Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light

ChemCatChem

Volumn 7, Issue 20, 2015, Pages 3316-3321

  Rosas Hernández, Alonso ^a   Junge, Henrik ^a   Beller, Matthias ^a  

^a UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

homogeneous catalysis; iridium; photochemistry; ruthenium; structure activity relationships

Indexed keywords

BENZENE REFINING; CARBON; CARBON DIOXIDE; CATALYSIS; CATALYST SELECTIVITY; CATALYSTS; FORMIC ACID; IRIDIUM; LIGHT; PHOTOCHEMICAL REACTIONS; PHOTOSENSITIZERS; REDOX REACTIONS; RUTHENIUM; SELECTIVE CATALYTIC REDUCTION;

ELECTRON TRANSFER; HOMOGENEOUS CATALYSIS; PHOTOCATALYTIC REACTIONS; PHOTOCATALYTIC SYSTEMS; PHOTOCHEMICAL REDUCTION; SELECTIVE REDUCTION; STRUCTURE ACTIVITY RELATIONSHIPS; VISIBLE-LIGHT IRRADIATION;

CATALYST ACTIVITY;

EID: 84944174439     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201500494     Document Type: Article

References (70)

1. G. Centi, E. A. Quadrelli, S. Perathoner, Energy Environ. Sci. 2013, 6, 1711;
2. A. Corma, H. García, J. Catal. 2013, 308, 168;
3. E. B. Cole, A. B. Bocarsly, in Carbon Dioxide as Chemical Feedstock (Ed.:, M. Aresta,), Wiley-VCH, Weinheim, 2010, pp. 291-316.
4. T. Inoue, A. Fujishima, S. Konishi, K. Honda, Nature 1979, 277, 637.
5. S. N. Habisreutinger, L. Schmidt-Mende, J. K. Stolarczyk, Angew. Chem. Int. Ed. 2013, 52, 7372;
6. Angew. Chem. 2013, 125, 7516;
7. S. Navalõn, A. Dhakshinamoorthy, H. G. M. Alvaro, ChemSusChem 2013, 6, 562;
8. A. Dhakshinamoorthy, S. Navalon, A. Corma, H. Garcia, Energy Environ. Sci. 2012, 5, 9217.
9. C. D. Windle, R. N. Perutz, Coord. Chem. Rev. 2012, 256, 2562;
10. H. Takeda, O. Ishitani, Coord. Chem. Rev. 2010, 254, 346;
11. A. J. Morris, G. J. Meyer, E. Fujita, Acc. Chem. Res. 2009, 42, 1983. For recent studies see:
12. H. Takeda, H. Koizumi, K. Okamoto, O. Ishitani, Chem. Commun. 2014, 50, 1491;
13. J. Bonin, M. Robert, M. Routier, J. Am. Chem. Soc. 2014, 136, 16768;
14. J. Bonin, M. Chaussemier, M. Robert, M. Routier, ChemCatChem 2014, 6, 3200;
15. K. Kobayashi, T. Kikuchi, S. Kitagawa, K. Tanaka, Angew. Chem. Int. Ed. 2014, 53, 11813;
16. Angew. Chem. 2014, 126, 12007;
17. S. Wang, W. Yao, J. Lin, Z. Ding, X. Wang, Angew. Chem. Int. Ed. 2014, 53, 1034.
18. T. Yui, Y. Tamaki, K. Sekizawa, O. Ishitani, Top. Curr. Chem. 2011, 303, 151;
19. H. Takeda, K. Koike, H. Inoue, O. Ishitani, J. Am. Chem. Soc. 2008, 130, 2023.
20. Y. Izumi, Coord. Chem. Rev. 2013, 257, 171;
21. S. Bensaid, G. Centi, E. Garrone, S. Perathoner, G. Saracco, ChemSusChem 2012, 5, 500;
22. Y. Amao, ChemCatChem 2011, 3, 458;
23. C. Herrero, A. Quaranta, W. Leibl, A. W. Rutherford, A. Aukauloo, Energy Environ. Sci. 2011, 4, 2353.
24. J.-M. Lehn, R. Ziessel, Proc. Natl. Acad. Sci. USA 1982, 79, 701.
25. J. L. Grant, K. Goswami, L. O. Spreer, J. W. Otvos, M. Calvin, J. Chem. Soc. Dalton Trans. 1987, 2105.
26. R. Zeisel, J.-M. Lehn, J. Organomet. Chem. 1990, 382, 157.
27. S. Matsuoka, K. Yamamoto, T. Ogata, M. Kusaba, N. Nakashima, E. Fujita, S. Yanagida, J. Am. Chem. Soc. 1993, 115, 601.
28. Y. Tamaki, T. Morimoto, K. Koike, O. Ishitani, Proc. Natl. Acad. Sci. USA 2012, 109, 15673;
29. S. Sato, K. Koike, H. Inoue, O. Ishitani, Photochem. Photobiol. Sci. 2007, 6, 454.
30. V. S. Thoi, N. Kornienko, C. G. Margarit, P. Yang, C. J. Chang, J. Am. Chem. Soc. 2013, 135, 14413.
31. J. Hawecker, J.-M. Lehn, R. Ziessel, J. Chem. Soc. Chem. Commun. 1983, 536.
32. S. Sato, T. Morikawa, T. Kajino, O. Ishitani, Angew. Chem. Int. Ed. 2013, 52, 988;
33. Angew. Chem. 2013, 125, 1022.
34. J. Hawecker, J.-L. Lehn, R. Ziessel, J. Chem. Soc. Chem. Commun. 1985, 56.
