2013
DOI: 10.1002/adsc.201300753
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Palladium Nanoparticles in Glycerol: A Versatile Catalytic System for CX Bond Formation and Hydrogenation Processes

Abstract: Palladium nanoparticles stabilised by tris(3-sulfophenyl)phosphine trisodium salt in neat glycerol have been synthesised and fully characterised, starting from both Pd(II) and Pd(0) species. The versatility of this innovative catalytic colloidal solution has been proved by its efficient application in C À X bond formation processes (X = C, N, P, S) and C À C multiple bond hydrogenation reactions. The catalytic glycerol phase could be recycled more than ten times, preserving its activity and selectivity. The sc… Show more

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Cited by 61 publications
(63 citation statements)
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“…5%), in addition to the corresponding ethyl derivatives 5 and 6. A similar catalytic trend has been reported for achiral phosphines [43]. Unfortunately, RuNPs were not active in the hydrogenation of the carbonyl group of acetophenone (under 40 bar H 2 at 50 • C overnight).…”
Section: Hydrogenation Reactivitysupporting
confidence: 78%
“…5%), in addition to the corresponding ethyl derivatives 5 and 6. A similar catalytic trend has been reported for achiral phosphines [43]. Unfortunately, RuNPs were not active in the hydrogenation of the carbonyl group of acetophenone (under 40 bar H 2 at 50 • C overnight).…”
Section: Hydrogenation Reactivitysupporting
confidence: 78%
“…73 Because of its nature, availability, and physico‐chemical properties, glycerol seems an appropriate choice. In the last few years, we have been interested in the synthesis of well‐defined PdNPs74 and Cu 2 ONPs75 in glycerol with the aim of applying them in different kinds of transformations (CC and Cheteroatom bond formation processes, hydrogenations, cycloadditions) and also in “one‐pot” sequential and tandem transformations, using the same catalytic precursor for multi‐step syntheses 74. 76…”
Section: Metal Nanoparticlesmentioning
confidence: 99%
“…The Pd‐based nanosystem was active for both CX (X=C, N, P) bond formation processes and hydrogenations of CC bonds of a large variety of substrates (Scheme ). This versatility permitted the employment of this type of catalyst in CC coupling followed by hydrogenation sequential processes 74. The catalyst could be recycled more than ten times without loss of activity, with negligible palladium content on the organic product (not detected by ICP‐MS).…”
Section: Metal Nanoparticlesmentioning
confidence: 99%
“…According to the pure TNT UV-Vis spectra, there is no remarkable absorption after 280 nm. [60][61][62][63] When reductant BH 4 À is added, complex products…”
Section: Catalytic Reduction Of Tntmentioning
confidence: 99%