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通过顺序封装-结晶法将功能性纳米颗粒限制在基于胶体亚胺的共价有机框架球体中。

Confining Functional Nanoparticles into Colloidal Imine-Based COF Spheres by a Sequential Encapsulation-Crystallization Method.

作者信息

Rodríguez-San-Miguel David, Yazdi Amirali, Guillerm Vincent, Pérez-Carvajal Javier, Puntes Víctor, Maspoch Daniel, Zamora Félix

机构信息

Departamento de Química Inorgánica and Institute for Advanced Research in Chemical Sciences, Universidad Autónoma de Madrid, 28049, Madrid, Spain.

Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and The Barcelona Institute of Science and Technology, Campus UAB, Bellaterra, 08193, Barcelona, Spain.

出版信息

Chemistry. 2017 Jun 27;23(36):8623-8627. doi: 10.1002/chem.201702072. Epub 2017 Jun 13.

Abstract

Here, a two-step method is reported that enables imparting new functionalities to covalent organic frameworks (COFs) by nanoparticle confinement. The direct reaction between 1,3,5-tris(4-aminophenyl)benzene and 1,3,5-benzenetricarbaldehyde in the presence of a variety of metallic/metal-oxide nanoparticles resulted in embedding of the nanoparticles in amorphous and non-porous imine-linked polymer organic spheres (NP@a-1). Post-treatment reactions of NP@a-1 with acetic acid under reflux led to crystalline and porous imine-based COF-hybrid spheres (NP@c-1). Interestingly, Au@c-1 and Pd@c-1 were found to be catalytically active.

摘要

本文报道了一种两步法,该方法能够通过纳米颗粒限域作用赋予共价有机框架(COF)新的功能。在多种金属/金属氧化物纳米颗粒存在的情况下,1,3,5-三(4-氨基苯基)苯与1,3,5-苯三甲醛之间的直接反应导致纳米颗粒嵌入无定形且无孔的亚胺连接的聚合物有机球体(NP@a-1)中。NP@a-1与乙酸在回流条件下进行后处理反应,得到结晶且多孔的亚胺基COF杂化球体(NP@c-1)。有趣的是,发现Au@c-1和Pd@c-1具有催化活性。

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