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由庚胺β-环糊精介导的 CdS 纳米晶体的相转移。

Phase transfer of CdS nanocrystals mediated by heptamine β-cyclodextrin.

机构信息

IPCF-CNR Bari division, Via Orabona 4, Bari, 70126, Italy.

出版信息

Langmuir. 2012 Jun 12;28(23):8711-20. doi: 10.1021/la3007469. Epub 2012 Jun 1.

Abstract

A fundamental and systematic study on the fabrication of a supramolecularly assembled nanostructure of an organic ligand-capped CdS nanocrystal (NC) and multiple heptamine β-cyclodextrin ((NH(2))(7)βCD) molecules in aqueous solution has been here reported. The functionalization process of presynthesized hydrophobic CdS NCs by means of (NH(2))(7)βCD has been extensively investigated by using different spectroscopic and structural techniques, as a function of different experimental parameters, such as the composition and the concentration of CD, the concentration of CdS NCs, the nature of the NC surface capping ligand (oleic acid and octylamine), and the organic solvent. The formation of a complex based on the direct coordination of the (NH(2))(7)βCD amine groups at the NC surface has been demonstrated and found responsible for the CdS NC phase transfer process. The amine functional group in (NH(2))(7)βCD and the appropriate combination of pristine capping agent coordinating the NC surface and a suitable solvent have been found decisive for the success of the CdS NC phase transfer process. Furthermore, a layer-by-layer assembly experiment has indicated that the obtained (NH(2))(7)βCD functionalized CdS NCs are still able to perform the host-guest chemistry. Thus, they offer a model of a nanoparticle-based material with molecular receptors, useful for bio applications.

摘要

本文报道了在水溶液中制备有机配体封端的 CdS 纳米晶(NC)和多个庚胺 β-环糊精((NH(2))(7)βCD)分子的超分子组装纳米结构的基础和系统研究。通过使用不同的光谱和结构技术,广泛研究了通过(NH(2))(7)βCD 对预合成的疏水性 CdS NC 的功能化过程,作为不同实验参数的函数,例如 CD 的组成和浓度、CdS NC 的浓度、NC 表面封端配体的性质(油酸和辛胺)和有机溶剂。已经证明了基于 NC 表面上的(NH(2))(7)βCD 胺基团的直接配位形成的配合物,并且发现其负责 CdS NC 的相转移过程。(NH(2))(7)βCD 中的胺官能团以及与 NC 表面配位的原始封端剂和合适溶剂的适当组合被发现对 CdS NC 相转移过程的成功至关重要。此外,逐层组装实验表明,所得的(NH(2))(7)βCD 功能化的 CdS NC 仍然能够进行主体-客体化学。因此,它们提供了一种基于纳米粒子的具有分子受体的材料模型,可用于生物应用。

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