Electrochemical investigation into the electron transfer mechanism of a diiron hexacarbonyl complex bearing a bridging naphthalene moiety

Electrochimica Acta

Volumn 163, Issue , 2015, Pages 190-195

  Qian, Guifen ^a   Wang, Hailong ^b   Zhong, Wei ^b   Liu, Xiaoming ^a,b  

^a NANCHANG UNIVERSITY   (China)

^b JIAXING UNIVERSITY   (China)

Author keywords

derivatives of 1,8 naphthalenedithiolate; diiron carbonyl complex; Electron transfer mechanism; FeFe hydrogenase

Indexed keywords

CHEMICAL REACTIONS; DICHLOROMETHANE; ELECTRON TRANSITIONS; ELECTRONS; NAPHTHALENE;

CARBONYL COMPLEXES; CHEMICAL REDUCTION; ELECTROCHEMICAL INVESTIGATIONS; ELECTRON TRANSFER MECHANISMS; FERROCENYL GROUPS; HEXACARBONYL COMPLEX; NAPHTHALENE MOIETIES; [FEFE]HYDROGENASES;

REDUCTION;

EID: 84923558080     PISSN: 00134686     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.electacta.2015.02.163     Document Type: Article

References (35)

1. J.W. Peters, W.N. Lanzilotta, B.J. Lemon, and L.C. Seefeldt X-ray crystal structure of the Fe-only hydrogenase (Cpl) from Clostridium pasteurianum to 1.8 angstrom resolution Science 282 1998 1853 1858
2. Y. Nicolet, C. Piras, P. Legrand, C.E. Hatchikian, and J.C. Fontecilla-Camps Desulfovibrio desulfuricans iron hydrogenase: the structure shows unusual coordination to an active site Fe binuclear center Structure with Folding & Design 7 1999 13 23
3. S.P. Best Spectroelectrochemistry of hydrogenase enzymes and related compounds Coord. Chem. Rev. 249 2005 1536 1554
4. 2 evolution by di-iron sub-site models Coord. Chem. Rev. 249 2005 1664 1676
5. F. Gloaguen, D. Morvan, J.F. Capon, P. Schollhammer, and J. Talarmin Electrochemical proton reduction at mild potentials by monosubstituted diiron organometallic complexes bearing a benzenedithiolate bridge J. Electroanal. Chem. 603 2007 15 20
6. 2 ase C. R. Chim. 11 2008 842 851
7. J.F. Capon, F. Gloaguen, F.Y. Petillon, P. Schollhammer, and J. Talarmin Electron and proton transfers at diiron dithiolate sites relevant to the catalysis of proton reduction by the FeFe-hydrogenases Coord. Chem. Rev. 253 2009 1476 1494
8. G.A.N. Felton, C.A. Mebi, B.J. Petro, A.K. Vannucci, D.H. Evans, R.S. Glass, and D.L. Lichtenberger Review of electrochemical studies of complexes containing the Fe2S2 core characteristic of FeFe-hydrogenases including catalysis by these complexes of the reduction of acids to form dihydrogen J. Organomet. Chem. 694 2009 2681 2699
9. Y.W. Wang, Z.M. Li, X.H. Zeng, X.F. Wang, C.X. Zhan, Y.Q. Liu, X.R. Zeng, Q.Y. Luo, and X.M. Liu Synthesis and characterisation of three diiron tetracarbonyl complexes related to the diiron centre of [FeFe]-hydrogenase and their protonating, electrochemical investigations New J. Chem. 33 2009 1780 1789
10. X.H. Zeng, Z.M. Li, Z.Y. Xiao, Y.W. Wang, and X.M. Liu Using pendant ferrocenyl group(s) as an intramolecular standard to probe the reduction of diiron hexacarbonyl model complexes for the sub-unit of [FeFe]-hydrogenase Electrochem. Commun. 12 2010 342 345
11. S.P. Best, S.J. Borg, J.M. White, M. Razavet, and C.J. Pickett On the structure of a proposed mixed-valent analogue of the diiron subsite of [FeFe]-hydrogenase Chem. Commun. 2007 4348 4350
12. S.J. Borg, T. Behrsing, S.P. Best, M. Razavet, X. Liu, and C.J. Pickett Electron Transfer at a Dithiolate-Bridged Diiron Assembly: Electrocatalytic Hydrogen Evolution J. Am. Chem. Soc. 126 2004 16988 16999
13. G.A.N. Felton, A.K. Vannucci, J. Chen, L.T. Lockett, N. Okumura, B.J. Petro, U.I. Zakai, D.H. Evans, R.S. Glass, and D.L. Lichtenberger Hydrogen Generation from Weak Acids: Electrochemical and Computational Studies of a Diiron Hydrogenase Mimic J. Am. Chem. Soc. 129 2007 12521 12530
14. 6]: The Simplest Functional Model of the Fe-Hydrogenase Active Site Inorg. Chem. 46 2007 108 116
15. I.A. de Carcer, A. DiPasquale, A.L. Rheingold, and D.M. Heinekey Active-site models for iron hydrogenases: Reduction chemistry of dinuclear iron complexes Inorg. Chem. 45 2006 8000 8002
16. (n)](n = 0, 2) complexes related to the FeFe-hydrogenase active site C. R. Chim. 11 2008 875 889
17. L. Schwartz, J. Ekstrom, R. Lomoth, and S. Ott Dynamic ligation at the first amine-coordinated iron hydrogenase active site mimic Chem. Commun. 2006 4206 4208
