Dendrimer–cyclodextrin assemblies as stabilizers for gold and platinum nanoparticles

J. Michels, J. Huskens, D. Reinhoudt
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引用次数: 5

Abstract

Aqueous assemblies of adamantyl-derivatized poly(propylene imine) (PPI) dendrimers and B-cyclodextrin (B-CD) have been used as nanoreactors in the preparation of gold and platinum nanoparticles in water. These particles have been formed by the reduction of aurate or platinate anions in the presence of the generation 4 (4·(B-CD)32) and 5 ( 5·(B-CD)40) assemblies. Lower generation assemblies did not provide stable nanoparticles. A kinetic model is proposed in which the particles form inside the dendrimer assemblies owing to preferred nucleation as a result of the electrostatic attraction between the polycationic core and the metallate anions. The persistent shape of the adamantyl-derivatized dendrimers and the dense shell of adamantyl-B-CD complexes provide a kinetic barrier for nanoparticle escape thus prolonging their lifetime. Exchange of the dendrimers for a cationic disulfide provided stable, water-soluble metal nanoparticles without change of their size distribution.
树状聚合物-环糊精组合物作为金和铂纳米颗粒的稳定剂
以金刚烷基衍生化聚丙烯亚胺(PPI)树状大分子和b -环糊精(B-CD)为纳米反应器,在水中制备了金和铂纳米粒子。这些粒子是在第4代(4·(B-CD)32)和第5代(5·(B-CD)40)离子存在下由金酸盐或铂酸盐阴离子还原而成的。较低一代的组件不能提供稳定的纳米颗粒。提出了一种动力学模型,其中由于多阳离子核和金属阴离子之间的静电吸引而形成的优先成核,粒子在树状大分子内形成。金刚烷基衍生的树状大分子的持久形状和金刚烷基- b - cd络合物的致密外壳为纳米颗粒的逃逸提供了动力学屏障,从而延长了它们的寿命。将树状大分子交换为阳离子二硫化物提供了稳定的水溶性金属纳米颗粒,而不改变其尺寸分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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