Photoinduced electron transfer in donor-bridge-acceptor assemblies: The case of Os(II)-bis(terpyridine)-(bi)pyridinium dyads

Coordination Chemistry Reviews

Volumn 304-305, Issue , 2015, Pages 109-116

  Arrigo, Antonino ^a   Santoro, Antonio ^a   Puntoriero, Fausto ^a   Lainé, Philippe P ^b   Campagna, Sebastiano ^a,c  

^a UNIVERSITY OF MESSINA   (Italy)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c Istituto Per La Sintesi Organica E La Fotoreattività   (Italy)

Author keywords

Charge recombination; Charge separation; Equilibrated states; Molecular dyads; Os(II) polypyridine complexes; Photoinduced electron transfer

Indexed keywords

EID: 84940448028     PISSN: 00108545     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ccr.2014.09.019     Document Type: Review

References (73)

1. Hambourger M., Moore G.F., Kramer D.M., Gust D., Moore A.L., Moore T.A. Chem. Soc. Rev. 2009, 38:25.
2. Energy Information Association, U.S. Department of Energy, Washington DC. 〈www.eia.doe.gov〉 (accessed January 2010).
3. Cook T.R., Dogutan D.K., Reece S.Y., Surendranath Y., Teets T.S., Nocera D.G. Chem. Rev. 2010, 110:6474.
4. Summary for Policy Makers 2007, IPCC, Cambridge University Press, Cambridge, UK, and New York, NY, USA.
5. Armaroli N., Balzani V. Angew. Chem. Int. Ed. 2007, 46:52.
6. Huynh M.H.V., Meyer T.J. Chem. Rev. 2007, 107:5004.
7. McEvoy J.P., Brudvig G.W. Chem. Rev. 2006, 106:4455.
8. Wasielewski M. Acc. Chem. Res. 2009, 42:1910.
9. Gust D., Moore A.L. Acc. Chem. Res. 2009, 42:1890.
10. Herrero C., Quaranta A., Leibl W., Rutherford A.W., Aukauloo A. Energy Environ. Sci. 2011, 4:2353.
11. Armaroli N., Balzani V. Energy for a Sustainable World 2011, Wiley-VCH, Weinheim.
12. Bard A.J., Fox M.A. Acc. Chem. Res. 1995, 28:141.
13. Lewis N.S., Nocera D.G. Proc. Natl. Acad. Sci. USA 2006, 103:15729.
14. Gray H.B. Nat. Chem. 2009, 1:7.
15. Sherman B.D., Vaughn M.D., Bergkamp J.J., Gust D., Moore A.L., Moore T.A. Photosynth. Res. 2014, 120:59.
16. Meyer T.J. Nature 2008, 451:778.
17. Liu F., Conception J.J., Jurss J.W., Cardolaccia T., Templeton J.L., Meyer T.J. Inorg. Chem. 2008, 47:1727.
18. Jurss J.W., Concepcion J.C., Norris M.R., Templeton J.L., Meyer T.J. Inorg. Chem. 2010, 49:3980.
19. Kohler L., Kaveevivitchai N., Zong R., Thummel R.P. Inorg. Chem. 2014, 53:912.
20. Arachchige S.M., Brewer K.J. Energy Production and Storage Inorganic Chemical Strategies for a Warming World 2010, 143-171. John Wiley & Sons, Chichester, West Sussex, UK. R. Crabtree (Ed.).
21. Teets T.S., Nocera D.G. Chem. Comm. 2011, 47:9268.
22. Wang F., Wang W.G., Wang H.Y., Si G., Tung C.H., Wu L.Z. ACS Catal. 2012, 2:407.
23. The Hydrogen Economy: Opportunities, Costs, Barriers, and R&D Needs, 2004, U.S. National Research Council and U.S. National Academy of Engineering.
24. Gust D., Moore T.A., Moore A.L. Faraday Disc. 2012, 155:9.
25. Balzani V., Campagna S., Denti G., Juris A., Serroni S., Venturi M. Acc. Chem. Res. 1998, 31:26.
26. Balzani V., Serroni S. Sci. Spectra 2000, 26.
27. Huynh M.H.V., Dattelbaum D.M., Meyer T.J. Coord. Chem. Rev. 2005, 249:457.
28. Balzani V., Credi A., Venturi M. Molecular Devices and Machines: Concepts and Perspectives for the Nanoworld 2008, Wiley-VCH, Weinheim, (ch. 3. The literature on this topic is too large to be exhaustively quoted). 2nd edn.
29. Fukuzumi S. Bull. Chem. Soc. Jpn. 2006, 79:177.
30. Wasielewski M.R. J. Org. Chem. 2006, 71:5051.
31. Albinsson B., Mårtensson J. J. Photochem. Photobiol. C 2008, 9:138.
32. Gust D., Moore T.A., Moore A.L. Acc. Chem. Res. 2001, 34:40.
33. Wenger O.S. Acc. Chem. Res. 2011, 44:25.
34. Taylor J., Davies E.S., Weinstein J.A., Sazanovich I.V., Bouganov O.V., Tikhomirov S.A., Towrie M., McAster J., Garner C.D. Inorg. Chem. 2012, 51:13181.
35. Sazanovich I.V., Alamiry M.A.H., Meijer A.J.H.M., Towrie M., Davies E.S., Bennet R.D., Weinstein J.A. Pure Appl. Chem. 2013, 85. (and refs. therein 1331).
36. Balzani V., Ceroni P., Juris A. Photochemistry and Photophysics: Concepts, Research, Perspectives 2014, Wiley-VCH, Weinheim.
