A green reduction of aromatic nitro compounds to aromatic amines over a novel Ni/SiO2 catalyst passivated with a gas mixture

Catalysis Letters

Volumn 124, Issue 3-4, 2008, Pages 268-276

  Zheng, Yunfeng ^a   Ma, Kun ^a   Wang, Huanling ^a   Sun, Xun ^a   Jiang, Jian ^a   Wang, Chaofeng ^a   Li, Rong ^a   Ma, Jiantai ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

Aromatic amines; Aromatic nitro compounds; Catalytic hydrogenation; Ni SiO2; Passivated

Indexed keywords

AMINES; ARSENIC COMPOUNDS; CHLORINE COMPOUNDS; ORGANIC COMPOUNDS;

AROMATIC AMINES; AROMATIC NITRO COMPOUNDS; CATALYTIC HYDROGENATION; NI/SIO2; PASSIVATED; PRACTICAL METHODS;

AROMATIC COMPOUNDS;

EID: 49749104284     PISSN: 1011372X     EISSN: 1572879X     Source Type: Journal    
DOI: 10.1007/s10562-008-9452-2     Document Type: Article

References (59)

1. Booth G (2002) Ullmanns encyclopedia of industrial chemistry. Wiley-VCH Verlag, Weinheim
2. (a) Figueras F, Coq B (2001) J Mol Catal A: Chem 173:117-134;
3. (b) Figueras F, Coq B (2001) J Mol Catal A: Chem 173:223-230
4. Mitchell SC, Waring RH (2000) Ullmanns encyclopedia of industrial chemistry. Wiley-VCH Verlag, Weinheim
5. Bechamp AJ (1854) Anal Chim Phys 42:140
6. Lakshmi Kantam M, Bandyopadhyay T, Rahman A, Mahender Reddy N, Choudary BM (1998) J Mol Catal A: Chem 133:293-295
7. Xu S, Xi X, Shi J, Cao S (2000) J Mol Catal A: Chem 160:287-292
8. Chen Y, Qiu J, Wang X, Xiu J (2006) J Catal 242:227-230
9. Du Y, Chen H, Chen R, Xu N (2004) Appl Catal A: Gen 277:259-264
10. Joseph T, Vijay Kumar K, Ramaswamy AV, Halligudi SB (2007) Catal Commun 8:629-634
11. (a) Cardenas-Lizana F, Gomez-Quero S, Keane MA (2008) Catal Commun 9:475-481.
12. (b) Cardenas-Lizana F, Gomez-Quero S, Keane MA (2008) Appl Catal A: Gen 334:199-206
13. Bovkun TT, Grayevsky M, Sasson Y, Bluma J (2007) J Mol Catal A: Chem 270:171-176
14. Shen J-H, Chen Y-W (2007) J Mol Catal A: Chem 273:265-276
15. Basu B, Das S, Das P, Nanda AK (2005) Tetrahedron Lett 46:8591-8593
16. Murthy KV, Patterson PM, Jacobs G, Davis BH, Keane MA (2004) J Catal 223:74-85
17. Xi X, Liu Y, Shi J, Cao S (2003) J Mol Catal A: Chem 192:1-7
18. Keum Y-S, Li QX (2004) Chemosphere 54:255-263
19. Corma A, Serna P (2006) Science 313:332
20. Corma A, Concepcion P, Serna P (2007) Angew Chem Int Ed 46:7266 -7269
21. Raja R, Golovko VB, Thomas JM, Berenguer-Murcia A, Zhou W, Xie S, Johnson BFG (2005) Chem Commun 2026-2028
22. He D, Shi H, Wu Y, Xu B-Q (2007) Green Chem 9:849-851
23. Kulkarni AS, Jayaram RV (2003) Appl Catal A: Gen 252:225-230
24. Kulkarni AS, Jayaram RV (2004) J Mol Catal A: Chem 223:107-110
