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扭曲和螺旋纳米无定形二氧化硅中硅氧烷手性的直接观察。

Direct Observation of Siloxane Chirality on Twisted and Helical Nanometric Amorphous Silica.

机构信息

Department of Applied Chemistry and Biochemistry, Kumamoto University , 2-39-1 Kurokami, Chuo-ku Kumamoto 860-8555, Japan.

Institut des Sciences Moléculaires, (UMR5255 ISM), CNRS, University of Bordeaux , 33405 Talence, France.

出版信息

Nano Lett. 2016 Oct 12;16(10):6411-6415. doi: 10.1021/acs.nanolett.6b02858. Epub 2016 Sep 6.

Abstract

Synthesis of chiral inorganic or hybrid nanomaterials through sol-gel transcription of chiral organic templates has attracted a great deal of interest for more than a decade. However, the chiral nature of these inorganic matrices has never been directly observed. For the first time, we report a direct evaluation of chirality on noncrystalline silica chiral nanoribbons by vibrational circular dichroism (VCD) measurements. Strong Cotton effect around 1150-1000 cm from Si-O-Si asymmetric stretching vibration was observed. Surprisingly, calcination of these hybrid nanoribbons doubled the intensity of Cotton effects. On the basis of transmission electron microscopy observations, IR, VCD, NMR, and Raman spectroscopies, we demonstrate that the silica chirality originates from twisted siloxane network composed of chiral arrangement of the Si-O-Si bonds. Our findings clearly prove the presence of chiral organization of amorphous silica network, making them very promising chiral platforms for chiral recognition, optical applications, or asymmetric catalysis.

摘要

通过手性有机模板的溶胶-凝胶转录合成手性无机或杂化纳米材料在十多年来引起了极大的兴趣。然而,这些无机基质的手性性质从未被直接观察到。我们首次通过振动圆二色性(VCD)测量报告了非晶态硅手性纳米带的手性的直接评估。在 Si-O-Si 不对称伸缩振动周围约 1150-1000 cm 处观察到强的Cotton 效应。令人惊讶的是,这些杂化纳米带的煅烧使 Cotton 效应的强度增加了一倍。基于透射电子显微镜观察、IR、VCD、NMR 和拉曼光谱,我们证明了硅石的手性源于由 Si-O-Si 键的手性排列组成的扭曲的硅氧烷网络。我们的发现清楚地证明了无定形硅网络的手性组织的存在,使它们成为非常有前途的手性识别、光学应用或不对称催化的手性平台。

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