Highly Stable and Magnetically Recyclable Mesoporous Silica Spheres Embedded with FeCo/Graphitic Shell Nanocrystals for Supported Catalysts
Source abstract
Abstract
We have synthesized highly stable and magnetically recyclable mesoporous silica spheres embedded with FeCo-graphitic carbon shell nanocrystals (FeCo/GC@MSS) by a simple one-step chemical vapor deposition (CVD) method. Solid core-mesoporous shell silica spheres with an average diameter of ∼400 nm are used as supports not only for the synthesis of the FeCo/GC nanocrystals but also for catalysts after the synthesis of the FeCo/GC@MSS. The FeCo/GC nanocrystals in the mesoporous silica spheres exhibit superparamagnetism with ultrahigh saturation magnetization up to 215 e.m.u./metal g at room temperature. The FeCo/GC@MSS is chemically stable against acid etching and oxidation, which enable the FeCo/GC@MSS to be used as a support for an acid catalyst, phosphomolybdic acid (PMA). We have shown that PMA-loaded FeCo/GC@MSS works as an excellent recyclable reagent system that catalyzes propargylation of 1,3-diphenyl-2-propyn-1-ol with phenol.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Catalytic Processes in Materials Science · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Inorganic and Bio-Materials Center of BK21, Sogang University, Seoul, 121-742, Korea
Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan 609-735, Korea
Department of Physics, Sogang University, Seoul, 121-742, Korea.
References (41)
Show source-provided references
1. Zhao Y. · Adv. Mater. · 2009 · 21 · 362110.1002/adma.200803645 ↗
2. Lou X. W. · Adv. Mater. · 2008 · 20 · 398710.1002/adma.200800854 ↗
3. Giri S. · Angew. Chem., Int. Ed. · 2005 · 44 · 503810.1002/anie.200501819 ↗
4. Levy L. · Chem. Mater. · 2002 · 14 · 371510.1021/cm0203013 ↗
5. Liang C. · Angew. Chem., Int. Ed. · 2008 · 47 · 369610.1002/anie.200702046 ↗
6. Xu Z. · J. Am. Chem. Soc. · 2007 · 129 · 869810.1021/ja073057v ↗
7. Lee J. · Adv. Mater. · 2006 · 18 · 207310.1002/adma.200501576 ↗
8. Yavuz C. T. · Science · 2006 · 314 · 96410.1126/science.1131475 ↗
9. Ge J. · Angew. Chem., Int. Ed. · 2007 · 46 · 434210.1002/anie.200700197 ↗
10. Lu Y. · Nano Lett. · 2002 · 2 · 18310.1021/nl015681q ↗
11. Lee K. R. · Chem. Mater. · 2008 · 20 · 673810.1021/cm802335r ↗
12. Lee B. S. · Chem. Commun. · 2010 · 46 · 393510.1039/c001255f ↗
13. Chaubey G. S. · J. Am. Chem. Soc. · 2007 · 129 · 721410.1021/ja0708969 ↗
14. Xia Y. · Adv. Mater. · 2003 · 15 · 35310.1002/adma.200390087 ↗
15. Jeong B. U. · Adv. Mater. · 2007 · 19 · 3310.1002/adma.200600674 ↗
16. Choi J. · J. Am. Chem. Soc. · 2010 · 132 · 1101510.1021/ja104503g ↗
17. Kim J. · Angew. Chem., Int. Ed. · 2008 · 47 · 843810.1002/anie.200802469 ↗
18. Jun Y. · Angew. Chem., Int. Ed. · 2008 · 47 · 512210.1002/anie.200701674 ↗
19. Ge J · Angew. Chem., Int. Ed. · 2008 · 47 · 892410.1002/anie.200803968 ↗
20. Ge J. · Nano Lett. · 2008 · 8 · 93110.1021/nl080020f ↗
21. Shokouhimehr M. · Angew. Chem., Int. Ed. · 2007 · 46 · 703910.1002/anie.200702386 ↗
22. Zhao W. · J. Am. Chem. Soc. · 2005 · 127 · 891610.1021/ja051113r ↗
23. Lin Y. S. · Chem. Mater. · 2006 · 18 · 517010.1021/cm061976z ↗
24. Deng Y. · J. Am. Chem. Soc. · 2008 · 130 · 2810.1021/ja0777584 ↗
25. Kim J. · J. Am. Chem. Soc. · 2006 · 128 · 68810.1021/ja0565875 ↗
26. Xu X. · Adv. Mater. · 2006 · 18 · 328910.1002/adma.200601546 ↗
27. Ye M. · Chem.—Eur. J. · 2010 · 16 · 624310.1002/chem.200903516 ↗
28. Hütten A. · J. Biotechnol. · 2004 · 112 · 4710.1016/j.jbiotec.2004.04.019 ↗
29. Mcguire T. R. · Appl. Phys. · 1969 · 40 · 137110.1063/1.1657506 ↗
30. Reiss G. · Nat. Mater. · 2005 · 4 · 72510.1038/nmat1494 ↗
31. Seo W. S. · Nat. Mater. · 2006 · 5 · 97110.1038/nmat1775 ↗
32. Sherlock S. P. · ACS Nano · 2010 · 5 · 150510.1021/nn103415x ↗
33. Büchel G. · Adv. Mater. · 1998 · 10 · 103610.1002/(SICI)1521-4095(199809)10:13<1036::AID-ADMA1036>3.0.CO;2-Z ↗
34. Cullity B. D. · 1978
35. Bean C. P. · J. Appl. Phys. · 1959 · 30 · 120S10.1063/1.2185850 ↗
36. Seo W. S. · Angew. Chem., Int. Ed. · 2004 · 43 · 111510.1002/anie.200352400 ↗
37. Brunauer S. · J. Am. Chem. Soc. · 1940 · 62 · 172310.1021/ja01864a025 ↗
38. Kishore Kumar G. D. · J. Org. Chem. · 2005 · 70 · 452010.1021/jo0502697 ↗
39. Das B. · Can. J. Chem. · 2008 · 86 · 70910.1139/v08-060 ↗
40. Yadav J. S. · Tetrahedron Lett. · 2009 · 50 · 396310.1016/j.tetlet.2009.04.088 ↗
41. Srihari P. · Tetrahedron Lett. · 2007 · 48 · 812010.1016/j.tetlet.2007.09.123 ↗