25. Mohapatra SK, Sonavane SU, Jayaram RV, Selvam P (2002) Tetrahedron Lett 43(47): 8527-8529
26. Mohapatra SK, Sonavane SU, Jayaram RV, Selvam P (2002) Org Lett 4(24): 4297-4300
27. Benz M, Prins R (1999) Appl Catal A: Gen 183:325-333
28. Abiraj K, Srinivasa GR, Gowda DC (2005) Aust J Chem 58(2):149-151
29. Abiraj K, Srinivasa GR, Gowda DC (2005) Synth Commun 35(2):223-230
30. Jyothi TM, Rajagopal R, Sreekumar K, Talawar MB, Sugunanb S, Rao BS (1999) J Chem Res (S):674-675
31. Joshi MV, Mukesh D (1997) J Catal 168:273-277
32. Mdleleni MM, Rinker RG, Ford PC (2003) J Mol Catal A: Chem 204-205:125-131
33. Nomura K (1995) J Mol Catal A: Chem 95:203-210
34. Liu X, Lu S (2004) J Mol Catal A: Chem 212:127-130
35. Basu MK, Becker FF, Banik BK (2000) Tetrahedron Lett 41:5603-5606
36. Lauwiner M, Rys P, Wissmann J (1998) Appl Catal A: Gel 172:141-148
37. Pogorelić I, Filipan-Litvić M, Merkaš S, Ljubić G, Cepanec I, Litvić M (2007) J Mol Catal A: Chem 274:202-207
38. Gowda S, Channe Gowda D (2002) Tetrahedron 58:2211-2213
39. Khan FA, Dash J, Sudheer Ch, Gupta RK (2003) Tetrahedron Lett 44:7783-7787
40. Islam SM, Saha CR (2004) J Mol Catal A: Chem 212:131-140
41. Dileep Kumar JS, Ho MM, Toyokuni T (2001) Tetrahedron Lett 42:5601-5603
42. McLaughlin MA, Barnes DM (2006) Tetrahedron Lett 47:9095-9097
43. Deka DC, Kakati HS (2006) J Chem Res 4:223-224
44. Zhang C-R, Wang Y-L (2006) Indian J Chem Sect B: Org Chem Incl Med Chem 45(2):510-511
45. Rahaim RJJ, Maleczka REJ (2005) Org Lett 7(22):5087-5090
46. Sarmah P, Dutta DK (2003) J Chem Res Synop 4:236-237
47. Banik BK, Mukhopadhyay C, Venkatraman MS, Becker FF (1998) Tetrahedron Lett 39:7243-7246
48. Banik BK, Suhendra M, Banik I, Becker FF (2000) Synthetic Commun 30(20):3745-3754
49. Desai DG, Swami SS, Hapase SB (1999) Synthetic Commun 29(6):1033-1036
50. Desai DG, Swami SS, Dabhade SK, Ghagare MG (2001) Synthetic Commun, 31(8):1249-1251
51. Kumbhar PS, Sanchez-Valente J, Millet JMM, Figueras F (2000) J Catal 191:467-473
52. (a) Aiello R, Fiscus JE, zur Loye H-C, Amiridis MD (2000) Appl Catal A: Gen 192:227-234.
53. (b) Takahashi R, Sato S, Sodesawa T, Kato M, Takenaka S, Yoshida S (2001) J Catal 204:259-271.
54. (c) Ennas G, Mei A, Musinu A, Piccaluga G, Pinna G, Solinas S (1998) J Non-Cryst Solids 232-234:587-593.
55. (d) Matsumura Y, Tode N, Yazawa T, Haruta M (1995) J Mol Catal A: Chem 99:183-185
56. (a) Xiong H, Tang S, Tang H, Zou P (2008) Carbohyd Polym 71:263-268.
57. (b) Wu KH, Chang YC, Wang GP (2004) J Magn Magn Mater 269:150-155.
58. (c) Song CF, Lu MK, Gu F, Liu SW, Wang SF, Xu D, Yuan DR (2003) Inorg Chem Commun 6(5):523-526.
59. (d) Phan NTS, Jones CW (2006) J Mol Catal A: Chem 253:123-131.