Catalytic hydroxylation of benzene and toluene by an iron complex bearing a chelating di-pyridyl-di-NHC ligand

Chemical Communications

Volumn 50, Issue 78, 2014, Pages 11454-11457

  Raba, Andreas ^a   Cokoja, Mirza ^a   Herrmann, Wolfgang A ^a   Kühn, Fritz E ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; CARBENE; CRESOL; HYDROGEN PEROXIDE; IRON COMPLEX; LIGAND; OXYGEN; PHENOL; TOLUENE;

AQUEOUS SOLUTION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; FENTON REACTION; HIGH TEMPERATURE; HYDROXYLATION; LOW TEMPERATURE;

EID: 84908626834     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc02178a     Document Type: Article

References (32)

1. D. A. Alonso, C. Najera, I. M. Pastor, M. Yus, Chem. Eur. J., 2010, 16, 5274-5284
2. B. Lücke, K. V. Narayana, A. Martin, K. Jähnisch, Adv. Synth. Catal., 2004, 346, 1407-1424
3. J. H. Tyman, Synthetic and natural phenols, Elsevier, Amsterdam, 1996
4. R. J. Schmidt, Appl. Catal., A, 2005, 280, 89-103
5. B. Cornils, W. A. Herrmann, J. Catal., 2003, 216, 23-31
6. R. Ullrich, M. Hofrichter, Cell. Mol. Life Sci., 2007, 64, 271-293
7. P. R. Ortiz de Montellano, Cytochrome P-450 structure, mechanism, and biochemistry, Plenum Press, New York, 3 edn, 2010
8. A. Thibon, V. Jollet, C. Ribal, K. Senechal-David, L. Billon, A. B. Sorokin, F. Banse, Chem. - Eur. J., 2012, 18, 2715-2724
9. O. V. Makhlynets, E. V. Rybak-Akimova, Chem. - Eur. J., 2010, 16, 13995-14006
10. A. Thibon, J.-F. Bartoli, R. Guillot, J. Sainton, M. Martinho, D. Mansuy, F. Banse, J. Mol. Catal. A: Chem., 2008, 287, 115-120
11. S. P. de Visser, K. Oh, A.-R. Han, W. Nam, Inorg. Chem., 2007, 46, 4632-4641
12. S. Taktak, M. Flook, B. M. Foxman, L. Que Jr., E. V. Rybak-Akimova, Chem. Commun., 2005, 5301-5303
13. D. Mathieu, J. F. Bartoli, P. Battioni, D. Mansuy, Tetrahedron, 2004, 60, 3855-3862
14. V. Balland, D. Mathieu, N. Pons-Y-Moll, J. F. Bartoli, F. Banse, P. Battioni, J.-J. Girerd, D. Mansuy, J. Mol. Catal. A: Chem., 2004, 215, 81-87
15. D. Bianchi, R. Bortolo, R. Tassinari, M. Ricci, R. Vignola, Angew. Chem., Int. Ed., 2000, 39, 4321-4323
16. A. Raba, M. Cokoja, S. Ewald, K. Riener, E. Herdtweck, A. Pöthig, W. A. Herrmann, F. E. Kühn, Organometallics, 2012, 31, 2793-2800
17. W. Nam, Acc. Chem. Res., 2007, 40, 522-531
18. L. Que Jr., W. B. Tolman, Nature, 2008, 455, 333-340
19. A. R. McDonald, L. Que, Coord. Chem. Rev., 2013, 257, 414-428
20. H. Jacobsen, A. Correa, A. Poater, C. Costabile, L. Cavallo, Coord. Chem. Rev., 2009, 253, 687-703
21. T. Strassner, Top. Organomet. Chem., 2007, 22, 125-148
22. S. M. Podhajsky, M. S. Sigman, RSC Catal. Ser., 2011, 6, 345-365
23. J. W. Kück, A. Raba, I. I. E. Markovits, M. Cokoja, F. E. Kühn, ChemCatChem, 2014, 10.1002/cctc.201402063R1
24. C. Walling, R. A. Johnson, J. Am. Chem. Soc., 1975, 97, 363-367
25. S. Sahu, L. R. Widger, M. G. Quesne, S. P. de Visser, H. Matsumura, P. Moënne-Loccoz, M. A. Siegler, D. P. Goldberg, J. Am. Chem. Soc., 2013, 135, 10590-10593
26. A. Ansari, A. Kaushik, G. Rajaraman, J. Am. Chem. Soc., 2013, 135, 4235-4249
27. R. Latifi, L. Tahsini, W. Nam, S. P. de Visser, Phys. Chem. Chem. Phys., 2012, 14, 2518-2524
28. E. Olsson, A. Martinez, K. Teigen, V. R. Jensen, Chem. - Eur. J., 2011, 17, 3746-3758
29. M.-J. Kang, W. J. Song, A.-R. Han, Y. S. Choi, H. G. Jang, W. Nam, J. Org. Chem., 2007, 72, 6301-6304
30. T. Borowski, A. Bassan, P. E. M. Siegbahn, Inorg. Chem., 2004, 43, 3277-3291
31. Y.-R. Luo, Comprehensive handbook of chemical bond energies, CRC Press, Boca Raton, 2007
32. F. Gozzo, J. Mol. Catal. A: Chem., 2001, 171, 1-22