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Enantioselective control of lattice and shape chirality in inorganic nanostructures using chiral biomolecules

机译:使用手性生物分子对无机纳米结构的晶格和形状手性进行对映选择性控制

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摘要

A large number of inorganic materials form crystals with chiral symmetry groups. Enantioselectively synthesizing nanostructures of such materials should lead to interesting optical activity effects. Here we report the synthesis of colloidal tellurium and selenium nanostructures using thiolated chiral biomolecules. The synthesis conditions are tuned to obtain tellurium nanostructures with chiral shapes and large optical activity. These nanostructures exhibit visible optical and chiroptical responses that shift with size and are successfully simulated by an electromagnetic model. The model shows that they behave as chiral optical resonators. The chiral tellurium nanostructures are transformed into chiral gold and silver telluride nanostructures with very large chiroptical activity, demonstrating a simple colloidal chemistry path to chiral plasmonic and semiconductor metamaterials. These materials are natural candidates for studies related to interactions of chiral (bio)molecules with chiral inorganic surfaces, with relevance to asymmetric catalysis, chiral crystallization and the evolution of homochirality in biomolecules.
机译:大量的无机材料形成具有手性对称基团的晶体。对映选择性地合成这种材料的纳米结构将导致有趣的光学活性效应。在这里,我们报告使用硫醇化的手性生物分子合成胶态碲和硒纳米结构。调节合成条件以获得具有手性形状和大光学活性的碲纳米结构。这些纳米结构表现出可见的光学和手性响应,并随尺寸变化,并已通过电磁模型成功模拟。该模型显示它们的行为就像手性光学谐振器。手性碲纳米结构被转变为具有非常大的手性活性的手性金和银碲化物纳米结构,这说明了手性等离子体和半导体超材料的简单胶体化学路径。这些材料是用于研究手性(生物)分子与手性无机表面相互作用的自然候选者,与不对称催化,手性结晶和生物分子中同手性的演化有关。

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