Ion- and atom-leaching mechanisms from palladium nanoparticles in cross-coupling reactions

被引:222
作者
Gaikwad, Anil V.
Holuigue, Alexandre
Thathagar, Mehul B.
ten Elshof, Johan E.
Rothenberg, Gadi
机构
[1] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1018 WV Amsterdam, Netherlands
[2] DSM Pharma Chem, NL-6160 MD Geleen, Netherlands
[3] Univ Twente, MESA Inst Nanotechnol, NL-7500 AE Enschede, Netherlands
关键词
catalysis; cross-coupling; Heck reaction; membranes nanoparticles;
D O I
10.1002/chem.200700105
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Leaching of palladium species from Pd nanoparticles under C-C coupling conditions was observed for both Heck and Suzuki reactions by using a special membrane reactor. The membrane allows the passage of palladium atoms and ions, but not of species larger than 5 nm. Three possible mechanistic scenarios for palladium leaching were investigated with the aim of identifying the true catalytic species. Firstly, we examined whether or not palladium(0) atoms could leach from clusters under non-oxidising conditions. By using our membrane reactor, we proved that this indeed happens. We then investigated whether or not small palladium(0) clusters could in fact be the active catalytic species by analysing the reaction composition and the palladium species that diffused through the membrane. Neither TEM nor ICP analysis supported this scenario. Finally, we tested whether or not palladium(II) ions could be leached in the presence of Phi by oxidative addition and the formation of [(PdArI)-Ar-II] complexes. Using mass spectrometry, UV-visible spectroscopy and (CNMR)-C-13 spectroscopy, we observed and monitored the formation and diffusion of these complexes, which showed that the first and the third mechanistic scenarios were both possible, and were likely to occur simultaneously. Based on these findings, we maintain that palladium nanoparticles are not the true catalysts in C-C coupling reactions. Instead, catalysis is carried out by either palladium(0) atoms or palladium(II) ions that leach into solution.
引用
收藏
页码:6908 / 6913
页数:6
相关论文
共 63 条
[11]   CLUSTERS, COLLOIDS AND CATALYSIS [J].
BRADLEY, JS ;
HILL, E ;
LEONOWICZ, ME ;
WITZKE, H .
JOURNAL OF MOLECULAR CATALYSIS, 1987, 41 (1-2) :59-74
[12]   Combinatorial explosion in homogeneous catalysis: Screening 60,000 cross-coupling reactions [J].
Burello, E ;
Farrusseng, D ;
Rothenberg, G .
ADVANCED SYNTHESIS & CATALYSIS, 2004, 346 (13-15) :1844-1853
[13]   Functional resins in palladium catalysis: Promising materials for Heck reaction in aprotic polar solvents [J].
Caporusso, AM ;
Innocenti, P ;
Aronica, LA ;
Vitulli, G ;
Gallina, R ;
Biffis, A ;
Zecca, M ;
Corain, B .
JOURNAL OF CATALYSIS, 2005, 234 (01) :1-13
[14]   The role of Pd nanoparticles in ionic liquid in the Heck reaction [J].
Cassol, CC ;
Umpierre, AP ;
Machado, G ;
Wolke, SI ;
Dupont, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (10) :3298-3299
[15]   Layered double hydroxide supported nanopalladium catalyst for Heck-, Suzuki-, Sonogashira-, and Stille-type coupling reactions of chloroarenes [J].
Choudary, BM ;
Madhi, S ;
Chowdari, NS ;
Kantam, ML ;
Sreedhar, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (47) :14127-14136
[16]   Development and comparative study of different nanofiltration membranes for recovery of highly charged large ions [J].
Chowdhury, SR ;
ten Elshof, JE ;
Benes, NE ;
Keizer, K .
DESALINATION, 2002, 144 (1-3) :41-46
[17]   Kinetics and mechanistic aspects of the Heck reaction promoted by a CN-palladacycle [J].
Consorti, CS ;
Flores, FR ;
Dupont, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (34) :12054-12065
[18]   Basic zeolites containing palladium as bifunctional heterogeneous catalysts for the Heck reaction [J].
Corma, A ;
García, H ;
Leyva, A ;
Primo, A .
APPLIED CATALYSIS A-GENERAL, 2003, 247 (01) :41-49
[19]   Kinetic studies of the oxidative addition and transmetallation steps involved in the cross-coupling of alkynyl stannanes with aryl iodides catalysed by η2-(dimethyl fumarate)(iminophosphane)palladium(0) complexes [J].
Crociani, B ;
Antonaroli, S ;
Canovese, L ;
Uguagliati, P ;
Visentin, F .
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2004, (04) :732-742
[20]   Mercaptopropyl-modified mesoporous silica: A remarkable support for the preparation of a reusable, heterogeneous palladium catalyst for coupling reactions [J].
Crudden, CM ;
Sateesh, M ;
Lewis, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (28) :10045-10050