Growth of Au-Pd2Sn Nanorods via Galvanic Replacement and Their Catalytic Performance on Hydrogenation and Sonogashira Coupling Reactions

Colloidal Pd2Sn and Au-Pd2Sn nanorods (NRs) with tuned size were produced by the reduction of Pd and Sn salts in the presence of size- and shape-controlling agents and the posterior growth of Au tips through a galvanic replacement reaction. Pd2Sn and Au-Pd2Sn NRs exhibited high catalytic activity to...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 34(2018), 36 vom: 11. Sept., Seite 10634-10643
1. Verfasser: Nafria, Raquel (VerfasserIn)
Weitere Verfasser: Luo, Zhishan, Ibáñez, Maria, Martí-Sànchez, Sara, Yu, Xiaoting, de la Mata, Maria, Llorca, Jordi, Arbiol, Jordi, Kovalenko, Maksym V, Grabulosa, Arnald, Muller, Guillermo, Cabot, Andreu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't
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520 |a Colloidal Pd2Sn and Au-Pd2Sn nanorods (NRs) with tuned size were produced by the reduction of Pd and Sn salts in the presence of size- and shape-controlling agents and the posterior growth of Au tips through a galvanic replacement reaction. Pd2Sn and Au-Pd2Sn NRs exhibited high catalytic activity toward quasi-homogeneous hydrogenation of alkenes (styrene and 1-octene) and alkynes (phenylacetylene and 1-octyne) in dichloromethane. Au-Pd2Sn NRs showed higher activity than Pd2Sn for 1-octene, 1-octyne, and phenylacetylene. In Au-Pd2Sn heterostructures, X-ray photoelectron spectroscopy evidenced an electron donation from the Pd2Sn NR to the Au tips. Such heterostructures showed distinct catalytic behavior in the hydrogenation of compounds containing a triple bond such as tolan. This can be explained by the aurophilicity of triple bonds. To further study this effect, Pd2Sn and Au-Pd2Sn NRs were also tested in the Sonogashira coupling reaction between iodobenzene and phenylacetylene in N, N-dimethylformamide. At low concentration, this reaction provided the expected product, tolan. However, at high concentration, more reduced products such as stilbene and 1,2-diphenylethane were also obtained, even without the addition of H2. A mechanism for this unexpected reduction is proposed 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
700 1 |a Luo, Zhishan  |e verfasserin  |4 aut 
700 1 |a Ibáñez, Maria  |e verfasserin  |4 aut 
700 1 |a Martí-Sànchez, Sara  |e verfasserin  |4 aut 
700 1 |a Yu, Xiaoting  |e verfasserin  |4 aut 
700 1 |a de la Mata, Maria  |e verfasserin  |4 aut 
700 1 |a Llorca, Jordi  |e verfasserin  |4 aut 
700 1 |a Arbiol, Jordi  |e verfasserin  |4 aut 
700 1 |a Kovalenko, Maksym V  |e verfasserin  |4 aut 
700 1 |a Grabulosa, Arnald  |e verfasserin  |4 aut 
700 1 |a Muller, Guillermo  |e verfasserin  |4 aut 
700 1 |a Cabot, Andreu  |e verfasserin  |4 aut 
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