Aerobic Oxidation of Thiols Catalyzed by Copper Nanoparticles Supported on Diamond Nanoparticles

ChemCatChem

Volumn 5, Issue 1, 2013, Pages 241-246

  Dhakshinamoorthy, Amarajothi ^a   Navalon, Sergio ^a   Sempere, David ^a   Alvaro, Mercedes ^a   Garcia, Hermenegildo ^a  

^a INSTITUTO DE TECNOLOGÍA QUÍMICA   (Spain)

Author keywords

Aerobic oxidation; Copper; Diamond; Nanoparticles; Thiophenol

Indexed keywords

AEROBIC OXIDATIONS; ALIPHATIC THIOLS; ANNEALING PROCESS; AROMATIC THIOL; AU CATALYSTS; CARBOXYLIC ACID GROUPS; COPPER NANOPARTICLES; CU NANOPARTICLES; DIAMOND NANOPARTICLES; FENTON TREATMENT; SOLID SUPPORTS; THIOPHENOLS; XRD;

CARBOXYLIC ACIDS; CATALYST ACTIVITY; COPPER; HYDROGEN; NANOPARTICLES; OXIDATION; PHOTOELECTRONS; PURIFICATION; X RAY PHOTOELECTRON SPECTROSCOPY;

DIAMONDS;

EID: 84871665199     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201200569     Document Type: Article

References (29)

1. E. Zysman-Colman, D. N. Harpp, J. Org. Chem. 2005, 70, 5964.
2. R. J. Cremlyn in An Introduction to Organosulfur Chemistry, Wiley, New York, 1996.
3. G. H. Whitham in Organosulfur Chemistry, Oxford University Press, Oxford, 1995.
4. S. Ghammamy, M. Tajbakhsh, J. Sulfur Chem. 2005, 26, 145.
5. H. Karami, M. Montazerozohori, M. H. Habibi, J. Chem. Res. 2006, 8, 490.
6. L. Bischoff, C. David, L. Martin, H. Meudal, B.-P. Roques, M.-C. Fournie-Zaluski, J. Org. Chem. 1997, 62, 4848.
7. F. Hosseinpoor, H. Golchoubian, Catal. Lett. 2006, 111, 165.
8. N. A. Noureldin, M. Caldwell, J. Hendry, D. G. Lee, Synthesis 1998, 1587.
9. M. H. Ali, M. McDermott, Tetrahedron Lett. 2002, 43, 6271.
10. A. R. Ramesha, S. Chandrasekaran, J. Org. Chem. 1994, 59, 1354.
11. D. K. Y. Tan, J. W. Kee, W. Y. Fan, Organometallics 2010, 29, 4459.
12. K. Y. D. Tan, G. F. Teng, W. Y. Fan, Organometallics 2011, 30, 4136.
13. A. R. Hajipour, S. E. Mallakpour, H. Adibi, J. Org. Chem. 2002, 67, 8666.
14. H. Golchoubian, F. Hosseinpoor, Catal. Commun. 2007, 8, 697.
15. S. M. S. Chauhan, A. Kumar, K. A. Srinivas, Chem. Commun. 2003, 2348.
16. K. Tanaka, K. Ajiki, Tetrahedron Lett. 2004, 45, 25.
17. A. Dhakshinamoorthy, M. Alvaro, H. Garcia, Chem. Commun. 2010, 46, 6476.
18. D. R. Dreyer, H.-P. Jia, A. D. Todd, J. Geng, C. W. Bielawski, Org. Biomol. Chem. 2011, 9, 7292.
19. A. Corma, T. Rodenas, M. J. Sabater, Chem. Sci. 2012, 3, 398.
20. S. Navalon, R. Martin, M. Alvaro, H. Garcia, Angew. Chem. 2010, 122, 8581; Angew. Chem. Int. Ed. 2010, 49, 8403.
21. S. Osswald, G. Yushin, V. Mochalin, S. Kucheyev, Y. Gogotsi, J. Am. Chem. Soc. 2006, 128, 11635.
22. K. J. Carroll, J. U. Reveles, M. D. Shultz, S. N. Khanna, E. E. Carpenter, J. Phys. Chem. C 2011, 115, 2656.
23. R. J. Joseyphus, K. Shinoda, D. Kodama, B. Jeyadevan, Mater. Chem. Phys. 2010, 123, 487.
24. R. Martin, S. Navalon, J. J. Delgado, J. J. Calvino, M. Alvaro, H. Garcia, Chem. Eur. J. 2011, 17, 9494-9502.
25. C. M. Chanquía, L. Andrini, J. D. Fernández, M. E. Crivello, F. G. Requejo, E. R. Herrero, G. A. Eimer, J. Phys. Chem. C 2010, 114, 12221.
26. H. Lei, Y. Tang, J. Li, J. Luo, Appl. Phys. Lett. 2007, 91, 113.
27. K. Yoshida, C. Gonzalez-Arellano, R. Luque, P. L. Gai, Appl. Catal. A 2010, 379, 38.
28. T.-Y. Dong, H. H. Wua, C. Huang, J. M. Song, I. G. Chen, T. H. Kao, Appl. Surf. Sci. 2009, 255, 3891.
29. P. Gamez, I. W. C. E. Arends, J. Reedijk, R. A. Sheldon, Chem. Commun. 2003, 2414.