Aerobic oxidative coupling of amines by carbon nitride photocatalysis with visible light

Angewandte Chemie - International Edition

Volumn 50, Issue 3, 2011, Pages 657-660

  Su, Fangzheng ^a   Mathew, Smitha C ^b   Möhlmann, Lennart ^b   Antonietti, Markus ^a   Wang, Xinchen ^a,c   Blechert, Siegfried ^b  

^a MAX PLANCK INSTITUTE OF COLLOIDS AND INTERFACES   (Germany)

^b TECHNISCHE UNIVERSITÄT BERLIN   (Germany)

^c FUZHOU UNIVERSITY   (China)

Author keywords

aerobic oxidative coupling; amines; carbon nitride; photochemistry; visible light

Indexed keywords

AEROBIC OXIDATIONS; BENZIMIDAZOLES; BENZOTHIAZOLES; BENZOXAZOLES; CASCADE REACTIONS; EFFICIENT SYNTHESIS; GRAPHITE CARBON; MESOPOROUS; ONE POT; OXIDATIVE COUPLINGS; PHOTO-CATALYTIC; PHOTOCHEMISTRY; VISIBLE LIGHT;

AMINES; PHOTOCATALYSIS; SYNTHESIS (CHEMICAL);

CARBON NITRIDE;

EID: 78651388766     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004365     Document Type: Article

References (36)

1. For example, see
2. N. Hoffmann, Chem. Rev. 2008, 108, 1052
3. D. A. Nicewicz, D. W. C. MacMillan, Science 2008, 322, 77.
4. S. Fukuzumi, Phys. Chem. Chem. Phys. 2008, 10, 2283.
5. A. Juris, V. Balzani, F. Barigelletti, S. Campagna, P. Belser, A. Vonzelewsky, Coord. Chem. Rev. 1988, 84, 85.
6. X. C. Wang, K. Maeda, A. Thomas, K. Takanabe, G. Xin, K. Domen, M. Antonietti, Nat. Mater. 2009, 8, 76.
7. J. S. Zhang, X. F. Chen, K. Takanabe, K. Maeda, K. Domen, J. D. Epping, X. Z. Fu, M. Antonietti, X. C. Wang, Angew. Chem. 2010, 122, 451
8. Angew. Chem. Int. Ed. 2010, 49, 441.
9. F. Z. Su, S. C. Mathew, G. Lipner, X. Z. Fu, M. Antonietti, S. Blechert, X. C. Wang, J. Am. Chem. Soc. 2010, 132, 16299.
10. J. Gawronski, N. Wascinska, J. Gajewy, Chem. Rev. 2008, 108, 5227.
11. M. V. George, K. S. Balachandran, Chem. Rev. 1975, 75, 491.
12. K. C. Nicolaou, C. J. N. Mathison, T. Montagnon, Angew. Chem. 2003, 115, 4211
13. Angew. Chem. Int. Ed. 2003, 42, 4077.
14. For example, see
15. K. Yamaguchi, N. Mizuno, Angew. Chem. 2003, 115, 1518
16. Angew. Chem. Int. Ed. 2003, 42, 1480
17. J. S. M. Samec, A. H. Ell, J.-E. Bäckvall, Chem. Eur. J. 2005, 11, 2327
18. B. L. Zhu, M. Lazar, B. G. Trewyn, R. J. Angelici, J. Catal. 2008, 260, 1.
19. For example, see
20. Y. X. Chen, L. F. Qian, W. Zhang, B. Han, Angew. Chem. 2008, 120, 9470
21. Angew. Chem. Int. Ed. 2008, 47, 9330
22. Y. Shiraishi, Y. Sugano, S. Tanaka, T. Hirai, Angew. Chem. 2010, 122, 1700
23. Angew. Chem. Int. Ed. 2010, 49, 1656.
24. N. Öcal, I. Erden, Tetrahedron Lett. 2001, 42, 4765
25. M. M. Heraci, L. Ranjbar, F. Derikcand, H. A. Oskooie, F. F. Bamoharram, J. Mol. Catal. A 2007, 265, 186.
26. H. C. Brown, Y. Okamoto, J. Am. Chem. Soc. 1958, 80, 4979.
27. For example, see
28. W. Schindler, H. Kisch, J. Photochem. Photobiol. A 1997, 103, 257
29. A. L. Linsebigler, G. Q. Lu, J. T. Yates, Chem. Rev. 1995, 95, 735
30. M. A. Fox, M. J. Chen, J. Am. Chem. Soc. 1983, 105, 4497.
31. M. Terashima, M. Ishii, Y. Kanaoka, Synthesis 1982, 484
32. G. Altenhoff, F. Glorius, Adv. Synth. Catal. 2004, 346, 1661
33. G. Evindar, R. A. Bartey, J. Org. Chem. 2006, 71, 1802.
34. M. Kidwai, V. Bansal, A. Saxena, S. Aerry, S. Mozumdar, Tetrahedron Lett. 2006, 47, 8049
35. N. Y. Ivanova, S. I. Sviridov, A. E. Stepanov, Tetrahedron Lett. 2006, 47, 8025
36. A. J. Blacker, M. M. Farah, M. I. Hall, S. P. Marsden, O. Saidi, J. M. J. Williams, Org. Lett. 2009, 11, 2039.