Sonochemical syntheses of nano-sized dioxomolybdenum complexes: An efficient, selective and reusable heterogeneous nanocatalyst for oxidation of alkenes

Applied Catalysis A: General

Volumn 456, Issue , 2013, Pages 240-248

  Rayati, Saeed ^a   Abdolalian, Payam ^a  

^a K N TOOSI UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

Epoxidation; Heterogeneous nanocatalyst; Molybdenum; Olefins; Schiff base complexes; Ultrasonic irradiation

Indexed keywords

DIOXOMOLYBDENUM COMPLEXES; MILD REACTION CONDITIONS; NANO-CATALYST; SCHIFF BASE COMPLEXES; SONOCHEMICAL SYNTHESIS; TERT-BUTYLHYDROPEROXIDE; TRANSMISSION ELECTRON MICROSCOPY (TEM); ULTRASONIC IRRADIATION;

CATALYSTS; EPOXIDATION; FUNCTIONAL GROUPS; IRRADIATION; LIGANDS; MOLYBDENUM; MOLYBDENUM OXIDE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLEFINS; OXIDATION; SCANNING ELECTRON MICROSCOPY; SPECTROSCOPIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY;

CATALYTIC OXIDATION;

EID: 84876378825     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2013.03.003     Document Type: Article

References (63)

