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通过静电和配位相互作用对富勒醇进行定向组装,以制备多种水溶性金属阳离子-富勒烯纳米簇配合物。

Directed assembly of fullerenols electrostatic and coordination interactions to fabricate diverse and water-soluble metal cation-fullerene nanocluster complexes.

作者信息

He Rui, Fan Chenjie, Liang Qingyuan, Wang Yan, Gao Yanyan, Wu Jiakai, Wu Qingnan, Tai Fuju

机构信息

NanoAgro Center, College of Plant Protection, Henan Agricultural University Zhengzhou 450046 China

National Key Laboratory of Wheat and Maize Crop Science, College of Life Science, Henan Agricultural University Zhengzhou 450046 China

出版信息

RSC Adv. 2024 Jan 3;14(2):1472-1487. doi: 10.1039/d3ra07725j. eCollection 2024 Jan 2.

DOI:10.1039/d3ra07725j
PMID:38174261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10763661/
Abstract

Metal ion-nanocluster coordination complexes can produce a variety of functional engineered nanomaterials with promising characteristics to enable widespread applications. Herein, the visualization observation of the interactions of metal ions and fullerene derivatives, particularly anionic fullerenols (Fol), were carried out in aqueous solutions. The alkali metal salts only resulted in salting out of Fol to gain re-soluble sediments, whereas multivalent metal cations (M, = 2, 3) modulated further assembly of Fol to produce insoluble hybrids. These provide crucial insights into the directed assembly of Fol that two major forces involved in actuation are electrostatic and coordination effects. Through the precise modulation of feed ratios of Fol to M, a variety of water-soluble M@Fol coordination complexes were facilely prepared and subsequently characterized by various measurements. Among them, X-ray photoelectron spectra validated the coordination effects through the metal cation and oxygen binding feature. Transmission electron microscopy delivered valuable information about diverse morphologies and locally-ordered microstructures at the nanoscale. This study opens a new opportunity for developing a preparation strategy to fabricate water-soluble metal cation-fullerenol coordination complexes with various merits for potential application in biomedical fields.

摘要

金属离子 - 纳米团簇配位络合物可以制备出具有多种有前景特性的功能性工程纳米材料,从而实现广泛应用。在此,对金属离子与富勒烯衍生物,特别是阴离子型富勒醇(Fol)在水溶液中的相互作用进行了可视化观察。碱金属盐只会导致Fol盐析,得到可再溶解的沉淀物,而多价金属阳离子(M,n = 2, 3)则会调节Fol的进一步组装,生成不溶性杂化物。这些结果为Fol的定向组装提供了关键见解,即驱动过程中涉及的两种主要作用力是静电作用和配位作用。通过精确调节Fol与M的进料比例,轻松制备了多种水溶性M@Fol配位络合物,随后通过各种测量对其进行了表征。其中,X射线光电子能谱通过金属阳离子与氧的结合特征验证了配位作用。透射电子显微镜提供了有关纳米级各种形态和局部有序微观结构的有价值信息。本研究为开发一种制备策略提供了新机会,以制造具有各种优点的水溶性金属阳离子 - 富勒醇配位络合物,用于生物医学领域的潜在应用。

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