Carbon Dioxide to Methanol: The Aqueous Catalytic Way at Room Temperature

Chemistry - A European Journal

Volumn 22, Issue 44, 2016, Pages 15605-15608

  Sordakis, Katerina ^a   Tsurusaki, Akihiro ^b   Iguchi, Masayuki ^b   Kawanami, Hajime ^b   Himeda, Yuichiro ^b   Laurenczy, Gábor ^a  

^a EPFL   (Switzerland)

^b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

carbon dioxide; formic acid; homogeneous; hydrogenation; methanol

Indexed keywords

ADDITIVES; FORMIC ACID; HYDROGEN STORAGE; HYDROGENATION; METHANOL; ORGANIC CHEMICALS;

ACIDIC SOLUTIONS; CHEMICAL CARRIERS; DISPROPORTIONATIONS; HOMOGENEOUS; IRIDIUM CATALYST; REACTION TEMPERATURE; REDUCTION PRODUCTS;

CARBON DIOXIDE;

EID: 84991712958     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201603407     Document Type: Article

References (30)

1. M. Aresta, Carbon Dioxide as Chemical Feedstock, Wiley-VCH, Weinheim, 2010.
2. P. G. Jessop, in The Handbook of Homogeneous Hydrogenation (Eds.: J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, 2006, pp. 489–511.
3. G. A. Olah, G. K. S. Prakash, A. Goeppert, Beyond Oil and Gas: The Methanol Economy, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2009.
4. M. Nielsen, E. Alberico, W. Baumann, H.-J. Drexler, H. Junge, S. Gladiali, M. Beller, Nature 2013, 495, 85–89.
5. A. F. Dalebrook, W. Gan, M. Grasemann, S. Moret, G. Laurenczy, Chem. Commun. 2013, 49, 8735–8751.
6. K. Tominaga, Y. Sasaki, T. Watanabe, M. Saito, Bull. Chem. Soc. Jpn. 1995, 68, 2837–2842.
7. E. Balaraman, Y. Ben-David, D. Milstein, Angew. Chem. Int. Ed. 2011, 50, 11702–11705;
8. Angew. Chem. 2011, 123, 11906–11909.
9. E. Balaraman, C. Gunanathan, J. Zhang, L. J. W. Shimon, D. Milstein, Nat. Chem. 2011, 3, 609–614.
10. C. A. Huff, M. S. Sanford, J. Am. Chem. Soc. 2011, 133, 18122–18125.
11. Z. Han, L. Rong, J. Wu, L. Zhang, Z. Wang, K. Ding, Angew. Chem. Int. Ed. 2012, 51, 13041–13045;
12. Angew. Chem. 2012, 124, 13218–13222.
13. S. Wesselbaum, T. vom Stein, J. Klankermayer, W. Leitner, Angew. Chem. Int. Ed. 2012, 51, 7499–7502;
14. Angew. Chem. 2012, 124, 7617–7620.
15. S. Wesselbaum, V. Moha, M. Meuresch, S. Brosinski, K. M. Thenert, J. Kothe, T. vom Stein, U. Englert, M. Hölscher, J. Klankermayer, Chem. Sci. 2015, 6, 693–704.
16. N. M. Rezayee, C. A. Huff, M. S. Sanford, J. Am. Chem. Soc. 2015, 137, 1028–1031.
17. J. Kothandaraman, A. Goeppert, M. Czaun, G. A. Olah, G. K. S. Prakash, J. Am. Chem. Soc. 2016, 138, 778–781.
18. A. J. M. Miller, D. M. Heinekey, J. M. Mayer, K. I. Goldberg, Angew. Chem. Int. Ed. 2013, 52, 3981–3984;
19. Angew. Chem. 2013, 125, 4073–4076.
20. S. Savourey, G. Lefèvre, J.-C. Berthet, P. Thuéry, C. Genre, T. Cantat, Angew. Chem. Int. Ed. 2014, 53, 10466–10470;
21. Angew. Chem. 2014, 126, 10634–10638.
22. M. C. Neary, G. Parkin, Chem. Sci. 2015, 6, 1859–1865.
23. J. F. Hull, Y. Himeda, W.-H. Wang, B. Hashiguchi, R. Periana, D. J. Szalda, J. T. Muckerman, E. Fujita, Nat. Chem. 2012, 4, 383–388.
24. S. Moret, P. J. Dyson, G. Laurenczy, Nat. Commun. 2014, 5, 4017.
25. S. Moret, P. J. Dyson, G. Laurenczy, Dalton Trans. 2013, 42, 4353–4356.
26. W.-H. Wang, J. F. Hull, J. T. Muckerman, E. Fujita, T. Hirose, Y. Himeda, Chem. Eur. J. 2012, 18, 9397–9404.
27. A. Boddien, D. Mellmann, F. Gärtner, R. Jackstell, H. Junge, P. J. Dyson, G. Laurenczy, R. Ludwig, M. Beller, Science 2011, 333, 1733–1736.
28. R. H. Crabtree, M. Lavin, J. Chem. Soc. Chem. Commun. 1985, 1661–1662.
29. J. M. O′Connor, C. P. Casey, Chem. Rev. 1987, 87, 307–318.
30. T. Abura, S. Ogo, Y. Watanabe, S. Fukuzumi, J. Am. Chem. Soc. 2003, 125, 4149–4154.