37. Fortage J., Dupeyre G., Tuyèras F., Marvaud V., Ochsenbein P., Ciofini I., Hromadová M., Pospísil L., Arrigo A., Trovato E., Puntoriero F., Lainé P.P., Campagna S. Inorg. Chem. 2013, 52:11944. (and refs therein).
38. Fortage J., Puntoriero F., Tuyèras F., Dupeyre G., Arrigo A., Ciofini I., Lainé P.P., Campagna S. Inorg. Chem. 2012, 51:5342.
39. Paddon-Row M.N. Electron Transfer in Chemistry 2001, 3:p179. Wiley-VCH, Weinheim.
40. Juris A., Balzani V., Barigelletti F., Campagna S., Belser P., Von Zelewsky A. Coord. Chem. Rev. 1988, 84:85.
41. Meyer T.J. Acc. Chem. Res. 1989, 22:163.
42. Sauvage J.P., Collin J.P., Chambron J.C., Guillerez S., Coudret C., Balzani V., Barigelletti F., De Cola L., Flamigni L. Chem. Rev. 1994, 94:993.
43. Balzani V., Juris A., Venturi M., Campagna S., Serroni S. Chem. Rev. 1996, 96:759.
44. Campagna S., Puntoriero F., Nastasi F., Bergamini G., Balzani V. Top. Curr. Chem. 2007, 280:117.
45. Sutin N., Brunschwing B.S. ACS Symp. Ser. 1982, 198:105.
46. Bonin J., Costentin C., Robert M., Routier M., Savéant J.-M. J. Am. Chem. Soc. 2013, 135:14359.
47. Gaines G.L., O'Neil M.P., Svec W.A., Niemczyk M.P., Wasielewski M.R. J. Am. Chem. Soc. 1991, 113:719.
48. Chen P., Meyer T.J. Chem. Rev. 1998, 98:1439.
49. McConnell H.M. J. Chem. Phys. 1961, 35:508.
50. Jordan K.D., Paddon-Row M.N. Chem. Rev. 1992, 92:395.
51. Reimers J.R., Hush N.S. J. Photochem. Photobiol. A: Chem. 1994, 82:31.
52. Meyer T.J. Pure Appl. Chem. 1986, 58:1193.
53. Barbara P.F., Meyer T.J., Ratner M.A. J. Phys. Chem. 1996, 100:13148.
54. Miller J.R., Beitz J.V., Huddleston R.K. J. Am. Chem. Soc. 1984, 106:5057.
55. Marcus R.A., Sutin N. Biochim. Biophys. Acta 1985, 811:265.
56. Natali M., Campagna S., Scandola F. Chem. Soc. Rev. 2014, 43:4005.
57. Arrigo A., Santoro A., Indelli M.T., Natali M., Scandola F., Campagna S. Phys. Chem. Chem. Phys. 2014, 16:818.
58. Indelli M.T., Orlandi M., Chiorboli C., Ravaglia M., Scandola F., Lafolet F., Welter S., De Cola L. J. Phys. Chem. A 2012, 116:119.
59. De Cola L., Balzani V., Barigelletti F., Flamigni L., Belser P., von Zelewsky A., Franck M., Vögtle F. Inorg. Chem. 1993, 32:5228.
60. Heitele H., Finckh P., Weeren S., Pöllinger F., Michel-Beyerle M.E. J. Phys. Chem. 1989, 93:5173.
61. Kuciauskas D., Liddell P.A., Lin S., Stone S.G., Moore A.L., Moore T.A., Gust D. J. Phys. Chem. B 2000, 104:4307.
62. Yamazaki M., Araki Y., Fujitsuka M., Ito O. J. Phys. Chem. A 2001, 105:8615.
63. Cotlet M., Masuo S., Luo G., Hofkens J., Van der Auweraer M., Verhoeven J.K., Müllen X.S., Xie F., De Schryver Proc. Natl. Acad. Sci. USA 2004, 101:14343.
64. Kawauchi H., Suzuki S., Kozaki M., Okada K., Islam D.-M.S., Araki Y., Ito O., Yamanaka K.J. Phys. Chem. A 2008, 112:5878.
65. Ren G., Schlenker C.W., Ahmed E., Subramaniyan S., Olthor S., Kahn A., Ginger D.S., Jenekhe S.A. Adv. Funct. Mater. 2013, 23:1238.
66. Borgström M., Johansson O., Lomoth R., Berglund Baudin H., Wallin S., Sun L., Åkermark B., Hammarström L. Inorg. Chem. 2003, 42:5173.
67. Hanss D., Wenger O.S. Eur. J. Inorg. Chem. 2009, 3778.
68. Lainé P., Amouyal E. Chem. Commun. 1999, 935.
69. Lainé P., Bedioui F., Amouyal E., Albin V., Berruyer-Penaud F. Chem. Eur. J. 2002, 8:3162.
70. Ciofini I., Lainé P.P., Bedioui F., Adamo C. J. Am. Chem. Soc. 2004, 126:10763.
71. Lainé P.P., Ciofini I., Ochsenbein P., Amouyal E., Adamo C., Bedioui F. Chem. Eur. J. 2005, 11:3711.
72. In fact, the charge-separated states in 4 and 5 have relatively high energies, so that back electron transfer to the ground state is expected to occur in the Marcus inverted region and can be relatively slow. From an electronic viewpoint, charge recombination to the 3MLCT state, i.e. the process denoted as EQ in Fig. 6, involves orbitals that are spatially close to one another, whereas charge recombination to the ground state (CR in Fig. 6) would involve a metal-centered orbital as the acceptor partner, with a reduced electronic coupling for the process as compared with EQ and CS processes. A cursory look at Fig. 6a should better clarify this issue.
73. Lainé P.P., Campagna S., Loiseau F. Coord. Chem. Rev. 2008, 252:2552.