Versatile eco-friendly pickering emulsions based on substrate/native cyclodextrin complexes: A winning approach for solvent-free oxidations

ChemSusChem

Volumn 6, Issue 8, 2013, Pages 1533-1540

  Leclercq, Loïc ^a   Company, Roberto ^a   Mühlbauer, Andrea ^a   Mouret, Adrien ^a   Aubry, Jean Marie ^a   Nardello Rataj, Véronique ^a  

^a UNIV LILLE   (France)

Author keywords

cyclodextrins; nanoparticles; oxidation; Pickering emulsions; polyoxometalates

Indexed keywords

CATALYSTS; CATALYTIC OXIDATION; CYCLODEXTRINS; ENVIRONMENTAL PROTECTION; HYDROGEN PEROXIDE; NANOPARTICLES; OLEFINS; OXIDANTS; OXIDATION; PEROXIDES; SODIUM; SOLVENTS; THREE DIMENSIONAL;

COMPETITIVE RATES; CYCLODEXTRIN COMPLEXES; DISPERSED PHASE; GREEN OXIDANTS; INCLUSION COMPLEX; PICKERING EMULSIONS; POLYOXOMETALATES; SOLVENT-FREE OXIDATION;

COMPLEX NETWORKS;

CYCLODEXTRIN; EMULSION; HEPTANE; OXIDIZING AGENT; WATER; NANOPARTICLE;

CATALYSIS; CHEMISTRY; EMULSION; GREEN CHEMISTRY; OXIDATION REDUCTION REACTION; ARTICLE; OXIDATION; PICKERING EMULSIONS; POLYOXOMETALATES;

CATALYSIS; CYCLODEXTRINS; EMULSIONS; GREEN CHEMISTRY TECHNOLOGY; HEPTANES; OXIDANTS; OXIDATION-REDUCTION; WATER;

CYCLODEXTRINS; NANOPARTICLES; OXIDATION; PICKERING EMULSIONS; POLYOXOMETALATES;

EID: 84882312719     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.201300081     Document Type: Article

References (64)

