Browse > Article
http://dx.doi.org/10.5012/bkcs.2010.31.8.2195

Palladium Nanoparticles Suspended in an Ionic Liquid as Reusable Catalyst for Alkyne Semihydrogenation  

Lee, Jin-Kyu (Department of Chemistry and Research institute for Basic Sciences, Kyung Hee University)
Kim, Dae-Won (Department of Chemistry and Research institute for Basic Sciences, Kyung Hee University)
Cheong, Min-Serk (Department of Chemistry and Research institute for Basic Sciences, Kyung Hee University)
Lee, Hyun-Joo (Energy division, Korea Institute of Science and Technology)
Cho, Byung-Won (Energy division, Korea Institute of Science and Technology)
Kim, Hoon-Sik (Department of Chemistry and Research institute for Basic Sciences, Kyung Hee University)
Mukherjee, DebKumar (Department of Chemistry and Research institute for Basic Sciences, Kyung Hee University)
Publication Information
Abstract
The reaction of $PdCl_2$ dispersed in tetra-n-butylammonium bromide with tributyl amine at $120^{\circ}C$ under argon leads to stable isolable nanometric particles. X-ray diffraction analysis of the material indicated that it is constituted of Pd(0). Transmission electron microscopy analysis of the particles dispersed in acetone shows the mean particle size distribution ($4{\pm}1\;nm$). The isolated palladium nanoparticles can be dispersed in an ionic liquid or in methanol or used in solventless condition for selective hydrogenation of 2-hexyne under mild reaction conditions(0.2 MPa and $20^{\circ}C$). The commercial variety of the Lindlar catalyst was also studied for comparative investigations.
Keywords
Palladium; Nanoparticles; Semihydrogenation; Ionic liquid; Lindlar catalyst;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
Times Cited By Web Of Science : 1  (Related Records In Web of Science)
Times Cited By SCOPUS : 1
연도 인용수 순위
1 Mastalir, A.; Kiraly, Z. J. Catal. 2003, 220, 372.   DOI
2 Basile, F.; Fornasari, G.; Gazzano, M.; Vaccari, A. Appl. Clay Sci. 2000, 16, 185.   DOI
3 Choudhary, B. M.; Kantam, M. L.; Reddy, N. M.; Rao, K. K.; Harita, Y.; Bhaskar, V.; Figueras, F.; Tuel, A. Appl. Catal. A 1999, 181, 139.   DOI
4 Duca, D.; Frusteri, F.; Parmaliana, A.; Deganello, G. Appl. Catal. A 1996, 146, 269.   DOI
5 Albers, P.; Seibold, K.; Prescher, G.; Muller, H. Appl. Catal. A 1999, 176, 135.   DOI
6 Arena, F.; Cum, G.; Gallo, R.; Parmaliana, A. J. Mol. Catal. A: Chem. 1996, 110, 235.   DOI
7 Shin, E. W.; Choi, C. H.; Chang, K. S.; Na, Y. H.; Moon, S. H. Catal. Today 1998, 44, 137.   DOI
8 Asplund, S. J. Catal. 1996, 158, 267.   DOI
9 Larsson, M.; Jansson, J.; Asplund, S. J. Catal. 1998, 178, 49.   DOI
10 Edvinsson, R. K.; Holmgren, A. M.; Irandoust, S. Ind. Eng. Chem. Res. 1995, 34, 94.   DOI
11 Jackson, S. D.; Kelly, G. J. Curr. Topic Catal. 1997, 1, 47.
12 Jackson S. D.; Shaw, L. A. Appl. Catal. A 1996, 134, 91.   DOI
13 Dobrovolna, Z.; Kacer, P.; Cerveny, L. J. Mol. Catal. A. Chem. 1998, 130, 279.   DOI
14 Dupont, J.; Fonseca, G. S.; Umpierre, A. P.; Fichtner, P. F. P.; Teixeira, S. R. J. Am. Chem. Soc. 2002, 124, 4228.   DOI