1. W. Adam, C.R. Saha-Moller, and P.A. Ganeshpure Chem. Rev. 101 2001 3499 3548
2. J. Rudolph, K.L. Reddy, J.P. Chiang, and K.B. Sharpless J. Am. Chem. Soc. 119 1997 6189 6190
3. C. Copéret, H. Adolfsson, and K.B. Sharpless Chem. Commun. 1997 1565 1566
4. D.E. de Vos, B.F. Sels, M. Reynaers, Y.V.S. Rao, and P.A. Jacobs Tetrahedron Lett. 39 1998 3221 3224
5. K. Sato, M. Aoki, M. Ogawa, T. Hashimoto, and R. Noyori J. Org. Chem. 61 1996 8310 8311
6. C.M.R. Low Ultrason. Sonochem. 2 1995 153 163
7. B.M. Adger, J.V. Barkley, S. Bergeron, M.W. Cappi, B.E. Flowerdew, M.P. Jackson, R. McCague, T.C. Nugent, and S.M. Rorberts J. Chem. Soc., Perkin Trans. 1 1997 3501 3508
8. D.Y. Kim, Y.J. Choi, H.Y. Park, C.U. Joung, K.O. Koh, J.Y. Mang, and K.Y. Jung Synth. Commun. 33 2003 435 443
9. V.K. Reddy, B. Haritha, and M. Yamashita Lett. Org. Chem. 2 2005 128
10. M.B. Andrus, and B.W. Poehlein Tetrahedron Lett. 41 2000 1013 1014
11. X.L. Geng, Z. Wang, X.Q. Li, and C. Zhang J. Org. Chem. 70 2005 9610 9613
12. J.V. Allen, K.H. Drauz, R.W. Flood, S.M. Roberts, and J. Skidmore Tetrahedron Lett. 40 1999 5417 5420
13. N. Hashimoto, and A. Kanda Org. Process Res. Dev. 6 2002 405
14. J.T. Groves, S.J. Crowley, and K.V. Shalyaev Proceedings of the 241st ACS National Meeting Las Vegas, NV J. Am. Chem. Soc. 1997 7 11
15. S. Rayati, S. Zakavi, M. Koliaei, A. Wojtczak, and A. Kozakiewicz Inorg. Chem. Commun. 13 2010 203 207
16. S. Rayati, and F. Ashouri Compt. Rend. Chim. 15 2012 679 687
17. S. Rayati, N. Rafiee, and A. Wojtczak Inorg. Chim. Acta 386 2012 27 35
18. S. Rayati, A. Ghaemi, and N. Sadeghzadeh Catal. Commun. 11 2010 792 796
19. F. Heshmatpour, S. Rayati, M.A. Hajiabbas, P. Abdolalian, and B. Neumüller Polyhedron 31 2012 443 450
20. S. Rayati, M. Koliaei, F. Ashouri, S. Mohebbi, A. Wojtczak, and A. Kozakiewicz Appl. Catal. A: Gen. 346 2008 65 71
21. S. Rayati, N. Sadeghzadeh, and H.R. Khavasi Inorg. Chem. Commun. 10 2007 1545 1548
22. S. Rayati, N. Torabi, A. Ghaemi, S. Mohebbi, A. Wojtczak, and A. Kozakiewicz Inorg. Chim. Acta 361 2008 1239 1245
23. B. Tamami, and S. Ghasemi Appl. Catal. A: Gen. 393 2011 242 250
24. A.J. Bonon, D. Mandelli, O.A. Kholdeeva, M.V. Barmatova, Y.N. Kozlov, and G.B. Shul'pin Appl. Catal. A: Gen. 365 2009 96 104
25. F. Marchetti, C. Pettinari, C. Di Nicola, R. Pettinari, A. Crispini, M. Crucianelli, and A. Di Giuseppe Appl. Catal. A: Gen. 378 2010 211 220
26. S. Rayati, S. Zakavi, S.H. Motlagh, V. Noroozi, M. Razmjoo, A. Wojtczak, and A. Kozakiewicz Polyhedron 27 2008 2285 2290
27. S. Zakavi, A.S. Ashtiani, and S. Rayati Polyhedron 29 2010 1492 1496
28. A. Rezaeifard, M. Jafarpour, S. Rayati, and R. Shariati Dyes Pigments 80 2009 80 85
29. D. Mohajer, and A. Rezaeifard Tetrahedron Lett. 43 2002 1881 1884
30. M. Bagherzadeh, R. Latifi, and L. Tahsini J. Mol. Catal. A: Chem. 260 2006 163 169
31. M. Herbert, F. Montilla, R. Moyano, A. Pastor, E. Álvarez, and A. Galindo Polyhedron 28 2009 3929 3934
32. Y. Ding, Q. Gao, G. Li, H. Zhang, J. Wang, L. Yan, and J. Suo J. Mol. Catal. A: Chem. 218 2004 161 170
33. E.P. Carreiro, A.J. Burke, M.J.M. Curto, and A.J.R. Teixeira J. Mol. Catal. A: Chem. 17 2004 69 72
34. F.L. Braghiroli, J.C.S. Barboza, and A.A. Serra Ultrason. Sonochem. 13 2006 443 445
35. H. Salavati, S. Tangestaninejad, M. Moghadam, V. Mirkhani, and I. Mohammadpoor-Baltork Ultrason. Sonochem. 17 2010 145 152
36. H. Jin, H. Zhao, F. Zhao, S. Li, W. Liu, G. Zhou, K. Tao, and T. Hou Ultrason. Sonochem. 16 2009 304 307
37. G. Chatel, C. Goux-Henry, N. Kardos, J. Suptil, B. Andrioletti, and M. Draye Ultrason. Sonochem. 19 2012 390 394
38. A. Askarinejad, M. Bagherzadeh, and A. Morsali Appl. Surf. Sci. 256 2010 6678 6682
39. X.-H. Lu, Q.-H. Xia, D. Zhou, S.-Y. Fang, A.-L. Chen, and Y.-L. Dong Catal. Commun. 11 2009 106 109
40. S. Rayati, S. Zakavi, P. Jafarzadeh, O. Sadeghi, and M.M. Amini J. Porphyrins Phthalocyanines 16 2011 260 266
41. C.-J. Liu, W.-Y. Yu, S.-G. Li, and C.-M. Che J. Org. Chem. 63 1998 7364 7369
42. X.-Q. Yu, J.-S. Huang, W.-Y. Yu, and C.-M. Che J. Am. Chem. Soc. 122 2000 5337 5342
43. Z. Li, C.-G. Xia, and X.-M. Zhang J. Mol. Catal. A: Chem. 185 2002 47 56
44. H. Yang, Z. Ma, Y. Qing, G. Xie, J. Gao, L. Xhang, J. Gao, and L. du Appl. Catal. A: Gen. 382 2010 312 321
45. A.S. Amarasekara, I. McNeal, J. Murillo, D. Green, and A. Jennings Catal. Commun. 9 2008 2437 2440
46. B. Neppolian, E. Celik, M. Anpo, and H. Choi Catal. Lett. 125 2008 183 191
47. T. Mason, and D. Petersn Pract. Sonochem. 2 2002 17
48. S.K. Maiti, K.M. AbdulMalik, and R. Bhattacharyya Inorg. Chem. Commun. 7 2004 823 828
49. S. Gago, P. Neves, B. Monteiro, M. Pessêgo, A.D. Lopes, A.A. Valente, F.A. Almeida Paz, M. Pillinger, J. Moreira, C.M. Silva, and I.S. Gonçalves Eur. J. Inorg. Chem. 2009 4528 4537
50. P. Neves, S. Gago, C.C.L. Pereira, S. Figueiredo, A. Lemos, A.D. Lopes, I.S. Goncalves, M. Pillinger, C.M. Silva, and A.A. Valente Catal. Lett. 132 2009 94 103
51. F.-L. Chai, H.-L. Su, X.-Y. Wang, and J.-C. Tao Inorg. Chim. Acta 362 2009 3840 3844
52. A. Syanal, and D. Kumar Indian J. Chem. 21A 1982 534
53. Y. Sui, X. Zeng, X. Fang, X. Fu, Y. Xiao, L. Chen, M. Li, and S. Cheng J. Mol. Catal. A: Chem. 270 2007 61 67
54. J. Topich Inorg. Chem. 20 1981 3704
55. F.E. Kuhn, M. Groarke, E. Bencze, E. Herdtweck, A. Prazeres, A.M. Santos, M.J. Calhorda, C.C. Romao, I.S. Goncalves, A.D. Lopes, and M. Pillinger Chem. Eur. J. 8 2002 2370 2383
56. M. Minelli, J.H. Enemark, R.T.C. Brownlee, M.J. O'Connor, and A.G. Wedd Coord. Chem. Rev. 68 1985 169 278
57. J.M. Sobczak, and J.J. Zíołkowski Appl. Catal. A: Gen. 248 2003 261 268
58. J.M. Sobczak, and J.J. Ziolkowski J. Mol. Catal. 13 1981 11 42
59. Z. Hu, X. Fu, and Y. Li Inorg. Chem. Commun. 14 2011 497 501
60. M. Masteri-Farahani J. Mol. Catal. A: Chem. 316 2010 45 51
61. Y. Li, X. Fu, B. Gong, X. Zou, X. Tu, and J. Chen J. Mol. Catal. A: Chem. 322 2010 55 62
62. M. Masteri-Farahani, F. Farzaneh, and M. Ghandi J. Mol. Catal. A: Chem. 248 2006 53 60
63. M. Moghadam, V. Mirkhani, S. Tangestaninejad, I. Mohammadpoor-Baltork, and M.M. Javadi Polyhedron 29 2010 648 654