18. 6 Complexes with Competing Ligands Eur. J. Inorg. Chem. 2011 1106 1111
19. R.J. Wright, C. Lim, and T.D. Tilley Diiron Proton Reduction Catalysts Possessing Electron-Rich and Electron-Poor Naphthalene-1,8-dithiolate Ligands Chem. Eur. J. 15 2009 8518 8525
20. A.P.S. Samuel, D.T. Co, C.L. Stern, and M.R. Wasielewski Ultrafast Photodriven Intramolecular Electron Transfer from a Zinc Porphyrin to a Readily Reduced Diiron Hydrogenase Model Complex J. Am. Chem. Soc. 132 2010 8813 8815
21. P.S. Singh, H.C. Rudbeck, P. Huang, S. Ezzaher, L. Eriksson, M. Stein, S. Ott, and R. Lomoth (I,0) Mixed-Valence State of a Diiron Complex with Pertinence to the [FeFe]-Hydrogenase Active Site: An IR, EPR, and Computational Study Inorg. Chem. 48 2009 10883 10885
22. Z.Y. Xiao, Z.H. Wei, L. Long, Y.L. Wang, D.J. Evans, and X.M. Liu Diiron carbonyl complexes possessing a {Fe(II)Fe(II)} core: synthesis, characterisation, and electrochemical investigation Dalton Trans. 40 2011 4291 4299
23. n (n = 12, 11, 10, 9) J. Am. Chem. Soc. 128 2006 11376 11384
24. A.M. Royer, T.B. Rauchfuss, and D.L. Gray Oxidative Addition of Thioesters to Iron(0): Active-Site Models for Hmd Nature's Third Hydrogenase Organometallics 28 2009 3618 3620
25. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, J.A. Montgomery Jr., T. Vreven, K.N. Kudin, J.C. Burant, J.M. Millam, S.S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G.A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J.E. Knox, H.P. Hratchian, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, P.Y. Ayala, K. Morokuma, G.A. Voth, P. Salvador, J.J. Dannenberg, V.G. Zakrzewski, S. Dapprich, A.D. Daniels, M.C. Strain, O. Farkas, D.K. Malick, A.D. Rabuck, K. Raghavachari, J.B. Foresman, J.V. Ortiz, Q. Cui, A.G. Baboul, S. Clifford, J. Cioslowski, B.B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R.L. Martin, D.J. Fox, T. Keith, M.A. Al-Laham, C.Y. Peng, A. Nanayakkara, M. Challacombe, P.M.W. Gill, B. Johnson, W. Chen, M.W. Wong, C. Gonzalez, and J.A. Pople Gaussian 03, Revision E.01 2003 Gaussian Inc. Wallingford, CT
26. A.D. Becke Density-functional exchange-energy approximation with correct asymptotic behavior Phys. Rev. A 38 1988 3098 3100
27. J.P. Perdew Density-functional approximation for the correlation energy of the inhomogeneous electron gas Phys. Rev. B 33 1986 8822 8824
28. N. Leidel, C.-H. Hsieh, P. Chernev, K.G.V. Sigfridsson, M.Y. Darensbourg, and M. Haumann Bridging-hydride influence on the electronic structure of an [FeFe]-hydrogenase active-site model complex revealed by XAES-DFT Dalton Trans. 42 2013 7539 7554
29. J. Li, C.L. Fisher, J.L. Chen, D. Bashford, and L. Noodleman Calculation of Redox Potentials and pKa Values of Hydrated Transition Metal Cations by a Combined Density Functional and Continuum Dielectric Theory Inorg. Chem. 35 1996 4694 4702
30. E.W. Miller, S.X. Bian, and C.J.R.N. Chang A fluorescent sensor for imaging reversible redox cycles in living cells J. Am. Chem. Soc. 129 2007 3458 3459
31. C. Topf, U. Monkowius, and G. Knoer Design, synthesis and characterization of a modular bridging ligand platform for bio-inspired hydrogen production Inorg. Chem. Commun. 21 2012 147 150
32. A.J. Ashe, J.W. Kampf, and P.M. Savla The reaction of sulfur with dilithio compounds. The syntheses and structures of phenanthro [1,10-cd]-1,2-dithiole and phenanthro[4,5-cde] [1,2]dithiin Heteroat. Chem. 5 1994 113 119
33. L. Chen, M. Wang, F. Gloaguen, D. Zheng, P. Zhang, and L. Sun Multielectron-Transfer Templates via Consecutive Two-Electron Transformations: Iron-Sulfur Complexes Relevant to Biological Enzymes Chem. Eur. J. 18 2012 13968 13973
34. P.S. Singh, H.C. Rudbeck, P. Huang, S. Ezzaher, L. Eriksson, M. Stein, S. Ott, and R. Lomoth (I,0) Mixed-Valence State of a Diiron Complex with Pertinence to the [FeFe]-Hydrogenase Active Site: An IR, EPR, and Computational Study Inorg. Chem. 48 2009 10883 10885
35. Y. Tang, Z.H. Wei, W. Zhong, and X.M. Liu Diiron Complexes with Pendant Phenol Group(s) as Mimics of the Diiron Subunit of [FeFe]-Hydrogenase: Synthesis, Characterisation, and Electrochemical Investigation Eur. J. Inorg. Chem. 2011 1112 1120