1. P. T. Anastas, J. B. Zimmerman, Environ. Sci. Technol. 2003, 37, 94A-101A.
2. C. D. Frohning, C. W. Kohlpainter, in Applied Homogeneous Catalysis with Organometallic Compounds (Eds.:, B. Cornils, W. A. Herrmann,), Wiley-VCH, Weinheim, 1996, p. 29.
3. F. Cavani, G. Centi, S. Perathoner, F. Trifirò, Sustainable Industrial Chemistry, Wiley-VCH, Weinheim, 2009, p. 167.
4. C. Venturello, R. D'Aloisio, J. Org. Chem. 1988, 53, 1553-1557
5. Y. Ishii, K. Yamawaki, T. Ura, H. Yamada, T. Yoshida, M. Ogawa, J. Org. Chem. 1988, 53, 3587-3593
6. C. L. Hill, C. M. Prosser-McCartha, Coord. Chem. Rev. 1995, 143, 407-455
7. R. Neumann, Prog. Inorg. Chem. 1998, 47, 317-370
8. T. Sakamoto, C. Pac, Tetrahedron Lett. 2000, 41, 10009-10012
9. M. Klawonn, M. K. Tse, S. Bhor, C. Döbler, M. Beller, J. Mol. Catal. A: Chem. 2004, 218, 13-19
10. N. Mizuno, K. Yamaguchi, K. Kamata, Coord. Chem. Rev. 2005, 249, 1944-1956.
11. M. V. Vasylyev, R. Neumann, J. Am. Chem. Soc. 2004, 126, 884-890.
12. C. Jahier, L. Plault, S. Nlate, Isr. J. Chem. 2009, 49, 109-118.
13. A. Haimov, H. Cohen, R. Neumann, J. Am. Chem. Soc. 2004, 126, 11762-11763.
14. C. Venturello, E. Alneri, M. Ricci, J. Org. Chem. 1983, 48, 3831
15. C. Aubry, G. Chottard, N. Platzer, J.-M. Brégeault, R. Thouvenot, F. Chauveau, C. Huet, H. Ledon, Inorg. Chem. 1991, 30, 4409-4415
16. R. Neumann, A. M. Khenkin, J. Org. Chem. 1994, 59, 7577-7579
17. D. C. Duncan, R. C. Chambers, E. Hecht, C. L. Hill, J. Am. Chem. Soc. 1995, 117, 681-691
18. A. Lambert, P. Plucinski, I. V. Kozhevnikov, Chem. Commun. 2003, 714-715
19. Q. Wang, X. Zhang, L. Wang, Z. Mi, J. Mol. Catal. A: Chem. 2009, 309, 89-94.
20. L. Liu, C. Chen, X. Hu, T. Mohamood, W. Ma, J. Lin, J. Zhao, New J. Chem. 2008, 32, 283-289.
21. D. Attwood, A. T. Florence, Surfactant Systems: Their Chemistry, Pharmacy, and Biology, Chapman and Hall, London, 1983.
22. K. Shimada, Y. Ohe, T. Ohguni, K. Kawano, J. Ishii, T. Nakamura, Nippon Shokuhin Kogyo Gakkaishi 1991, 38, 16-20.
23. J. Szejtli, Chem. Rev. 1998, 98, 1743-1753.
24. K. Hashizaki, T. Kageyama, M. Inoue, H. Taguchi, H. Ueda, Y. Saito, Chem. Pharm. Bull. 2007, 55, 1620-1625
25. M. Inoue, K. Hashizaki, H. Taguchi, Y. Saito, Chem. Pharm. Bull. 2008, 56, 668-671
26. M. Inoue, K. Hashizaki, H. Taguchi, Y. Saito, Chem. Pharm. Bull. 2008, 56, 1335-1337
27. K. Hashizaki, T. Kageyama, M. Inoue, H. Taguchi, Y. Saito, J. Dispersion Sci. Technol. 2009, 30, 852-856
28. M. Inoue, K. Hashizaki, H. Taguchi, Y. Saito, J. Oleo Sci. 2009, 58, 85-90
29. M. Inoue, K. Hashizaki, H. Taguchi, Y. Saito, J. Dispersion Sci. Technol. 2010, 31, 1648-1651.
30. L. Davarpanah, F. Vahabzadeh, Starch/Staerke 2012, 64, 898-913.
31. S. Crossley, J. Faria, M. Shen, D. E. Resasco, Science 2010, 327, 68-72
32. J. Faria, M. Pilar Ruiz, D. E. Resasco, Adv. Synth. Catal. 2010, 352, 2359-2364
33. S. Drexler, J. Faria, M. Pilar Ruiz, J. H. Harwell, D. E. Resasco, Energy Fuels 2012, 26, 2231-2241
