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基于实验和理论研究的多金属氧酸盐-苯丙氨酸杂化纳米球的自组装

Self-assembly study of nanometric spheres from polyoxometalate-phenylalanine hybrids, an experimental and theoretical approach.

机构信息

Department of Chemistry, University of Crete, Laboratory of BioInorg. Chem., Voutes Campus, 70013 Heraklion, Crete, Greece.

出版信息

Dalton Trans. 2018 May 8;47(18):6304-6313. doi: 10.1039/c8dt00380g.

Abstract

Herein, we report on the study of supramolecular assemblies based on polyoxometalates (POMs) upon their modification with amino acids. Two POM-amino acid hybrids were synthesized by coupling a functionalized Keggin type polyoxoanion [PW11O39{Sn(C6H4)C[triple bond, length as m-dash]C(C6H4)COOH}]4- with carboxyl-protected (methyl-ester) phenylalanine or diphenylalanine peptides. Surprisingly, all compounds, including the initial POM, formed supramolecular nanospheres in different solvent mixtures, which were examined by scanning electron microscopy (SEM). Molecular dynamics (MD) simulations for the POM-amino acid species revealed that the hydrophobic forces are mainly responsible for the initial aggregation into incipient micelle type structures, in which the organic arms are buried inside the aggregate while POM polar heads are more exposed to the solvent with tetrabutyl-ammonium counter cations acting as linkers.

摘要

在此,我们报告了基于多金属氧酸盐(POMs)的超分子组装体的研究,这些组装体通过与氨基酸进行修饰而得到。通过将功能化的 Keggin 型多氧阴离子[PW11O39{Sn(C6H4)C[三重键,长度为 m-dash]C(C6H4)COOH}]4-与羧基保护(甲酯)苯丙氨酸或二苯丙氨酸肽偶联,合成了两种 POM-氨基酸杂化物。令人惊讶的是,所有化合物,包括初始 POM,在不同的溶剂混合物中都形成了超分子纳米球,这通过扫描电子显微镜(SEM)进行了检查。对 POM-氨基酸物种的分子动力学(MD)模拟表明,疏水相互作用力主要负责最初的聚集形成初始胶束型结构,其中有机臂埋藏在聚集体内部,而 POM 极性头更多地暴露于溶剂中,四丁基铵反离子作为连接体。

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