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Ligand effects in catalysis by atomically precise gold nanoclusters

机译:原子精确的金纳米团簇在催化中的配体效应

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摘要

Atomically precise gold nanoclusters are ideal model catalysts with well-defined compositions and tunable structures. Determination of the ligand effect on catalysis requires the use of gold nanoclusters with protecting ligands as the only variable. Two isostructural Au38 nanoclusters, [Au38(L)20(Ph3P)4]2+ (L = alkynyl or thiolate), have been synthesized by a direct reduction method, and they have an unprecedented face-centered cubic (fcc)–type Au34 kernel surrounded by 4 AuL2 staple motifs, 4 Ph3P, and 12 bridging L ligands. The Au34 kernel can be derived from the fusion of two fcc-type Au20 via sharing a Au6 face. Catalytic performance was studied with these two nanoclusters supported on TiO2 (1/TiO2 and 2/TiO2) as catalysts. The alkynyl-protected Au38 are very active (>97%) in the semihydrogenation of alkynes (including terminal and internal ones) to alkenes, whereas the thiolated Au38 showed a very low conversion (<2%). This fact suggests that the protecting ligands play an important role in H2 activation. This work presents a clear demonstration that catalytic performance of gold nanoclusters can be modulated by the controlled construction of ligand spheres.
机译:原子精确的金纳米团簇是具有明确定义的组成和可调结构的理想模型催化剂。要确定配体对催化的作用,需要使用带有保护性配体作为唯一变量的金纳米簇。通过直接还原法合成了两个同构的Au38纳米簇[Au38(L)20(Ph3P)4] sup> 2 + (L =炔基或硫醇盐),它们具有前所未有的面心立方(fcc)型Au34内核,周围有4个AuL2钉基序,4个Ph3P和12个桥接L配体。 Au34内核可以通过共享一个Au6面从两个fcc型Au20的融合中获得。用TiO2(1 / TiO2和2 / TiO2)担载的这两个纳米团簇作为催化剂研究了催化性能。炔基保护的Au38在炔烃(包括末端和内部的炔烃)的半氢化反应中非常活跃(> 97%),而硫醇化的Au38却显示出非常低的转化率(<2%)。这一事实表明保护配体在H 2 活化中起重要作用。这项工作清楚地证明了金纳米团簇的催化性能可以通过配体球的受控结构来调节。

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