.

Keywords

Glassy Carbon Electrode Trifluoromethyl Diiron Carbonyl Cluster Cyclic Voltammetric Study 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

The authors gratefully acknowledge support for this work from Arkansas Tech University. P. J. D. gratefully acknowledges the National Science Foundation (Grant CCLI 0125711) for funding the NMR used for this work.

References

  1. 1.
    Gratzel M (1981) Acc Chem Res 14:376–384CrossRefGoogle Scholar
  2. 2.
    Lewis NS, Nocera DG (2006) Proc Natl Acad Sci USA 103:15729–15735CrossRefGoogle Scholar
  3. 3.
    Capon J-F, Gloaguen F, Petillon FY, Schollhammer P, Talarmin J (2009) Coord Chem Rev 253:1476–1494CrossRefGoogle Scholar
  4. 4.
    Gloaguen F, Rauchfuss TB (2009) Chem Soc Rev 38:100–108CrossRefGoogle Scholar
  5. 5.
    Peters JW, Lanzilotta WN, Lemon BJ, Seefeldt LC (1998) Science 282:1853–1858CrossRefGoogle Scholar
  6. 6.
    Daraosheh AQ, Apfel U-P, Görls H, Friebe C, Schubert US, El-khateeb M, Mloston G, Weigand W (2012) Eur J Inorg Chem 2012:318–326Google Scholar
  7. 7.
    Mebi CA, Brigance KE, Bowman RB (2012) J Braz Chem Soc 23:186–189CrossRefGoogle Scholar
  8. 8.
    Durgaprasad G, Bolligarla R, Das SK (2011) J Organomet Chem 696:3097–3105CrossRefGoogle Scholar
  9. 9.
    Mousser H, Darchen A, Mousser A (2010) J Organomet Chem 695:786–791CrossRefGoogle Scholar
  10. 10.
    Wright RJ, Lim C, Tilley TD (2009) Chem Eur J 15:8518–8525CrossRefGoogle Scholar
  11. 11.
    Mebi CA, Noll BC, Gao R, Karr DZ (2010) Anorg Allg Chem 636:2550–2554CrossRefGoogle Scholar
  12. 12.
    Song L-C, Ge J-H, Liu X-F, Zhao L-Q, Hu Q-M (2006) J Organomet Chem 691:5701–5709CrossRefGoogle Scholar
  13. 13.
    Felton GA, Mebi CA, Petro BJ, Vannucci AK, Evans DH, Glass RS, Lichtenberger DL (2009) J Organomet Chem 694:2681–2699CrossRefGoogle Scholar
  14. 14.
    Mebi CA, Karr DS, Gao R (2011) J Coord Chem 64:4397–4407CrossRefGoogle Scholar
  15. 15.
    Yu Z, Wang M, Li P, Dong W, Wang F, Sun L (2008) Dalton Trans 2400–2406Google Scholar
  16. 16.
    Sheldrick GM (2008) Acta Crystallogr A64:112–122Google Scholar
  17. 17.
    Tidwell CP, Bharara P, Rudeseal G, Rudeseal T, Rudeseal FH Jr, Simmer CA, McMillan D, Lanier K, Fondren LD, Folmar LL, Belmore K (2007) Molecules 12:1389–1398CrossRefGoogle Scholar
  18. 18.
    Zhen-Hong W, Xiu-Li Y, Ying T, Zhi-Yin X (2012) Chin J Struct Chem 31:122–126Google Scholar
  19. 19.
    Song L-C, Yang Z-Y, Bian H-Z, Liu Y, Wang H-T, Liu X-F, Hu Q-M (2005) Organometallics 24:6126–6135CrossRefGoogle Scholar
  20. 20.
    Razavet M, Davies SC, Hughes DL, Barclay JE, Evans DJ, Fairhurst SA, Liu X, Pickett CJ (2003) Dalton Trans 586–595Google Scholar
  21. 21.
    Si Y, Hu M, Chen C (2008) C R Chimie 11:932–937CrossRefGoogle Scholar
  22. 22.
    Felton GA, Glass RS, Lichtenberger DL, Evans DH (2006) Inorg Chem 45:9181–9184CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2012

Authors and Affiliations

  • Charles A. Mebi
    • 1
  • Joshua J. Trujillo
    • 1
  • Britney L. Rosenthal
    • 1
  • Robert B. Bowman
    • 1
  • Bruce C. Noll
    • 2
  • Patrick J. Desrochers
    • 3
  1. 1.Department of Physical Sciences, College of Natural and Health SciencesArkansas Tech UniversityRussellvilleUSA
  2. 2.Bruker AXS Inc.MadisonUSA
  3. 3.Department of ChemistryUniversity of Central ArkansasConwayUSA

Personalised recommendations