The catalytic efficiency of Fe-porphyrins supported on multi-walled carbon nanotubes in the heterogeneous oxidation of hydrocarbons and sulfides in water

Catalysis Science and Technology

Volumn 4, Issue 7, 2014, Pages 1960-1969

  Rezaeifard, Abdolreza ^a   Jafarpour, Maasoumeh ^a  

^a UNIVERSITY OF BIRJAND   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

ATOMIC EMISSION SPECTROSCOPY; BIOMIMETICS; CATALYST SELECTIVITY; CATALYTIC OXIDATION; CHLORINE COMPOUNDS; HYDROCARBONS; INDUCTIVELY COUPLED PLASMA; IRON COMPOUNDS; KETONES; OXIDATION; PORPHYRINS; SCANNING ELECTRON MICROSCOPY; THERMOGRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET VISIBLE SPECTROSCOPY; X RAY DIFFRACTION;

BIOMIMETIC CATALYSTS; CATALYTIC EFFICIENCIES; HETEROGENEOUS CATALYST; HETEROGENEOUS OXIDATION; HYDROXYL FUNCTIONALITY; INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION SPECTROSCOPY; POWDER X RAY DIFFRACTION; SATURATED HYDROCARBONS;

LOADING;

EID: 84897998539     PISSN: 20444753     EISSN: 20444761     Source Type: Journal    
DOI: 10.1039/c3cy00554b     Document Type: Article

References (71)

