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首页> 外文期刊>Journal of Molecular Liquids >Interaction of M@Au-12 nanocluster (M = Au, Ag, Pd, and Pt) with different forms of cysteine (uncharged, cationic, anionic, and zwitterion) via the Au-S bond
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Interaction of M@Au-12 nanocluster (M = Au, Ag, Pd, and Pt) with different forms of cysteine (uncharged, cationic, anionic, and zwitterion) via the Au-S bond

机译:M @ AU-12纳米簇(M = Au,Ag,Pd和Pt)的相互作用通过AU-S键具有不同形式的半胱氨酸(不带电,阳离子,阴离子和两倍)

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摘要

In this work, the effect of the type of core-metal (M = Au, Ag, Pd, and Pt) of a M@Au-12 nanocluster on its interaction with the different forms of cysteine (CYS) (uncharged, anionic, cationic, and zwitterion) via the formation of Au-S bond is investigated. Other issues considered in this investigation are the adsorption energy and adsorption mode, the strength of the Au-S bond, and the IR spectrum of the considered forms of CYS. Also, the effect of the type of M on the combination of the frontier molecular orbitals of the considered CYS forms with the molecular orbitals of metal nanoclusters is investigated. The interaction of the CYS, in its zwitterion form, with the considered nanoclusters, is studied in the microhydration, water considering the polarized continuum model (PCM), and PCM + microhydration environments, separately. The selected metal nanoclusters can be considered as small models of the core-shell nanoparticles to see how the type of core-metal atoms influences the interaction of different forms of CYS with the core-shell nanoparticles. (C) 2021 Elsevier B.V. All rights reserved.
机译:在这项工作中,研究了a的核心金属类型(M=Au、Ag、Pd和Pt)的影响M@Au-研究了12纳米团簇通过形成Au-S键与不同形式的半胱氨酸(CYS)(不带电、阴离子、阳离子和两性离子)的相互作用。本研究中考虑的其他问题包括吸附能量和吸附模式、Au-S键的强度以及所考虑的CYS形式的红外光谱。此外,还研究了M类型对所考虑的CYS形式的前线分子轨道与金属纳米团簇的分子轨道组合的影响。在微水化、考虑极化连续介质模型(PCM)的水和PCM+微水化环境中,分别研究了两性离子形式的CYS与所考虑的纳米团簇的相互作用。选定的金属纳米团簇可被视为核壳纳米颗粒的小模型,以了解核金属原子的类型如何影响不同形式的CYS与核壳纳米颗粒的相互作用。(c)2021爱思唯尔B.V.保留所有权利。

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