Highly stable noble-metal nanoparticles in tetraalkylphosphonium ionic liquids for in situ catalysis

ChemSusChem

Volumn 5, Issue 1, 2012, Pages 109-116

  Banerjee, Abhinandan ^a   Theron, Robin ^a   Scott, Robert W J ^a  

^a UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

catalysis; green chemistry; hydrogenation; ionic liquids; nanoparticles

Indexed keywords

CATALYSIS; CATALYSTS; HYDROGENATION; LITHIUM; METAL HALIDES; METALS; NANOPARTICLES; NEGATIVE IONS; ORGANIC SOLVENTS; PALLADIUM; PRECIOUS METALS; STABILIZATION; SULFUR COMPOUNDS; SUSPENSIONS (FLUIDS);

AERIAL OXIDATION; AMBIENT PRESSURES; CO-ORDINATIVELY UNSATURATED; COLLOIDAL SUSPENSIONS; GREEN CHEMISTRY; HALIDE ANIONS; HEXAFLUOROPHOSPHATES; HYDROGENATION REACTIONS; IN-SITU; LITHIUM BOROHYDRIDE; METAL NANOPARTICLES; METAL SALT; METAL SALT PRECURSORS; NANOPARTICLE SURFACE; NOBLE METAL NANOPARTICLES; PALLADIUM NANOPARTICLES; PHOSPHONIUM CATIONS; RECYCLABLE CATALYST; STERIC PROTECTION;

IONIC LIQUIDS;

ALKENE; ALKYNE; GOLD; IONIC LIQUID; METAL NANOPARTICLE; ORGANOPHOSPHORUS COMPOUND; PALLADIUM;

ARTICLE; CATALYSIS; CHEMISTRY; HYDROGENATION;

ALKENES; ALKYNES; CATALYSIS; GOLD; HYDROGENATION; IONIC LIQUIDS; METAL NANOPARTICLES; ORGANOPHOSPHORUS COMPOUNDS; PALLADIUM;

EID: 84856012201     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.201100413     Document Type: Article

References (65)

