Immobilized Pd nanoparticles on Tris-modified SiO2: Synthesis, characterization, and catalytic activity in Heck cross-coupling reactions

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 35, Issue 9, 2014, Pages 1547-1554

  Hajipour, Abdol R ^a,b   Azizi, Ghobad ^a  

^a ISFAHAN UNIVERSITY OF TECHNOLOGY   (Iran)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Carbon carbon coupling reaction; Heck coupling; Heterogeneous catalyst; Supported palladium nanoparticle

Indexed keywords

CATALYST ACTIVITY; COMPUTER SOFTWARE REUSABILITY; LEACHING; NANOPARTICLES; PALLADIUM; SYNTHESIS (CHEMICAL); TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION; X RAY SPECTROSCOPY;

CATALYTIC APPLICATIONS; FIELD EMISSION SCANNING ELECTRON MICROSCOPY; HECK CROSS-COUPLING REACTION; HETEROGENEOUS CATALYST; REACTION CONDITIONS; REACTION PARAMETERS; REUSABLE CATALYSTS; TRISHYDROXYMETHYLAMINOMETHANE;

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EID: 84906856538     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1872-2067(14)60109-1     Document Type: Article

References (33)

1. Turner M, Golovko V B, Vaughan O P H, Abdulkin P, Berenguer-Murcia A, Tikhov M S, Johnson B F G, Lambert R M. Nature, 2008, 454: 981
2. Astruc D, Lu F, Aranzaes J R. Angew Chem Int Ed, 2005, 44: 7852
3. Beletskaya I P, Cheprakov A V. Chem Rev, 2000, 100: 3009
4. de Vries J G. Can J Chem, 2001, 79: 1086
5. Pirisedigh A, Zarei A, Seyedjamali H, Khazdooz L, Hajipour A R. Monatsh Chem, 2012, 143: 791
6. Saha M, Pal A K. Tetrahedron Lett, 2011, 52: 4872
7. Zarei A, Khazdooz L, Pirisedigh A, Hajipour A R, Seyedjamali H, Aghaei H. Tetrahedron Lett, 2011, 52: 4554
8. Hajipour A R, Rafiee F. J Organomet Chem, 2011, 696: 2669
9. Hajipour A R, Rafiee F. App Organomet Chem, 2011, 25: 542
10. Karimi B, Enders D. Org Lett, 2006, 8: 1237
11. Schönfelder D, Nuyken O, Weberskirch R. J Organomet Chem, 2005, 690: 4648
12. Gruber-Woelfler H, Radaschitz P F, Feenstra P W, Haas W, Khinast J G. J Catal, 2012, 286: 30
13. Polshettiwar V, Varma R S. Org Biomol Chem, 2009, 7: 37
14. Polshettiwar V, Hesemann P, Moreau J J E. Tetrahedron, 2007, 63: 6784
15. Uozumi Y, Kimura T. Synlett, 2002: 2045
16. Bakherad M, Keivanloo A, Samangooei S. Chin. J. Catal, 2014, 35: 324-328
17. Chen G F, Wang F, Wang Y H, Zhang X C, Qin H Q, Zou H F, Xu J. Chin J Catal, 2014, 35: 540
18. Feng Y J, Li L, Li Y S, Zhao W R, Gu J L, Shi J L. J Mol Catal A, 2010, 322: 50
19. Zhang F W, Jin J, Zhong X, Li S W, Niu J R, Li R, Ma J T. Green Chem, 2011, 13: 1238
20. Yang X, Fei Z F, Zhao D, Ang W H, Li Y D, Dyson P J. Inorg Chem, 2008, 47: 3292
21. Tao R T, Miao S D, Liu Z M, Xie Y, Han B X, An G M, Ding K L. Green Chem, 2009, 11: 96
22. Senapati K K, Roy S, Borgohain C, Phukan P. J Mol Catal A, 2012, 352: 128
23. Proch S, Mei Y, Villanueva J M R, Lu Y, Karpov A, Ballauff M, Kempe R. Adv Synth Catal, 2008, 350: 493
24. Liu G, Hou M Q, Song J Y, Jiang T, Fan H L, Zhang Z F, Han B X. Green Chem, 2010, 12: 65
25. Ko S, Jang J. Angew Chem Int Ed, 2006, 45: 7564
26. Costa N J S, Kiyohara P K, Monteiro A L, Coppel Y, Philippot K, Rossi L M. J Catal, 2010, 276: 382
27. Corma A, Iborra S, Llabrés i Xamena F X, Montón R, Calvino J J, Prestipino C. J Phys Chem C, 2010, 114: 8828
28. Cirtiu C M, Dunlop-Briere A F, Moores A. Green Chem, 2011, 13: 288
29. Boudjahem A-G, Mokrane T, Redjel A, Bettahar M M. C R Chim, 2010, 13: 1433
30. Yang H Q, Han X J, Li G, Wang Y W. Green Chem, 2009, 11: 1184
31. Polshettiwar V, Molnár Á;. Tetrahedron, 2007, 63: 6949
32. Richardson J M, Jones C W. J Catal, 2007, 251: 80
33. Zhao F Y, Shirai M, Ikushima Y, Arai M. J Mol Catal A, 2002, 180: 211