15 Petro, J. In Contact Catalysis; Szabo, Z, G., Kallo, D., Eds.; Elsevier: Amsterdam, 1976; Vol. II.
16 Maier, W. F.; Chettle, S. B.; Rai, R. S.; Thomas, G. J. Am. Chem. Soc. 1986, 108, 2608.   DOI
17 Ulan, J. G.; Maier, W. F. J. Org. Chem. 1987, 52, 3132.   DOI
18 Dupont, J.; De Souza, R. F.; Suarez, P. A. Z. Chem. Rev. 2002, 102, 3667.   DOI
19 Dullius, J. E. L.; Suarez, P. A. Z.; Einloft, S.; de Souza, R. F.; Dupont, J. Organometallics 1998, 17, 815.   DOI
20 Scheeren, C. W.; Machado, G.; Dupont, J.; Fichtner, P. F. P.; Teixeira, S. R. Inorg. Chem. 2003, 42, 4738.   DOI
21 Mukherjee, D. K.; Ghosh, N. Bull. Catal. Soc. Ind. 2006, 5, 155.
22 Mukherjee, D. K. J. Nanoparticle Res. 2008, 10, 429.   DOI
23 Reetz, M. T.; Maase, M. Adv. Mater. 1999, 9, 11.
24 Semagina, N.; Renken, A.; Laub, D.; Kiwi-Minsker, L. J. Catal. 2007, 246, 308.   DOI
25 Narayanan, R.; El-Sayeed, M. A. J. Phys. Chem. B 2005, 109, 12663.   DOI   ScienceOn
26 Suarez, P. A. Z.; Dullius, J. E. L.; Einloft, S.; DeSouza, R. F.; Dupont, J. Polyhedron 1996, 15, 1217.   DOI
27 Siegel, S.; Hawkins, J. A. J. Org. Chem. 1986, 51, 1638.   DOI
28 Mastalir, A.; Kiraly, Z.; Szollosi, G.; Bartok, M. Appl. Catal. A Gen. 2001, 213, 133.
29 Astruc, D.; Lu, F.; Aranzaes, J. R. Angew. Chem. Int. Ed. 2005, 44, 7852.   DOI
30 Tessier, D.; Rakai, A.; Bozon-Verduraz, F. Bull. Soc. Chim. Fr. 1996, 133, 637.
31 Marvell, E. N.; Li, T. Synthesis 1973, 1, 457.
32 Raphael, R. A. Acetylenic Compounds in Organic Synthesis; Butterworth: Stoneham, MA, 1955.
33 Roucoux, A.; Schulz, J.; Patin, H. Chem. Rev. 2002, 102, 3757.   DOI
34 Bailey, S., King, F., Sheldon, R. A., Van Bekkum, H., Eds.; Fine Chemicals through Heterogenous Catalysis; Wiley: New York, 2001; p 351.
35 Sapkal, S. B.; Shelke, K. F.; Shingate, B. B.; Shingare, M. S. Bull. Korean Chem. Soc. 2010, 31, 351.   DOI
36 Ranu, B. C.; Chattopadhyay, K. Org. Lett. 2007, 9, 2409.   DOI
37 Hub, S.; Hilaire, L.; Touroude, R. Appl. Catal. 1988, 36, 307.   DOI
38 Boittiaux, J. P.; Cosyns, J.; Vasudevan, S. Appl. Catal. 1983, 6, 41.   DOI
39 Gigola, C. E.; Aduriz, H. R.; Bodnariuk, P. Appl. Catal. 1986, 27, 133.   DOI
40 Molnar, A.; Sarkany, A.; Varga, M. J. Mol. Catal. A Chem. 2001, 173, 185.   DOI
41 Ryndin, Y. A.; Nosova, L. V.; Boronin, A. I.; Chuvilin, A. L. Appl. Catal. 1988, 42, 131.   DOI
42 Le Bras, J.; Mukherjee, D. K.; Gonzalez, S.; Tristany, M.; Ganchegui, B.; Moreno-Manas, M.; Pleixats, R.; Henin, F.; Muzart, J. New J. Chem. 2004, 28, 1550.   DOI
43 Duca, D.; Arena, F.; Parmaliana, A.; Deganello, G. Appl. Catal. A 1998, 172, 207.   DOI
44 Duca, D.; Liotta, L. F.; Deganello, G. J. Catal. 1995, 154, 69.   DOI
45 Bensalem, A.; Bozon Verduraz, F. React. Kinet. Catal. Lett. 1997, 60, 71.   DOI