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金@苯乙炔有机金簇:金-碳共价键的直接光谱证据。

Au@Phenyacetylene organogold clusters: direct spectroscopic evidence of gold-carbon covalent band.

作者信息

Zhang Hongyan, Yin Penggang, You Tingting, Sun Tianyu, Lang Xiufeng, Tan Enzhong, Liang Xiu, Guo Lin

机构信息

Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of Education, School of Chemistry and Environment, Beihang University, Beijing 100191, PR China.

Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of Education, School of Chemistry and Environment, Beihang University, Beijing 100191, PR China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Jan 5;134:96-100. doi: 10.1016/j.saa.2014.06.085. Epub 2014 Jun 23.

Abstract

Surface-enhanced Raman Scattering (SERS) as a powerful vibrational spectroscope technique is used to investigate the existence of AuC band between gold nanoparticles (AuNPs) and phenylacetylene (PA) which is characterized by a new Raman-active peak at 405 cm(-1). The measurements with transmission electron microscopy (TEM) and extinction spectroscopy show an increasing in size and spectral redshift for AuNPs after the addition of the PA molecule demonstrating the production of gold-PA organogold cluster (Au:C₂Ph). Furthermore, a strong band characteristic of AuC stretch mode is observed in the SERS spectra of Au:C₂Ph and supported by the density functional theory (DFT) calculation. In addition, the optimal adsorption of PA on AuNPs' surface is also investigated theoretically. These findings show a direct spectroscopic sight into AuC band, and offer promising alternative to thiol compounds for anchoring organic molecules to gold surface to form self-assembled monolayers.

摘要

表面增强拉曼散射(SERS)作为一种强大的振动光谱技术,用于研究金纳米颗粒(AuNPs)与苯乙炔(PA)之间AuC带的存在,其特征是在405 cm⁻¹处有一个新的拉曼活性峰。透射电子显微镜(TEM)和消光光谱测量表明,添加PA分子后AuNPs的尺寸增大且光谱发生红移,这证明了金 - PA有机金簇(Au:C₂Ph)的生成。此外,在Au:C₂Ph的SERS光谱中观察到了AuC拉伸模式的强特征峰,并且得到了密度泛函理论(DFT)计算的支持。另外,还从理论上研究了PA在AuNPs表面的最佳吸附情况。这些发现为AuC带提供了直接的光谱视角,并为硫醇化合物提供了一种有前景的替代方法,用于将有机分子锚定到金表面以形成自组装单分子层。

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