Article
Atashin and Malakooti
M. J. Mol. Catal. A: Chem. 2013, 372, 167.
Schematic of proposed mechanism for the
oxidation of alcohols
Scheme 3
12. Zhang, G.; Wang, Y.; Wen, X.; Ding, C.; Li, Y. Chem.
Commun. 2012, 48, 2979.
13. Wang, H.; Wang, J. G.; Shen, Z. R.; Liu, Y. P.; Ding, D. T.;
Chen, T. H. J. Catal. 2010, 275, 140.
14. Yang, H.; Chong, Y.; Li, X.; Ge, H.; Fan, W.; Wang, J. J. Ma-
ter. Chem. 2012, 22, 9069.
15. Karimi, B.; Elhamifar, D.; Clark, J. H.; Hunt, A. J. Org.
Biomol. Chem. 2011, 9, 7420.
16. Yang, H.; Han, X.; Ma, Z.; Wang, R.; Liu, J.; Jia, X. Green
Chem. 2010, 12, 441.
17. Witham, C. A.; Huang, W.; Tsung, C. K.; Kuhn, J. N.;
Somorjai, G. A.; Toste, F. D. Nat. Chem. 2010, 2, 36.
18. Konya, Z.; Molnar, E.; Tasi, G.; Niesz, K.; Somorjai, G. A.;
Kiricsi, I. Catal. Lett. 2007, 113, 19.
19. Yang, C. M.; Sheu, H. S.; Chao, K. J. Adv. Funct. Mater.
2002, 12, 143.
tion of a variety of alcohols in two different conditions.
High conversion, relatively short reaction times and good
reusability are advantages of our work.
20. Raja, R.; Sankar, G.; Hermann, S.; Shephard, D. S.; Bromley,
S.; Thomas, J. M.; Johnson, B. F. G. Chem. Commun. 1999,
16, 1571.
21. Han, Y. J.; Kim, J. M.; Stucky, G. D. Chem. Mater. 2000, 12,
2068.
ACKNOWLEDGEMENTS
22. White, R. J.; Luque, R.; Budarin, V. L.; Clark, J. H.;
Macquarrie, D. J. Chem. Soc. Rev. 2009, 38, 481.
23. Liu, Q.; Bauer, J. C.; Schaak, R. E.; Lunsford, J. H. Angew.
Chem. Int. Ed. 2008, 47, 6221.
Authors are thankful to University of Birjand Re-
search Council for the funding of this study. We also grate-
fully acknowledge Dr. R. Hosseinabadi and Dr. E. Ghiamati
(University of Birjand) for their useful consults
24. Jana, S.; Dutta, B.; Bera, R.; Koner, S. Inorg. Chem. 2008,
47, 5512.
REFERENCES
25. Wang, X.; Wu, G.; Wei, W.; Sun, Y. Catal. Lett. 2010, 36, 96.
26. Lim, M. H.; Stein, A. Chem. Mater. 1999, 11, 3285.
27. Hernandez-Pineda, J.; Del-Rio, J. M.; Carreto, E.; Terres, E.;
Montoya, J. A.; Zuniga-Gonzaleza, M. D. J.; Morgado, J. J.
Alloys Compd. 2009, 481, 526.
1. Stahl, S. S. Angew. Chem. Int. Ed. 2004, 43, 3400.
2. Brink, G. J.; Arends, I. W. C. E.; Sheldon, R. A. Science
2000, 287, 1636.
3. Shi, Z.; Zhang, C.; Tang, C.; Jiao, N. Chem. Soc. Rev. 2012,
41, 3381.
28. Feng, Y.; Li, L.; Li, Y.; Zhao, W.; Gu, J.; Shi, J. J. Mol. Catal.
A: Chem. 2010, 322, 50.
4. Mallat, T.; Baiker, A. Chem. Rev. 2004, 104, 3037.
5. Parmeggiani, C.; Cardona, F. Green Chem. 2012, 14, 14547.
6. Zhao, D.; Feng, J.; Huo, Q.; Melosh, N.; Fredrickson, G. H.;
Chmelka, B. F.; Stucky, G. D. Science 1998, 279, 548.
7. Karimi, B.; Abedi, S.; Clark, J. H.; Budarin, V. Angew.
Chem. Int. Ed. 2006, 45, 4776.
29. Zhao, X. G.; Shi, J. L.; Hu, B.; Zhang, L. X.; Hua, Z. L. Ma-
ter. Lett. 2004, 58, 2152.
30. Chen, X.; Hirtz, M.; Rogach, A. L.; Talapin, D. V.; Fuchs,
H.; Chi, L. Nano. Lett. 2007, 11, 3483.
31. Zhao, D.; Sun, J.; Li, Q.; Stucky, G. D. Chem. Mater. 2000,
12, 275.
8. Chen, J.; Zhang, Q.; Wang, Y.; Wan, H. Adv. Synth. Catal.
2008, 350, 453.
32. Layek, K.; Maheswaran, H.; Arundhathi, R.; Lakshmi-
Kantam, M.; Bhargavab, S. K. Adv. Synth. Catal. 2011, 353,
606.
9. Ma, Z.; Yang, H.; Qin, Y.; Hao, Y.; Li, G. J. Mol. Catal. A:
Chem. 2010, 331, 78.
10. Hou, Y.; Ji, X.; Liu, G.; Tang, J.; Zheng, J.; Liu,Y.; Zhang,
W.; Jia, M. Catal. Commun. 2009, 10, 1459.
11. Alizadeh, A.; Khodaei, M. M.; Kordestania, D.; Beygzadeh,
33. Mori, K.; Hara, T.; Mizugaki, Tomoo.; Ebitani, K.; Kaneda,
K. J. Am.Chem. Soc. 2004, 126, 10657.
1044
© 2014 The Chemical Society Located in Taipei & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim J. Chin. Chem. Soc. 2014, 61, 1039-1044