35. S.-P. Luo, E. Mejia, A. Friedrich, A. Pazidis, H. Junge, A.-E. Surkus, R. Jackstell, S. Denurra, S. Gladiali, S. Lochbrunner, M. Beller, Angew. Chem. Int. Ed. 2013, 52, 419;
36. Angew. Chem. 2013, 125, 437;
37. F. Gärtner, S. Denurra, S. Losse, A. Neubauer, A. Boddien, A. Gopinathan, A. Spannenberg, H. Junge, S. Lochbrunner, M. Blug, S. Hoch, J. Busse, S. Gladiali, M. Beller, Chem. Eur. J. 2012, 18, 3220;
38. F. Gärtner, D. Cozzula, S. Losse, A. Boddien, G. Anilkumar, H. Junge, T. Schulz, N. Marquet, A. Spannenberg, S. Gladiali, M. Beller, Chem. Eur. J. 2011, 17, 6998.
39. S. Moret, P. J. Dyson, G. Laurenczy, Dalton Trans. 2013, 42, 4353;
40. W. Gan, D. J. M. Snelders, P. J. Dyson, G. Laurenczy, ChemCatChem 2013, 5, 1126;
41. I. Mellone, M. Peruzzini, L. Rosi, D. Mellmann, H. Junge, M. Beller, L. Gonsalvi, Dalton Trans. 2013, 42, 2495;
42. P. Sponholz, D. Mellmann, H. Junge, M. Beller, ChemSusChem 2013, 6, 1172;
43. A. Boddien, D. Mellmann, F. Gärtner, R. Jackstell, H. Junge, P. J. Dyson, G. Laurenczy, R. Ludwig, M. Beller, Science 2011, 333, 1733.
44. Y.-J. Yuan, Z.-T. Yu, X.-Y. Chen, J.-Y. Zhang, Z.-G. Zou, Chem. Eur. J. 2011, 17, 12891;
45. F. Gärtner, B. Sundararaju, A.-E. Surkus, A. Boddien, B. Loges, H. Junge, P. H. Dixneuf, M. Beller, Angew. Chem. Int. Ed. 2009, 48, 9962;
46. Angew. Chem. 2009, 121, 10147;
47. P. N. Curtin, L. L. Tinker, C. M. Burgess, E. D. Cline, S. Bernhard, Inorg. Chem. 2009, 48, 10498;
48. L. L. Tinker, N. D. McDaniel, P. N. Curtin, C. K. Smith, M. J. Ireland, S. Bernhard, Chem. Eur. J. 2007, 13, 8726;
49. J. I. Goldsmith, W. R. Hudson, M. S. Lowry, T. H. Anderson, S. Bernhard, J. Am. Chem. Soc. 2005, 127, 7502.
50. A. Dovletoglou, S. A. Adeyemi, T. J. Meyer, Inorg. Chem. 1996, 35, 4120;
51. M. G. Colombo, A. Hauser, H. U. Gudel, Inorg. Chem. 1993, 32, 3088.
52. B. P. Sullivan, D. J. Salmon, T. J. Meyer, Inorg. Chem. 1978, 17, 3334.
53. A. J. Cruz, R. Kirgan, K. Siam, P. Heiland, D. P. Rillema, Inorg. Chim. Acta 2010, 363, 2496.
54. D. Oyama, K. Suzuki, T. Yamanaka, T. Tasuke, J. Coord. Chem. 2012, 65, 78.
55. J. M. Kelly, J. G. Vos, Angew. Chem. Int. Ed. Engl. 1982, 21, 628;
56. Angew. Chem. 1982, 94, 644.
57. Y. Kuramochi, M. Kamiya, H. Ishida, Inorg. Chem. 2014, 53, 3326;
58. A. Paul, D. Connolly, M. Schulz, M. T. Pryce, J. G. Vos, Inorg. Chem. 2012, 51, 1977.
59. Y. Kou, Y. Nabetani, D. Masui, T. Shimada, S. Takagi, H. Tachibana, H. Inoue, J. Am. Chem. Soc. 2014, 136, 6021;
60. M. D. Sampson, J. D. Froehlich, J. M. Smieja, E. E. Benson, I. D. Sharp, C. Kubiak, Energy Environ. Sci. 2013, 6, 3748;
61. J. Agarwal, E. Fujita, H. F. Schaefer, J. T. Muckerman, J. Am. Chem. Soc. 2012, 134, 5180.
62. G. A. Heath, L. J. Yellowlees, P. S. Braterman, J. Chem. Soc. Chem. Commun. 1981, 287;
63. J. V. Caspar, T. J. Meyer, Inorg. Chem. 1983, 22, 2444.
64. A. Neubauer, G. Grell, A. Friedrich, S. I. Bokarev, P. Schwarzbach, F. Gärtner, A.-E. Surkus, H. Junge, M. Beller, O. Kühn, S. Lochbrunner, J. Phys. Chem. Lett. 2014, 5, 1355;
65. Y. You, W. Nam, Chem. Soc. Rev. 2012, 41, 7061;
66. L. Flamigni, A. Barbieri, C. Sabatini, B. Ventura, F. Barigelletti, Top. Curr. Chem. 2007, 281, 143;
67. I. M. Dixon, J.-P. Collin, J.-P. Sauvage, L. Flamigni, S. Encinas, F. Barigelletti, Chem. Soc. Rev. 2000, 29, 385.
68. K. Maeda, K. Sekizawa, O. Ishitani, Chem. Commun. 2013, 49, 10127;
69. K. Sekizawa, K. Maeda, K. Domen, K. Koike, O. Ishitani, J. Am. Chem. Soc. 2013, 135, 4596.
70. M. S. Lowry, W. R. Hudson, R. A. Pascal, S. Bernhard, J. Am. Chem. Soc. 2004, 126, 14129.