Photocatalytic hydrogen evolution by a diiron hydrogenase model based on a peptide fragment of cytochrome c 556 with an attached diiron carbonyl cluster and an attached ruthenium photosensitizer

Journal of Inorganic Biochemistry

Volumn 108, Issue , 2012, Pages 159-162

  Sano, Yohei ^a   Onoda, Akira ^a   Hayashi, Takashi ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Cytochrome c 556; Diiron carbonyl cluster; Intramolecular electron transfer system; Photocatalytic hydrogen evolution

Indexed keywords

ASCORBIC ACID; CARBONYL IRON; CYTOCHROME C; CYTOCHROME C556; DIIRON HYDROGENASE; HISTIDINE; HYDROGEN; HYDROGENASE; PHOTOSENSITIZING AGENT; RUTHENIUM; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; CARBOXY TERMINAL SEQUENCE; CONFERENCE PAPER; ENZYME STRUCTURE; PH MEASUREMENT; PHOTOCATALYSIS;

CYSTEINE; CYTOCHROME C GROUP; HISTIDINE; HYDROGEN; HYDROGENASE; MODELS, MOLECULAR; PHOTOSENSITIZING AGENTS; RUTHENIUM;

EID: 84858440222     PISSN: 01620134     EISSN: 18733344     Source Type: Journal    
DOI: 10.1016/j.jinorgbio.2011.07.010     Document Type: Conference Paper

References (26)

1. R. Cammack, M. Frey, and R. Robson Hydrogen as a Fuel: Learning from Nature 2001 CRC Press Boca Raton, Florida
2. B.J. Lemon, and J.W. Peters A. Messershmidt, R. Huber, T. Poulos, K. Wieghardt, Handbook of Metalloproteins Vol. 2 2001 John Wiley & Sons, Ltd Chichester 738 751
3. J.W. Peters, W.N. Lanzilotta, B.J. Lemon, and L.C. Seefeldt Science 282 1998 1853 1858
4. Y. Nicolet, C. Piras, P. Legrand, C.E. Hatchikian, and J.C. Fontecilla-Camps Structure 7 1999 13 23
5. A.S. Pandey, T.V. Harris, L.J. Giles, J.W. Peters, and R.K. Szilagyi J. Am. Chem. Soc. 130 2008 4533 4540
6. C. Tard, X. Liu, S.K. Ibrahim, M. Bruschi, L.D. Gioia, S.C. Davies, X. Yang, L.-S. Wang, G. Sawers, and C.J. Pickett Nature 433 2005 610 613
7. A.K. Jones, B.R. Lichtenstein, A. Dutta, G. Gordon, and P.L. Dutton J. Am. Chem. Soc. 129 2007 14844 14845
8. M.L. Singleton, J.H. Reibenspies, and M.Y. Darensbourg J. Am. Chem. Soc. 132 2010 8870 8871
9. Y. Na, J. Pan, M. Wang, and L. Sun Inorg. Chem. 46 2007 3813 3815
10. Y. Na, M. Wang, J. Pan, P. Zhang, B. Åkermark, and L. Sun Inorg. Chem. 47 2008 2805 2810
11. D. Streich, Y. Astuti, M. Orlandi, L. Schwartz, R. Lomoth, L. Hammarström, and S. Ott Chem. Eur. J. 16 2010 60 63
12. P. Zhang, M. Wang, Y. Na, X. Li, Y. Jiang, and L. Sun Dalton Trans. 39 2010 1204 1206
13. F. Wang, W.-G. Wang, W.-J. Wang, H.-Y. Wang, C.-H. Tung, and L.-Z. Wu Angew. Chem. Int. Ed. 50 2011 3193 3197
14. Y. Sano, A. Onoda, and T. Hayashi Chem. Commun. 47 2011 8229 8231
15. L. Sun, B. Åkermark, and S. Ott Coord. Chem. Rev. 249 2005 1653 1663
16. S. Ott, M. Kritikos, B. Åkermark, and L. Sun Angew. Chem. Int. Ed. 42 2003 3285 3288
17. H. Wolpher, M. Borgström, L. Hammarström, J. Bergquist, V. Sundström, S. Styring, L. Sun, and B. Åkermark Inorg. Chem. Commun. 6 2003 989 991
18. J. Ekström, M. Abrahamsson, C. Olson, J. Bergquist, F.B. Kaynak, L. Eriksson, L. Sun, H.-C. Becker, B. Åkermark, L. Hammarström, and S. Ott Dalton Trans. 35 2006 4599 4606
19. L.-C. Song, M.-Y. Tang, S.-Z. Mei, J.-H. Huang, and Q.-M. Hu Organometallics 26 2007 1575 1577
20. X. Li, M. Wang, S. Zhang, J. Pan, Y. Na, J. Liu, B. Åkermark, and L. Sun J. Phys Chem. B 112 2008 8198 8202
21. A.M. Kluwer, R. Kapre, F. Hartl, M. Lutz, A.L. Spek, A.M. Brouwer, P.W.N.M. van Leeuwen, and J.N.H. Reek Proc. Natl. Acad. Sci. U. S. A. 106 2009 10460 10465
22. A.P.S. Samuel, D.T. Co, C.L. Stern, and M.R. Wasielewski J. Am. Chem. Soc. 132 2010 8813 8815
23. X.-J. Yang, F. Drepper, B. Wu, W.-H. Sun, W. Haehnel, and C. Janiak Dalton Trans. 34 2005 256 267
24. M. Montalti, S. Wadhwa, W.Y. Kim, R.A. Kipp, and R.H. Schmehl Inorg. Chem. 39 2000 76 84
25. M. Hass, S.-X. Liu, A. Kahnt, C. Leiggener, D.M. Guldi, A. Hauser, and S. Decurtins J. Org. Chem. 72 2007 7533 7543
26. R.M. Berger, and D.R. McMillin Inorg. Chem. 27 1988 4245 4249