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二茂铁基功能化二氧化硅纳米粒子:制备、表征及界面分子识别

Ferrocenyl-functionalized silica nanoparticles: preparation, characterization, and molecular recognition at interfaces.

作者信息

Ling Xing Yi, Reinhoudt David N, Huskens Jurriaan

机构信息

Laboratories of Supramolecular Chemistry & Technology and Molecular Nanofabrication, MESA+ Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE, Enschede, The Netherlands.

出版信息

Langmuir. 2006 Oct 10;22(21):8777-83. doi: 10.1021/la0610497.

Abstract

Ferrocenyl-functionalized silica nanoparticles (Fc-SiO(2), 6a-6c) of about 60 nm with supramolecular "guest" properties were prepared. Nanoparticles 6a-6c differed by the addition of different molar ratios of starting compounds during the functionalization step, i.e., 1:0, 1:10, and 1:90 of 2-ferrocenyl amidoethoxyethanol and diethylene glycol for 6a,6b, and 6c, respectively. X-ray photoelectron spectroscopy (XPS) proved the presence of ferrocenyl groups on the surfaces of 6a-6c, whereas the elemental analysis revealed an iron content of particles 6a-6c of 0.10-0.16%. Dynamic light scattering (DLS) results showed that, compared with 6a, 6b dispersed well in aqueous media, possibly due to the presence of diethylene glycol at the surfaces of 6b that significantly increases its overall hydrophilicity. Cyclic voltammetry of 6b indicated a totally irreversible system and a "mixed" diffusion-adsorption behavior, which is attributed to sluggish electron transfer. The shifted |I(p,C)/I(p,A*)| ratio showed that the ferrocenyl groups are robustly attached to the nanoparticle surface within the experimental potential range. The supramolecular recognition of Fc-SiO(2) nanoparticles at interfaces was verified by their adsorption on beta-cyclodextrin (beta-CD) self-assembled monolayers, as monitored by surface plasmon resonance (SPR) spectroscopy. The ability of the Fc-SiO(2) nanoparticles to form host-guest interactions was also demonstrated by the attachment of beta-CD-functionalized Au nanoparticles (2.8 nm) on the Fc-SiO(2) surfaces, when mixed in solution.

摘要

制备了具有超分子“客体”性质、粒径约为60 nm的二茂铁基功能化二氧化硅纳米颗粒(Fc-SiO₂,6a - 6c)。纳米颗粒6a - 6c在功能化步骤中因添加了不同摩尔比的起始化合物而有所不同,即对于6a、6b和6c,2 - 二茂铁基氨基乙氧基乙醇与二甘醇的比例分别为1:0、1:10和1:90。X射线光电子能谱(XPS)证明了6a - 6c表面存在二茂铁基,而元素分析显示颗粒6a - 6c的铁含量为0.10 - 0.16%。动态光散射(DLS)结果表明,与6a相比,6b在水性介质中分散良好,这可能是由于6b表面存在二甘醇,显著增加了其整体亲水性。6b的循环伏安法表明这是一个完全不可逆的体系以及“混合”的扩散 - 吸附行为,这归因于缓慢的电子转移。|I(p,C)/I(p,A*)|比值的变化表明,在实验电位范围内,二茂铁基牢固地附着在纳米颗粒表面。通过表面等离子体共振(SPR)光谱监测,Fc-SiO₂纳米颗粒在界面上对β - 环糊精(β - CD)自组装单分子层的吸附验证了其在界面处的超分子识别。当在溶液中混合时,Fc-SiO₂纳米颗粒表面附着β - CD功能化的金纳米颗粒(2.8 nm)也证明了其形成主客体相互作用的能力。

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