1. B. P. S. Chauhan, Hybrid Nanomaterials: Synthesis, Characterization and Applications, John Wiley & Son, New Jersey, 2011
2. E. Ruiz-Hitzky, K. Ariga and Y. Lvov, Bio-inorganic Hybrid Nanomaterials: Strategies, Synthesis, Characterization and Applications, VCH, Weinheim, Germany, 2008
3. M. Beyrhouty A. B. Sorokin S. Daniele L. G. Hubert-Pfalzgraf New J. Chem. 2005 29 1245 1248
4. D. Ren Z. Guo F. Du J. Zheng Y. Chen J. Nanosci. Nanotechnol. 2007 7 1539 1545
5. M. Monthioux, Carbon Meta-Nanotubes: Synthesis, Properties and Applications, Wiley and Sons, 2012
6. N. Martin and J.-F. Nierengarten, Supramolecular Chemistry of Fullerenes and Carbon Nanotubes, VCH, Weinheim, Germany, 2012
7. B. Wu Y. Kuang X. Zhang J. Chen Nano Today 2011 6 75 90
8. C. N. R. Rao A. Govindaraj Acc. Chem. Res. 2002 35 998 1007
9. C. H. Li K. F. Yao J. Liang Carbon 2003 41 858 860
10. D. E. De Vos, I. F. J. Vankelecom and P. A. Jacobs, Chiral catalyst immobilization and recycling, VCH, Weinheim, Germany, 2000
11. V. A. Likholobov and B. L. Moroz, in Handbook of Heterogeneous Catalysis, ed., G. Ertl, H. Knozzinger, and, J. Weitkamp, VCH, Weinheim, Germany, 1997, vol. 5, pp. 2231-2244
12. P. Tribolet L. Kiwi-Minsker Catal. Today 2005 102-103 15 22
13. H. Tang J. H. Chen Z. P. Huang S. Z. Yao Carbon 2004 42 191 197
14. P. Serp M. Corrias P. Kalck Appl. Catal., A 2003 253 337 358
15. F. Davis and S. Higson, Macrocycles: Construction, Chemistry and Nanotechnology Applications, Wiley and Sons, 2011
16. B. Meunier, Biomimetic Oxidations Catalyzed by Transition Metal Complexes, Imperial College Press, 2000
17. D. J. Cole-Hamilton Science 2003 299 1702 1706
18. N. E. Leadbeater M. Marco Chem. Rev. 2002 102 3217 3273
19. Q.-H. Fan Y.-M. Li A. S. C. Chan Chem. Rev. 2002 102 3385 3466
20. C. E. Song S.-G. Lee Chem. Rev. 2002 102 3495 3524
21. A. Akelah D. C. Sherrington Chem. Rev. 1981 81 557 587
22. D. C. Bailey S. H. Langer Chem. Rev. 1981 81 109 148
23. C. A. McNamara M. J. Dixon M. Bradley Chem. Rev. 2002 102 3275 3299
24. E. Brule Y. R. De Miguel Org. Biomol. Chem. 2006 4 599 609
25. J. L. Zhang Y. L. Liuab C. M. Che Chem. Commun. 2002 2906 2907
26. Z. Li C.-G. Xia X.-M. Zhang J. Mol. Catal. A: Chem. 2002 185 47 56
27. P. Dixneuf and V. Cadierno, Metal-Catalyzed Reactions in Water, VCH, New York, 2013
28. U. M. Lindstrom, Organic Reactions in Water: Principles, Strategies and Applications, VCH, 2007
29. R. Ballini, Eco-Friendly Synthesis of Fine Chemicals, RSC, 2009
30. R. A. Sheldon, I. Arends and U. Hanefeld, Green Chemistry and Catalysis, VCH, Weinheim, Germany, 2007
31. K. Mikami, Green Reaction Media in Organic Synthesis, Blackwell, 2005
32. C. J. Li and T. K. Chan, Organic Reactions in Aqueous Media, John Wiley & Son, New York, 1997
33. P. A. Grieco, Organic Synthesis in Water, Blackie Academic and Professional, London, 1998
34. A. Lubineau Chem. Ind. 1996 4 123 126
35. A. Lubineau and J. Auge, Topics in Current Chemistry, vol. 206, Springer-Verlag, Berlin, 1999
36. A. Rezaeifard M. Jafarpour A. Naeimi S. Kaafi Catal. Commun. 2011 12 761 765
37. A. Rezaeifard M. Jafarpour A. Naeimi Catal. Commun. 2011 16 240 244
38. A. Rezaeifard M. Jafarpour A. Naeimi M. Salimi Inorg. Chem. Commun. 2012 15 230 234
39. A. Rezaeifard M. Jafarpour A. Naeimi K. Mohammadi J. Mol. Catal. A: Chem. 2012 357 141 147
40. A. Rezaeifard M. Jafarpour P. Farshid A. Naeimi Eur. J. Inorg. Chem. 2012 5515 5524
41. A. Rezaeifard M. Jafarpour A. Naeimi R. Haddad Green Chem. 2012 14 3386 3394
42. A. Rezaeifard V. Soltani M. Jafarpour Eur. J. Inorg. Chem. 2013 2657 2664
43. A. Rezaeifard R. Haddad M. Jafarpour M. Hakimi J. Am. Chem. Soc. 2013 135 10036 10039
44. M. Jafarpour M. Gharamaninejad A. Rezaeifard RSC Adv. 2014 4 1601 1608
45. A. Rezaeifard P. Farshid M. Jafarpour Gh. Kardan Moghaddam RSC Adv. 2014 4 9189 9196
46. A. Rezaeifard R. Haddard M. Jafarpour M. Hakimi ACS Sustainable Chem. Eng. 2014 2 942 950
47. M. S. P. Shaffer X. Fan A. H. Windle Carbon 1998 36 1603 1612
48. H. Sharghi M. H. Beyzavi A. Safavi M. M. Doroodmand R. Khalifeh Adv. Synth. Catal. 2009 351 2391 2410
49. A. V. Udaltsov M. Tosaka G. Kaupp J. Mol. Struct. 2003 660 15 23
50. M. Endo K. Takeuchi T. Hiraoka T. Furuta T. Kasai X. Sun C.-H. Kiang M. S. Dresselhaus J. Phys. Chem. Solids 1997 58 1707 1712
51. P. Saini V. Choudhary B. P. Singh R. B. Mathur S. K. Dhawan Mater. Chem. Phys. 2009 113 919 926
52. H. Grebel Z. Iqbal A. Lan Chem. Phys. Lett. 2001 348 203 208
53. A. M. Rao A. Jario M. A. Pimenta M. S. Dantas R. Saito G. Dresswlhaus M. S. Dresselhaus Phys. Rev. Lett. 2000 84 1820 1823
54. T. Natsuki1 G. J. H. Melvin Q.-Q. Ni J. Mater. Sci. Res. 2013 2 1 11
55. N. Z. Mamardashivili O. A. Golubchikov Russ. Chem. Rev. 2001 70 577 606
56. H. Sharghi M. H. Beyzavi M. M. Doroodmand Eur. J. Org. Chem. 2008 4126 4138
57. T. Kitagawa Y. Mizutani Coord. Chem. Rev. 1994 135-136 685
58. H.-Z. Zhao Y.-Y. Chang C. Liu J. Solid State Electrochem. 2013 17 1657 1664
59. B. Tyagi U. Sharma R. V. Jasra Appl. Catal., A 2011 408 171 177
60. X. Meng K. Lin J. Sun M. Yang D. Jiang F.-S. Xiao Catal. Lett. 2001 71 241 244
61. Y. Ding W. Zhao H. Hua B. Ma Green Chem. 2008 10 910 913
62. E. G. Ankudey H. F. Olivo T. L. Peeples Green Chem. 2006 8 923 926
63. F. Bruyneel C. Letondor B. Bastürk A. Gualandi A. Pordea H. Stoeckli-Evans R. Neier Adv. Synth. Catal. 2012 354 428 440
64. F. Rajabi S. Naserian A. Primo R. Luque Adv. Synth. Catal. 2011 353 2060 2066
65. L. Xu J. Cheng M. L. Trudel J. Org. Chem. 2003 68 5388
66. J. M. Samanen E. Brandeis J. Org. Chem. 1988 53 561 569
67. M. H. Ali G. J. Bohnert Synth. Commun. 1998 28 2983 2998
68. A. D. Adler F. R. Longo J. D. Finarelli J. Goldmacher J. Assour L. Korsakoff J. Org. Chem. 1967 32 476
69. D. Ostovic T. C. Bruice J. Am. Chem. Soc. 1989 111 6511 6517
70. P. K. Kumar P. Bhyrappa B. Varghese Tetrahedron Lett. 2003 44 4849 4851
71. B. R. Travis B. P. Ciaramitaro B. Borhan Eur. J. Org. Chem. 2002 3429 34348