2006
DOI: 10.1002/adsc.200606163
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New Heterogenized Gold(I)‐Heterocyclic Carbene Complexes as Reusable Catalysts in Hydrogenation and Cross‐Coupling Reactions

Abstract: Abstract:Mononuclear unsymmetrical N-heterocyclic carbene-gold complexes and the corresponding solid catalysts in which a gold-carbene complex has been immobilized on silica gel, ordered mesoporous silica (MCM-41), and delaminated zeolite (ITQ-2) have been prepared. These new catalysts have been tested in the hydrogenation of alkenes and the Suzuki cross-coupling reaction to afford selectively non-symmetrical biaryls. These reactions were studied with the soluble as well as with the heterogenized counterpart c… Show more

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Cited by 160 publications
(82 citation statements)
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“…Corma et al [227] prepared Au/MCM-41 (loading of 0.20-30 mmol-Au/g support) using a gold-carbene complex [(carbene)AuCl] as Au precursor. The resulting catalysts were active for the hydrogenation of alkenes and the Suzuki cross-coupling reaction between halobenzene and arylboronic acids.…”
Section: Other Methods Of Synthesismentioning
confidence: 99%
“…Corma et al [227] prepared Au/MCM-41 (loading of 0.20-30 mmol-Au/g support) using a gold-carbene complex [(carbene)AuCl] as Au precursor. The resulting catalysts were active for the hydrogenation of alkenes and the Suzuki cross-coupling reaction between halobenzene and arylboronic acids.…”
Section: Other Methods Of Synthesismentioning
confidence: 99%
“…144 Interestingly, mononuclear NHC carbine-gold complexes were also covalently grafted on delaminated ITQ-2 zeolite for hydrogenation of alkenes and for Suzuki cross-coupling reaction, yielding selectively non-symmetrical biaryls. 145 Related with this last approach, Au(I) and Pd(II) complexes were heterogenized onto ITQ-2, obtaining effective catalysts for Sonogashira cross-coupling reactions between iodobenzene and arylboronic acids or alkynes. 146 Stabilized enzymes were also covalently supported onto MWW layers which are forming ITQ-2 zeolites, generating novel biocatalysts.…”
Section: 131mentioning
confidence: 99%
“…In most of the cases, the steps required are: a) synthesis of the layered inorganic precursor; b) swelling and pillarization of starting layered precursors; c) extraction and post-functionalization processes. 28,29,30,31 As can be seen, the multi-step synthesis method involves a long route that, on top, requires recovery and isolation of intermediate lamellar hybrid solids. Moreover, it is difficult to avoid an inhomogeneous distribution of organic pillars located in the interlayer space, which could be a problem during the catalytic reactions.…”
Section: Introductionmentioning
confidence: 99%