Stabilisation of water-soluble platinum nanoparticles by phosphonic acid derivatives

被引:8
|
作者
Richter, Mareike [1 ]
Karschin, Arndt [1 ]
Spingler, Bernhard [2 ]
Kunz, Peter C. [1 ]
Meyer-Zaika, Wolfgang [3 ]
Klaeui, Wolfgang [1 ]
机构
[1] Univ Dusseldorf, Lehrstuhl Bioanorgan Chem & Katalyse 1, Inst Anorgan Chem & Strukturchem, D-40225 Dusseldorf, Germany
[2] Univ Zurich, Inst Anorgan Chem, CH-8057 Zurich, Switzerland
[3] Univ Duisburg Essen, Inst Anorgan Chem, D-45117 Essen, Germany
关键词
METAL NANOPARTICLES; HYDROGENATION; NANOCLUSTERS; SIZE; MECHANISM; CATALYSTS; REDUCTION; COLLOIDS; RHODIUM;
D O I
10.1039/c2dt12071b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Sodium 2-(diphenylphosphino)ethyl phosphonate (1) was investigated as a stabilising agent for platinum nanoparticles (Pt-NPs) in aqueous solution. This phosphino phosphonate is known to stabilise rhodium nanoparticles (NPs) in water. Here we report that in the case of Pt-NPs this ligand is indirectly involved in the stabilisation mechanism and the actual stabilisation agent is the platinum complex Na-2[Pt(1)(2)] (2). The reduction of platinum(II) salts in the presence of the phosphonates 1, 2, sodium 2-(diphenylphosphoryl)ethyl phosphonate (3) and 3,3,3-triphenylpropyl phosphonate (4) leads to stable platinum NPs with a remarkably narrow particle size distribution. These platinum NPs show high catalytic activity in the hydrogenation of 1-hexene and 1-chloro-3-nitrobenzene under biphasic as well as heterogeneous (supported on charcoal) conditions. The activity of the supported NPs was 30 times higher than the commercially available catalyst Pt(0) EnCat (R). Furthermore, the single-crystal X-ray structures of (1)(MeOH)(2)(H2O)(2), (3)(H2O)(4), and (4) 2(H2O)(17) have been determined.
引用
收藏
页码:3407 / 3413
页数:7
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