journal article·2015-01-28

Organoamine-Functionalized Graphene Oxide as a Bifunctional Carbocatalyst with Remarkable Acceleration in a One-Pot Multistep Reaction

Fang Zhang, Huangyong Jiang, Xiaotao Wu, Zhan Mao, Hexing Li

Publisher page

Abstract

In this work, we reported the synthesis of bifunctional carbocatalyst with acid-base dual-activation mechanism by introducing organoamines on the basal planes of graphene oxide (GO). Interestingly, GO-supported primary amine (AP-GO) exclusively promoted one-pot Henry-Michael reactions with excellent activity to give synthetically valuable multifunctionalized nitroalkanes. Notably, it also exhibited significantly higher activity than those using propylamine, activated carbon-supported primary amine, and mesoporous silica-supported primary amine as the catalysts. This superior catalytic performance originated from the unique properties of AP-GO, which provided the acid-base cooperative effect by the appropriate positioning of primary amines on their basal planes and carboxyl acids along their edges and the decreased diffusion resistance of the reactants and the intermediates during the multistep catalytic cycles because of its open two-dimensional sheet-like structure. Moreover, it could be readily recycled by simple filtration and subsequently reused without significant loss of its catalytic activity in a six times run test.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanomaterials for catalytic reactions · Advanced Photocatalysis Techniques · Covalent Organic Framework Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

The Education Ministry Key Lab of Resource Chemistry and Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University, Shanghai 200234, P. R. China

Funding

Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Shanghai Government

References (59)