34. L. Leclercq, A. Mouret, A. Proust, V. Schmitt, P. Bauduin, J.-M. Aubry, V. Nardello-Rataj, Chem. Eur. J. 2012, 18, 14352-14358
35. H. Tan, P. Zhang, L. Wang, D. Yang, K. Zhou, Chem. Commun. 2011, 47, 11903-11905
36. Z. Wang, M. C. M. van Oers, F. P. J. T. Rutjes, J. C. M. van Hest, Angew. Chem. 2012, 124, 10904-10908
37. Angew. Chem. Int. Ed. 2012, 51, 10746-10750.
38. C. Yujuan, L. Runhua, Spectrochim. Acta, Part A 2009, 73, 713-718.
39. MOPAC2012, James J. P. Stewart, Stewart Computational Chemistry, Version 12.239W, http://www.openmopac.net.
40. C. Lemarchand, P. Couvreur, M. Besnard, D. Costantini, R. Gref, Pharm. Res. Pharmaceutical Res. 2003, 20, 1284-1292.
41. S. Arditty, C. P. Whitby, B. P. Binks, V. Schmitt, F. Leal-Calderon, Eur. Phys. J. 2003, 11, 273-281.
42. M. Munteanu, H. Ritter, in Biocatalysis in Polymer Chemistry (Ed.:, K. Loos,), Wiley-VCH, Weinheim, 2011, p. 398.
43. G. G. Allan, A. N. Neogi, J. Catal. 1970, 16, 197-203
44. X. Jian, A. S. Hay, J. Polym. Sci. Part A 1991, 29, 547-553
45. K. Kamata, K. Yamaguchi, N. Mizuno, Chem. Eur. J. 2004, 10, 4728-4734.
46. H.-J. Buschmann, E. Schollmeyer, J. Cosmet. Sci. 2002, 53, 185-191
47. J. L. Koontz, J. E. Marcy, S. F. O'Keefe, S. E. Duncan, J. Agric. Food Chem. 2009, 57, 1162-1171.
48. N. V. Maksimchuk, K. A. Kovalenko, S. S. Arzumanov, Y. A. Chesalov, M. S. Melgunov, A. G. Stepanov, V. P. Fedin, O. A. Kholdeeva, Inorg. Chem. 2010, 49, 2920-2930.
49. N. M. Gresley, W. P. Griffith, A. C. Laemmel, H. I. S. Nogueira, B. C. Parkin, J. Mol. Catal. A: Chem. 1997, 117, 185-198.
50. C. Song, X. Ma, Appl. Catal. B 2003, 41, 207-238.
51. K. Yazu, M. Makino, K. Ukegawa, Chem. Lett. 2004, 33, 1306-1307
52. J. M. Campos-Martin, M. C. Capel-Sanchez, J. L. G. Fierro, Green Chem. 2004, 6, 557-562
53. J. L. García-Gutiérrez, G. A. Fuentes, M. E. Hernández-Terán, F. Murrieta, J. Navarrete, F. Jiménez-Cruz, Appl. Catal. A 2006, 305, 15-20
54. R. Wang, G. Zhang, H. Zhao, Catal. Today 2010, 149, 117-121
55. W. Trakarnpruk, K. Rujiraworawut, Fuel Process. Technol. 2009, 90, 411-414.
56. H. Li, W. Zhu, J. Lu, X. Jiang, L. Gong, G. Zhu, Y. Yan, React. Kinet. Catal. Lett. 2009, 96, 165-173.
57. C. Li, Z. Jiang, J. Gao, Y. Yang, S. Wang, F. Tian, F. Sun, X. Sun, P. Ying, C. Han, Chem. Eur. J. 2004, 10, 2277-2280
58. C. Li, J. Gao, Z. Jiang, S. Wang, H. Lu, Y. Yang, F. Jing, Top. Catal. 2005, 35, 169-175.
59. X. Jiang, H. Li, W. Zhu, L. He, H. Shu, J. Lu, Fuel 2009, 88, 431-436.
60. M. Fressancourt-Collinet, B. Hong, L. Leclercq, P. Alsters, J.-M. Aubry, V. Nardello-Rataj, Adv. Synth. Catal. 2013, 355, 409-420.
61. P. Tundo, G. P. Romanelli, P. G. Vázquez, F. Aricò, Catal. Commun. 2010, 11, 1181-1184.
62. K. Yamawaki, N. Nishihara, T. Yoshida, T. Ura, H. Yamada, Y. Ishii, M. Ogawa, Synth. Commun. 1988, 18, 869-875.
63. G. D. Yadav, C. K. Mistry, J. Mol. Catal. A: Chem. 2001, 172, 135-149.
64. D. Sloboda-Rozner, P. L. Alsters, R. Neumann, J. Am. Chem. Soc. 2003, 125, 5280-5281.