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Single- and multi-component chiral supraparticles as modular enantioselective catalysts

机译:单组分和多组分手性超微粒作为模块化对映选择性催化剂

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摘要

Nanoscale biological assemblies exemplified by exosomes, endosomes and capsids, play crucial roles in all living systems. Supraparticles (SP) from inorganic nanoparticles (NPs) replicate structural characteristics of these bioassemblies, but it is unknown whether they can mimic their biochemical functions. Here, we show that chiral ZnS NPs self-assemble into 70–100 nm SPs that display sub-nanoscale porosity associated with interstitial spaces between constituent NPs. Similarly to photosynthetic bacterial organelles, these SPs can serve as photocatalysts, enantioselectively converting L- or D-tyrosine (Tyr) into dityrosine (diTyr). Experimental data and molecular dynamic simulations indicate that the chiral bias of the photocatalytic reaction is associated with the chiral environment of interstitial spaces and preferential partitioning of enantiomers into SPs, which can be further enhanced by co-assembling ZnS with Au NPs. Besides replicating a specific function of biological nanoassemblies, these findings establish a path to enantioselective oxidative coupling of phenols for biomedical and other needs.
机译:以外泌体,内体和衣壳为例的纳米级生物组装在所有生命系统中都起着至关重要的作用。来自无机纳米颗粒(NPs)的超颗粒(SP)复制了这些生物组件的结构特征,但尚不清楚它们是否可以模仿其生物化学功能。在这里,我们表明手性ZnS NPs自组装成70–100 nm SP,显示与组成NP之间的间隙相关的亚纳米级孔隙。与光合细菌细胞器相似,这些SP可以用作光催化剂,将L-或D-酪氨酸(Tyr)对映选择性地转化为二酪氨酸(diTyr)。实验数据和分子动力学模拟表明,光催化反应的手征性与间隙空间的手性环境以及对映异构体优先分配到SP中有关,这可以通过将ZnS与Au NPs共组装来进一步增强。除了复制生物纳米组件的特定功能外,这些发现还为生物医学和其他需求建立了酚的对映选择性氧化偶联途径。

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