Phenyl@Rh(I)-Bridged Periodic Mesoporous Organometalsilica with High Catalytic Efficiency in Water-Medium Organic Reactions
Source abstract
Abstract
A facile approach to prepare phenyl and Rh(I) organometal bridged periodic mesoporous organometalsilica was developed based on surfactant-directed co-condensation of RhCl[PPh 2 (CH 2 ) 2 Si(OEt 3 ) 3 ] 3 and (OEt) 3 SiPhSi(OEt) 3 . The as-prepared Rh(I)-PPh 2 -PMO(Ph) exhibited matchable catalytic efficiency with the corresponding Rh(PPh 3 ) 3 Cl homogeneous catalyst in water-medium reaction between phenylboronic acid and butyl acrylate or the 1,4-conjugate addition reaction between phenylboronic acid and N, N -dimehytlacyrlmaide, which could be attributed to the high dispersion of Rh(I) active sites, the ordered mesoporous channels and the strong surface hydrophobicity resulting from phenyl fragments embedded in silica walls, leading to the facilitated the diffusion and the adsorption of organic molecules onto the catalyst in aqueous solution. The Rh(I)-PPh 2 -PMO(Ph) could be used repetitively, showing the excellent durability that could be attributed to the effective inhibition of Rh(I) leaching and the high hydrothermal stability of the mesoporous structure.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Polyoxometalates: Synthesis and Applications · Layered Double Hydroxides Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemical and Molecular Engingeering School, East China University of Science and Technology, Shanghai 200237, China
Department of Chemistry, Shanghai Normal University, Shanghai 200234, China
References (44)
Show source-provided references
1. Kresge C. T. · Nature · 1992 · 359 · 71010.1038/359710a0 ↗
2. Beck J. S. · J. Am. Chem. Soc. · 1992 · 114 · 1083410.1021/ja00053a020 ↗
3. Fujita S. · Chem. Mater. · 2008 · 20 · 89110.1021/cm702271v ↗
4. Monnier A. · Science · 1993 · 261 · 129910.1126/science.261.5126.1299 ↗
5. Zhao D. Y. · Science · 1998 · 279 · 54810.1126/science.279.5350.548 ↗
6. Meng Y. · Chem. Mater. · 2006 · 18 · 444710.1021/cm060921u ↗
7. Tian Z. R. · Science · 1997 · 276 · 92610.1126/science.276.5314.926 ↗
8. MacLachlan M. J. · Nature · 1999 · 397 · 68110.1038/17776 ↗
9. Lu Y. F. · Angew. Chem., Int. Ed. · 2006 · 45 · 766410.1002/anie.200602489 ↗
10. Inagaki S. · J. Am. Chem. Soc. · 1999 · 121 · 961110.1021/ja9916658 ↗
11. Inagaki S. · Nature · 2002 · 416 · 30410.1038/416304a ↗
12. Lu Y. F. · J. Am. Chem. Soc. · 2000 · 122 · 525810.1021/ja9935862 ↗
13. Hatton B. D. · Adv. Funct. Mater. · 2005 · 15 · 82310.1002/adfm.200400221 ↗
14. Kapoor M. P. · J. Am. Chem. Soc. · 2002 · 124 · 1517610.1021/ja0290678 ↗
15. Osborn L. A. · J. Chem. Soc. A · 1966 · 171110.1039/j19660001711 ↗
16. Shoai S. · Organometallics · 2007 · 26 · 577810.1021/om700811e ↗
17. Fukumoto Y. · Org. Lett. · 2006 · 8 · 464110.1021/ol0619415 ↗
18. Zou G. · Chem. Commun. · 2003 · 243810.1039/B305771M ↗
19. Dufaud V. · Angew. Chem., Int. Ed. · 2005 · 44 · 347510.1002/anie.200500454 ↗
20. Li C. J. · 1997
21. Lindstrom U. M. · Chem. Rev. · 2002 · 102 · 275110.1021/cr010122p ↗
22. Li C. · J. Chem. Rev. · 2005 · 105 · 309510.1021/cr030009u ↗
23. Hayashi Y. · Angew. Chem., Int. Ed. · 2006 · 45 · 810310.1002/anie.200603378 ↗
24. Sheldon R. A. · Green Chem. · 2005 · 7 · 26710.1039/b418069k ↗
25. Metivier P. · 2001
26. De Vos D. E. · 200010.1002/9783527613144 ↗
27. Corma A. · Chem. Rev. · 1997 · 97 · 237310.1021/cr960406n ↗
28. Iwasawa Y. · 198610.1007/978-94-009-5261-4 ↗
29. Li C. · Catal. Rev. · 2004 · 46 · 41910.1081/CR-200036734 ↗
30. De Vos D. E. · Chem. Rev. · 2002 · 102 · 361510.1021/cr010368u ↗
31. Li H. X. · J. Phys. Chem. B · 2006 · 110 · 2294210.1021/jp0641031 ↗
32. Li H. X. · J. Phys. Chem. C · 2008 · 112 · 636610.1021/jp0776053 ↗
33. Li H. X. · Green Chem. · 2007 · 9 · 50010.1039/b618681e ↗
34. Kröcher O. · J. Catal. · 1998 · 178 · 28410.1006/jcat.1998.2151 ↗
35. Tuysuz H. · J. Am. Chem. Soc. · 2008 · 130 · 1151010.1021/ja803362s ↗
36. Wan Y. · J. Mol. Catal. · 2006 · 258 · 8910.1016/j.molcata.2006.05.018 ↗
37. Huang H. · J. Ind. Eng. Chem. Res. · 2003 · 42 · 242710.1021/ie020440u ↗
38. Burleigh M. · J. Phys. Chem. B · 2001 · 105 · 993510.1021/jp011814k ↗
39. Hu Q. Y. · Chem. Mater. · 2005 · 17 · 156110.1021/cm0491983 ↗
40. Simon P. F. W. · Chem. Mater. · 2001 · 13 · 346410.1021/cm0110674 ↗
41. Posset T. · Chem. Mater. · 2005 · 17 · 58610.1021/cm048236f ↗
42. Margolese J. A. · Chem. Mater. · 2000 · 12 · 244810.1021/cm0010304 ↗
43. Moulder J. F. · 1992
44. Sheldon R. A. · Acc. Chem. Res. · 1998 · 31 · 48510.1021/ar9700163 ↗