Show source-provided references
1. Margelefsky E. L. · Chem. Soc. Rev. · 2008 · 37 · 111810.1039/b710334b ↗
2. Brunelli N. A. · J. Catal. · 2013 · 308 · 6010.1016/j.jcat.2013.05.022 ↗
3. Tietze L. F. · 200610.1002/9783527609925 ↗
4. Allen A. E. · Chem. Sci. · 2012 · 3 · 63310.1039/c2sc00907b ↗
5. Ambrosini L. M. · ChemCatChem. · 2010 · 2 · 137310.1002/cctc.200900323 ↗
6. Du J. · Science · 2014 · 344 · 39210.1126/science.1251511 ↗
7. Krautwald S. · Science · 2013 · 340 · 106510.1126/science.1237068 ↗
8. Ibrahem I. · Angew. Chem., Int. Ed. · 2013 · 52 · 87810.1002/anie.201208634 ↗
9. Pellissier H. · Tetrahedron · 2013 · 69 · 717110.1016/j.tet.2013.06.020 ↗
10. Köhler V. · Nat. Chem. · 2013 · 5 · 9310.1038/nchem.1498 ↗
11. Benaglia M. · 200910.1002/9780470682005 ↗
12. Gruttadauria M. · Chem. Soc. Rev. · 2008 · 37 · 166610.1039/b800704g ↗
13. Noda H. · Angew. Chem., Int. Ed. · 2012 · 51 · 801710.1002/anie.201203066 ↗
14. Climent M. J. · Chem. Rev. · 2011 · 111 · 107210.1021/cr1002084 ↗
15. Hermannsdörfer J. · Angew. Chem., Int. Ed. · 2012 · 51 · 1147310.1002/anie.201205078 ↗
16. Climent M. J. · ACS Catal. · 2014 · 4 · 87010.1021/cs401052k ↗
17. Zhao M. T. · J. Am. Chem. Soc. · 2014 · 136 · 173810.1021/ja411468e ↗
18. Zheng Y. · Angew. Chem., Int. Ed. · 2013 · 52 · 311010.1002/anie.201209548 ↗
19. Yu H. · Angew. Chem., Int. Ed. · 2011 · 50 · 397810.1002/anie.201007932 ↗
20. Kumar B. · Nat. Commun. · 2013 · 4 · 281910.1038/ncomms3819 ↗
21. Haag D. · Top. Catal. · 2014 · 57 · 76210.1007/s11244-013-0233-9 ↗
22. Rueping M. · Green Chem. · 2011 · 13 · 108410.1039/c1gc15027h ↗
23. Shylesh S. · ChemCatChem. · 2011 · 3 · 27810.1002/cctc.201000353 ↗
24. Huang Y. L. · Angew. Chem., Int. Ed. · 2011 · 50 · 66110.1002/anie.201004572 ↗
25. Notestein J. M. · Chem.—Eur. J. · 2006 · 12 · 395410.1002/chem.200501152 ↗
26. Motokura K. · Angew. Chem., Int. Ed. · 2008 · 47 · 923010.1002/anie.200802515 ↗
27. Phan N. T. S. · Angew. Chem., Int. Ed. · 2006 · 45 · 220910.1002/anie.200503445 ↗
28. Felpin F. · ChemSusChem · 2008 · 1 · 71810.1002/cssc.200800110 ↗
29. Deiana L. · Angew. Chem., Int. Ed. · 2014 · 53 · 344710.1002/anie.201310216 ↗
30. Motokura K. · J. Am. Chem. Soc. · 2007 · 129 · 954010.1021/ja0704333 ↗
31. Yang Y. · Angew. Chem., Int. Ed. · 2012 · 51 · 916410.1002/anie.201204829 ↗
32. Su D. S. · Chem. Rev. · 2013 · 113 · 578210.1021/cr300367d ↗
33. Navalon S. · Chem. Rev. · 2014 · 114 · 617910.1021/cr4007347 ↗
34. Wang Y. · Angew. Chem., Int. Ed. · 2012 · 51 · 6810.1002/anie.201101182 ↗
35. Su C. L. · Acc. Chem. Res. · 2013 · 46 · 227510.1021/ar300118v ↗
36. Dreyer D. R. · Chem. Sci. · 2011 · 2 · 123310.1039/c1sc00035g ↗
37. Dreyer D. R. · Chem. Soc. Rev. · 2014 · 43 · 528810.1039/C4CS00060A ↗
38. Jia H. · Adv. Synth. Catal. · 2011 · 353 · 52810.1002/adsc.201000748 ↗
39. Basu B. · RSC Adv. · 2013 · 3 · 2213010.1039/c3ra44712j ↗
40. Zhang W. · Nanoscale · 2013 · 5 · 603010.1039/c3nr01323e ↗
41. Rodrigo E. · Chem. Commun. · 2014 · 50 · 627010.1039/c4cc02701a ↗
42. Zhang F. · ACS Catal. · 2014 · 4 · 39410.1021/cs400761r ↗
43. Sengupta D. · Tetrahedron Lett. · 2014 · 55 · 659610.1016/j.tetlet.2014.10.043 ↗
44. Liang Y. · Nat. Mater. · 2011 · 10 · 78010.1038/nmat3087 ↗
45. Shi P. · Appl. Catal., B · 2012 · 123 · 26510.1016/j.apcatb.2012.04.043 ↗
46. Wang S. · J. Phys. Chem. Lett. · 2012 · 3 · 233210.1021/jz300930u ↗
47. Burkett S. L. · Chem. Commun. · 1996 · 11 · 136710.1039/CC9960001367 ↗
48. Chong A. S. M. · J. Phys. Chem. B · 2003 · 107 · 1265010.1021/jp035877+ ↗
49. Jun Y. · J. Phys. Chem. C · 2007 · 111 · 1307610.1021/jp072606g ↗
50. Fu Y. · J. Mater. Chem. A · 2013 · 1 · 266310.1039/c2ta00353h ↗
51. Zhang F. · Green Chem. · 2013 · 15 · 166510.1039/c3gc40215k ↗
52. Lomeda J. R. · J. Am. Chem. Soc. · 2008 · 130 · 1620110.1021/ja806499w ↗
53. Zeidon R. K. · Angew. Chem., Int. Ed. · 2006 · 45 · 633210.1002/anie.200602243 ↗
54. Zeidon R. K. · J. Catal. · 2007 · 247 · 37910.1016/j.jcat.2007.02.005 ↗
55. Sharma K. K. · Angew. Chem., Int. Ed. · 2007 · 46 · 287910.1002/anie.200604570 ↗
56. Bass J. D. · J. Am. Chem. Soc. · 2006 · 128 · 373710.1021/ja057395c ↗
57. Kandel K. · J. Catal. · 2012 · 291 · 6310.1016/j.jcat.2012.04.005 ↗
58. Xue T. · Angew. Chem., Int. Ed. · 2012 · 51 · 382210.1002/anie.201108400 ↗
59. Liu X. · Angew. Chem., Int. Ed. · 2014 · 53 · 762410.1002/anie.201404543 ↗