Palladium(0) nanoparticles formed in situ in the Suzuki-Miyaura reaction: The effect of a palladium(II) precursor

Applied Catalysis A: General

Volumn 378, Issue 1, 2010, Pages 83-89

  Borkowski, T ^a   Trzeciak, A M ^a   Bukowski, W ^b   Bukowska, A ^b   Tylus, W ^c   Kepinski L ^d  

^a UNIVERSITY OF WROC AW   (Poland)

^b RZESZOW UNIVERSITY OF TECHNOLOGY   (Poland)

^c WROCLAW UNIVERSITY OF TECHNOLOGY   (Poland)

^d INSTITUTE OF LOW TEMPERATURE AND STRUCTURE RESEARCH   (Poland)

Author keywords

Immobilized catalyst; Nanoparticles; Palladium; Suzuki Miyaura; XPS

Indexed keywords

CATALYTIC PERFORMANCE; CATALYTIC PROCESS; GLYCIDYL METHACRYLATE; IMMOBILIZED CATALYST; IMMOBILIZED CATALYSTS; IN-SITU; PALLADIUM CATALYST; PALLADIUM PRECURSORS; PRE-TREATMENT; SEM; SUZUKI-MIYAURA; SUZUKI-MIYAURA REACTION; TEM; XPS;

ACRYLIC MONOMERS; AGGLOMERATION; CATALYSTS; CHEMICAL REACTIONS; NANOPARTICLES; PALLADIUM COMPOUNDS; X RAY PHOTOELECTRON SPECTROSCOPY;

PALLADIUM;

EID: 77949491344     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2010.02.004     Document Type: Article

References (44)

1. In: Cornils B., and Herrmann W.A. (Eds). Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook in Two Volumes (1996), VCH, Weinheim
2. In: Diederich F., and Stang P.J. (Eds). Metal-Catalyzed Cross-Coupling Reactions (1997), VCH, Weinheim
3. In: Beller M. (Ed). Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals (2004), VCH, Weinheim
4. Beletskaya I.P., and Cheprakov A.V. Chem. Rev. 100 (2000) 3009-3066
5. Trzeciak A.M., and Ziółkowski J.J. Coord. Chem. Rev. 249 (2005) 2308-2322
6. Trzeciak A.M., and Ziółkowski J.J. Coord. Chem. Rev. 251 (2007) 1281-1293
7. Tsuji J. Palladium Reagents and Catalysis. New Perspectives for the 21th Century (2004), John Wiley & Sons, Ltd.
8. Miyaura N., Yanagi T., and Suzuki A. Synth. Commun. 11 (1981) 513-519
9. Miyaura N., and Suzuki A. Chem. Rev. 95 (1995) 2457-2483
10. Suzuki A. J. Organomet. Chem. 576 (1999) 147-168
11. Polshettiwar V., and Varma R.S. Acc. Chem. Res. 41 (2008) 629-639
12. Arvela R.K., Leadbeater N.E., Sangi M.S., Wiliams V.A., Granados P., and Singer R.D. J. Org. Chem. 70 (2005) 161-168
13. Bellina F., Carpita A., and Rossi R. Synthesis (2004) 2419-2440
14. Bedford R.B., Cazin C.S.J., and Holder D. Coord. Chem. Rev. 248 (2004) 2283-2321
15. Phan N.T.S., Van Der Sluys M., and Jones C.W. Adv. Synth. Catal. 348 (2006) 609-679
16. Beller M., Fischer H., Herrmann W.A., Ofele K., and Brossner C. Angew. Chem. Int. Ed. Engl. 34 (1995) 1848-1849
17. Andrus M.B., and Song C. Org. Lett. 3 23 (2001) 3761-3764
18. Kantchev E.A.B., O'Brien C.J., and Organ M.G. Aldrichim. Acta 39 (2006) 97-111
19. Navarro O., Kelly III R.A., and Nolan S.P. J. Am. Chem. Soc. 125 (2003) 16194-16195
20. McLachlan F., Mathews C.J., Smith P.J., and Welton T. Organometallics 22 (2003) 5350-5357
21. Bedford R.B., Cazin C.S.J., Hursthouse M.B., Light M.E., and Scordia V.J.M. Dalton Trans. (2004) 3864-3868
22. Alimardanov A., Schmieder-van de Vondervoort L., de Vries A.H.M., and De Vries J.G. Adv. Synth. Catal. 346 (2004) 1812-1817
23. Reetz M.T., and Westermann E. Angew. Chem. Int. Ed. 39 1 (2000) 165-168
24. De Vries J.G. Dalton Trans. (2006) 421-429
25. Astruc D. Inorg. Chem. 46 (2007) 1884-1894
26. Hu J., and Liu Y. Langmuir 21 (2005) 2121-2123
27. Köhler K., Heidenreich R.G., Soomro S.S., and Pröckl S.S. Adv. Synth. Catal. 350 (2008) 2930-2936
28. Li Y., Hong M.X., Collard M.D., and El-Sayed A.M. Org. Lett. 2 (2000) 2385-2388
29. Narayanan R., and El-Sayed M.A. J. Catal. 234 (2005) 348-355
30. Narayanan R., and El-Sayed M.A. J. Am. Chem. Soc. 125 (2003) 8340-8347
31. Yang X., Fei Z., Zhao D., Ang W.H., and Dyson P.J. Inorg. Chem. 47 (2008) 3292-3297
32. Felpin F.-X., Ayad T., and Mitra S. Eur. J. Org. Chem. (2006) 2679-2690
33. Kantam M.L., Roy S., Roy M., Sreedhar B., and Choudary B.M. Adv. Synth. Catal. 347 15 (2005) 2002-2008
34. Kabalka G.W., Pagui R.M., and Hair C.M. Org. Lett. 1 9 (1999) 1423-1425
35. Kudo D., Masui Y., and Onaka M. Chem. Lett. 36 7 (2007) 918-919
36. Gniewek A., Ziółkowski J.J., Trzeciak A.M., Zawadzki M., Grabowska H., and Wrzyszcz J. J. Catal. 254 (2008) 121-130
37. Kleist W., Lee J.-K., and Köhler K. Eur. J. Inorg. Chem. (2009) 261-266
38. Webb J.D., MacQuarrie S., McEleney K., and Crudden C.M. J. Catal. 252 (2007) 97-109
39. Cwik A., Hell Z., and Figueras F. Org. Biol. Chem. 3 24 (2005) 4307-4309
40. Choudary B.M., Mahdi S., Chowdari N.S., Kantam M.L., and Sreedhar B. J. Am. Chem. Soc. 124 (2002) 14127-14136
41. Corma A., Garcia H., and Leyva A. Appl. Catal. A 236 (2002) 179-185
42. Okumura K., Matsui H., Sanada T., Arao M., Honma T., Hirayama S., and Niwa M. J. Catal. 265 (2009) 89-98
43. Trzeciak A.M., Mieczyńska E., Ziólkowski J.J., Bukowski W., Bukowska A., Noworól J., and Okal J. New J. Chem. 32 (2008) 1124-1130
44. Huang L., Wong P.K., Tan J., Ang T.P., and Wang Z. J. Phys. Chem. C 113 (2009) 10120-10130