2005
DOI: 10.1246/cl.2005.1262
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A New Straightforward and Mild Preparation of Nickel(0) Nanoparticles

Abstract: Very fine nickel nanoparticles with diameters of 2.5 ± 1.5 nm have been prepared by reduction of anhydrous nickel(II) chloride with lithium powder and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB) in THF at room temperature.

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Cited by 40 publications
(15 citation statements)
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“…Among these oxides, nickel was present as NiO, so that a reduction to Ni(0) was required. Production of Ni(0) nanoparticles used as catalyst for H-transfer hydrogenation has been previously performed by reduction of Ni(II) salts with several reducing agents, such as metal lithium [31][32][33][34][35], hydrazine [36][37][38][39][40], NaBH 4 [41][42][43], ethylene glycol [44][45][46], oleylamine/trioctylphosphine [47] or by thermal decomposition of nickel isopropoxide, prepared with an excess of Li, Na or K metal [48]. In spite of their efficiency, these reducing agents are toxic or hazardous to manipulate.…”
Section: Resultsmentioning
confidence: 99%
“…Among these oxides, nickel was present as NiO, so that a reduction to Ni(0) was required. Production of Ni(0) nanoparticles used as catalyst for H-transfer hydrogenation has been previously performed by reduction of Ni(II) salts with several reducing agents, such as metal lithium [31][32][33][34][35], hydrazine [36][37][38][39][40], NaBH 4 [41][42][43], ethylene glycol [44][45][46], oleylamine/trioctylphosphine [47] or by thermal decomposition of nickel isopropoxide, prepared with an excess of Li, Na or K metal [48]. In spite of their efficiency, these reducing agents are toxic or hazardous to manipulate.…”
Section: Resultsmentioning
confidence: 99%
“…The practical benefit of this synthesis is controllability of the size. Synthesis of monodispersed nanoclusters of Pd [14][15][16], Pt [17,18], Rh [19,20], Au [21,22] and Ni [23,24] has been reported.…”
Section: Introductionmentioning
confidence: 99%
“…6 The high reactivity of these nanoparticles was demonstrated in the catalytic hydrogenation and reduction of a variety of organic compounds, including carbon-carbon multiple-bond-containing compounds. In particular, the two latter systems have found application in the highly selective conjugate reduction of α,β-unsaturated carbonyl compounds 10 as well as in the stereoselective cis semihydrogenation of internal alkynes and the semihydrogenation of terminal alkynes under mild reaction conditions.…”
Section: Introductionmentioning
confidence: 99%