1. H. Bönnemann, W. Brijoux, R. Brinkmann, E. Dinjus, T. Joussen, B. Korall, Angew. Chem. 1991, 103, 1344-1346
2. D. Astruc, Nanoparticles and Catalysis (Ed.:, D. Astruc,), Wiley-VCH, Weinheim, 2008
3. G. Schmid, Chem. Rev. 1992, 92, 1709-1727
4. A. T. Bell, Science 2003, 299, 1688-1691
5. E. Roduner, Chem. Soc. Rev. 2006, 35, 583-592
6. T. Zeng, W.-W. Chen, C. M. Cirtiu, A. Moores, G. Song, C.-J. Li, Green Chem. 2010, 12, 570-573.
7. H. Bönnemann, G. Braun, W. Brijoux, R. Brinkmann, A. S. Tilling, K. Seevogel, K. Siepen, J. Organomet. Chem. 1996, 520, 143-162
8. C. N. R. Rao, G. U. Kulkarni, P. J. Thomas, P. P. Edwards, Chem. Soc. Rev. 2000, 29, 27-35
9. N. Toshima, T. Yonezawa, New J. Chem. 1998, 22, 1179-1201
10. C. M. Cirtiu, A. F. Dunlop-Brière, A. Moores, Green Chem. 2011, 13, 288-291.
11. A. Biffis, S. Cunial, P. Spontoni, L. Prati, J. Catal. 2007, 251, 1-6
12. C. Rangheard, C. d. J. Fernandez, P.-H. Phua, J. Hoorn, L. Lefort, J. G. De Vries, Dalton Trans. 2010, 39, 8464-8471
13. S. M. Zhang, C. L. Zhang, J. W. Zhang, Z. J. Zhang, H. X. Dang, Z. S. Wu, W. M. Liu, Acta Phys. Chim. Sin. 2004, 20, 554-556.
14. A. Safavi, S. Zeinali, Colloids Surf. A 2010, 362, 121-126
15. G. S. Fonseca, J. B. Domingos, F. Nome, J. Dupont, J. Mol. Catal. A: Chem. 2006, 248, 10-16
16. Y. S. Salprima, R. N. Dhital, H. Sakurai, Tetrahedron Lett. 2011, 52, 2633-2637.
17. H.-C. Schwarzer, W. Peukert, AIChE J. 2004, 50, 3234-3247
18. M. Manteghian, S. Ghader, Chem. Eng. Technol. 2009, 32, 835-839.
19. K. S. Nagabhushana, H. Bönnemann, Nanotechnol. Catal., Vol. 1 (Eds.:, B. Zhou, S. Hermans, G. A. Somorjai,), Springer, New York, 2004, pp. 51-72
20. N. Yan, Y. Yuan, P. J. Dyson, Chem. Commun. 2011, 47, 2529-2531
21. V. Calõ, A. Nacci, A. Monopoli, A. Detomaso, P. Iliade, Organometallics 2003, 22, 4193-4197
22. X. Mu, J. Meng, Z. Li, Y. Kou, J. Am. Chem. Soc. 2005, 127, 9694-9695
23. B. Léger, A. Denicourt-Nowicki, H. Olivier-Bourbigou, A. Roucoux, ChemSusChem 2008, 1, 984-987.
24. D. Astruc, F. Lu, J. R. Aranzaes, Angew. Chem. 2005, 117, 8062-7872
25. J. Dupont, D. de Oliviera Silva, Nanoparticles and Catalysis (Ed.:, D. Astruc,), Wiley-VCH, Weinheim, 2008, Chapter 6, p. 195
26. P. Migowski, J. Dupont, Chem. Eur. J. 2007, 13, 32-39
27. J. Huang, T. Jiang, H. X. Gao, B. X. Han, Z. M. Liu, W. Z. Wu, Y. H. Chang, G. Y. Zhao, Angew. Chem. 2004, 116, 1421-1423
28. Angew. Chem. Int. Ed. 2004, 43, 1397-1399.
29. P. A. Z. Suarez, J. E. L. Dullius, S. Einloft, R. F. DeSouza, J. Dupont, Polyhedron 1996, 15, 1217-1219
30. J. Dupont, G. S. Fonseca, A. P. Umpierre, P. F. P. Fichtner, S. R. Teixeira, J. Am. Chem. Soc. 2002, 124, 4228-4229
31. G. S. Fonseca, A. P. Umpierre, P. F. P. Fichtner, S. R. Teixeira, J. Dupont, Chem. Eur. J. 2003, 9, 3263-3269.
32. V. Calò, A. Nacci, A. Monopoli, A. Fornaro, L. Sabbatini, N. Cioffi, N. Ditaranto, Organometallics 2004, 23, 5154-5158
33. M. Moreno-Mañas, R. Pleixats, Acc. Chem. Res. 2003, 36, 638-643
34. J. G. de Vries, Dalton Trans. 2006, 421-429.
35. P. Dash, N. A. Dehm, R. W. J. Scott, J. Mol. Catal. A: Chem. 2008, 286, 114-119
36. P. Dash, S. Miller, R. W. J. Scott, J. Mol. Catal. A: Chem. 2010, 329, 86-95.
37. M. Freemantle, An Introduction to Ionic Liquids, RSC Publishing, Cambridge, 2010
38. F. M. Kerton, Alternative Solvents for Green Chemistry, RSC Publishing, Cambridge, 2009
39. T. Welton, Green Chem. 2011, 13, 225
40. J. P. Hallett, T. Welton, Chem. Rev. 2011, 111, 3508-3576.
41. P. Dash, R. W. J. Scott, Chem. Commun. 2009, 812-814.
42. L. Luo, N. Yu, R. Tan, Y. Jin, D. Yin, D. Yin, Catal. Lett. 2009, 130, 489-495
43. A. Stojanovic, D. Kogelnig, L. Fischer, S. Hann, M. Galanski, M. Groessl, R. Krachler, B. K. Keppler, Aust. J. Chem. 2010, 63, 511-524
44. K. S. Kim, D. Demberelnyamba, H. Lee, Langmuir 2004, 20, 556-560
45. C. Vilain, F. Goettmann, A. Moores, P. Le Floch, C. Sanchez, J. Mater. Chem. 2007, 17, 3509-3514.
46. L. G. Sánchez, J. R. Espel, F. Onink, G. W. Meindersma, A. B. de Haan, J. Chem. Eng. Data 2009, 54, 2803-2812.
47. L. S. Ott, M. L. Cline, M. Deetlefs, K. R. Seddon, R. G. Finke, J. Am. Chem. Soc. 2005, 127, 5758-5759.
48. M. G. Freire, C. M. S. S. Neves, I. M. Marrucho, J. A. P. Coutinho, A. M. Fernandes, J. Phys. Chem. A 2010, 114, 3744-3749.
49. L. Ford, F. Atefi, R. D. Singer, P. J. Scammells, Eur. J. Org. Chem. 2011, 942-950.
50. M.-C. Tseng, H.-C. Kan, Y.-H. Chu, Tetrahedron Lett. 2007, 48, 9085-9089.
51. H. A. Kalviri, F. M. Kerton, Green Chem. 2011, 13, 681-686.
52. Z. Yinghuai, E. Widjaja, S. L. P. Sia, W. Zhan, K. Carpenter, J. A. Maguire, N. S. Hosmane, M. F. Hawthorne, J. Am. Chem. Soc. 2007, 129, 6507-6512.
53. E. Guyonnet Bilé, R. Sassine, A. Denicourt-Nowicki, F. Launay, A. Roucoux, Dalton Trans. 2011, 40, 6524-6531.
54. M. Dasog, R. W. J. Scott, Langmuir 2007, 23, 3381-3387.
55. H. Bönnemann, K. S. Nagabhushana, Surface and Nanomolecular Catalysis (Ed.:, R. Richards,), Taylor and Francis, London 2006, Chapter 3, p. 63-73.
56. C. Hardacre, J. D. Holbrey, S. E. J. McMath, D. T. Bowron, A. K. Soper, J. Chem. Phys. 2003, 118, 273-278
57. P. J. Dyson, J. S. McIndoe, D. B. Zhao, Chem. Commun. 2003, 508-509.
58. O. R. Miranda, N. R. Dollahon, T. S. Ahmadi, Cryst. Growth Des. 2006, 6, 2747-2753
59. F. X. Chen, G. Q. Xu, T. S. A. Hor, Mater. Lett. 2003, 57, 3282-3286.
60. J. Kumełan, A. P.-S. Kamps, D. Tuma, G. Maurer, J. Chem. Eng. Data 2006, 51, 1364-1367.
61. J. L. Anthony, J. L. Anderson, E. J. Maginn, J. F. Brennecke, J. Phys. Chem. B 2005, 109, 6366-6374
62. P. J. Dyson, G. Laurenczy, C. A. Ohlin, J. Vallance, T. Welton, Chem. Commun. 2003, 2418-2419.
63. L. Ferguson, P. Scovazzo, Ind. Eng. Chem. Res. 2007, 46, 1369-1374.
64. C. J. Bradaric, A. Downard, C. Kennedy, A. J. Robertson, Y. H. Zhou, Green Chem. 2003, 5, 143-152.
65. G. H. Woehrle, J. E. Hutchison, S. Ozkar, R. G. Finke, Turk. J. Chem. 2006, 30, 1-13.