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First enantioseparation and circular dichroismspectra of Au38 clusters protected by achiralligands

机译:非手性配体保护的Au38团簇的对映异构体和圆二色性光谱

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摘要

Bestowing chirality to metals is central in fields such as heterogeneous catalysis and modernoptics. Although the bulk phase of metals is symmetric, their surfaces can become chiralthrough adsorption of molecules. Interestingly, even achiral molecules can lead to locally chiral,though globally racemic, surfaces. A similar situation can be obtained for metal particles orclusters. Here we report the first separation of the enantiomers of a gold cluster protectedby achiral thiolates, Au38(sCH2CH2 Ph)24, achieved by chiral high-performance liquidchromatography. The chirality of the nanocluster arises from the chiral arrangement of thethiolates on its surface, forming ‘staple motifs’. The enantiomers show mirror-image circulardichroism responses and large anisotropy factors of up to 4×10~(-3). Comparison with reportedcircular dichroism spectra of other Au38 clusters reveals that the influence of the ligand on thechiroptical properties is minor.
机译:在多相催化和现代光学等领域,赋予金属手性至关重要。尽管金属的主体相是对称的,但它们的表面可通过吸附分子而变成手性。有趣的是,即使是非手性分子也可以导致局部手性的表面,尽管总体上是外消旋的。对于金属颗粒或团簇可以获得类似的情况。在这里,我们报告了通过手性高效液相色谱法实现的非手性硫醇盐保护的金簇对映体Au38(sCH2CH2 Ph)24的首次分离。纳米簇的手性来自硫醇盐在其表面上的手性排列,形成“钉书针”。对映异构体表现出镜像圆二色性反应,并且各向异性系数高达4×10〜(-3)。与报道的其他Au38团簇的圆二色性光谱比较表明,配体对手性的影响很小。

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