Department of Chemistry, University of Massachusetts, Amherst, MA 01003-9336 (USA).
College of Materials, Xiamen University, Xiamen, 361005 (P.R. China).
Angew Chem Int Ed Engl. 2015 Oct 26;54(44):12991-5. doi: 10.1002/anie.201505242. Epub 2015 Sep 9.
The use of reversible linkers in polymers has been of interest mainly for biomedical applications. Herein, we present a novel strategy to utilize reversible interactions in polymeric nanoparticles to generate hollow metal-organic nanoparticles (MOPs). These hollow MOPs are synthesized from self-assembled polymeric nanoparticles using a simple metal-comonomer exchange process in a single step. The control over the size of the polymer precursor particles translates into a straightforward opportunity for controlling MOP sizes. The shell thickness of the MOPs could be easily tuned by the concentration of metal ions in solution. The underlying mechanism for the formation of these hollow MOPs has been proposed. Evidence for the generality of the method is provided by its application to a variety of metal ions with different coordination geometries.
在聚合物中使用可逆连接体主要引起了生物医学应用的兴趣。在此,我们提出了一种新策略,即在聚合物纳米粒子中利用可逆相互作用来生成中空金属有机纳米粒子(MOPs)。这些中空 MOPs 是通过在一步中使用简单的金属-共聚单体交换过程从自组装聚合物纳米粒子合成的。对聚合物前体颗粒尺寸的控制转化为控制 MOP 尺寸的直接机会。MOP 的壳层厚度可以通过溶液中金属离子的浓度轻松调节。已经提出了形成这些中空 MOP 的基本机制。该方法的通用性已通过其在各种具有不同配位几何形状的金属离子中的应用得到证明。