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通过金属配位进行的不连续颗粒自组装。

Patchy particle self-assembly via metal coordination.

机构信息

Molecular Design Institute and Department of Chemistry, New York University , New York, New York 10003, United States.

出版信息

J Am Chem Soc. 2013 Sep 25;135(38):14064-7. doi: 10.1021/ja4075979. Epub 2013 Sep 17.

Abstract

Colloids with high-symmetry patches are functionalized with metal-coordination-based recognition units and assembled into larger chain architectures, demonstrating for the first time the use of metal coordination as a specific force in colloidal self-assembly. The cross-linked poly(styrene)-based patchy particles are fabricated by encapsulation of colloidal clusters following a two-stage swelling and polymerization methodology. The particle patches, containing carboxylic acid groups, are site-specifically functionalized either with a triblock copolymer (TBC), bearing primary alcohols, alkyl chains, and palladated pincer receptors, synthesized by ring-opening metathesis polymerization, or with a small molecule bearing a pyridine headgroup. Functionalizing with a TBC provides design flexibility for independently setting the range of the interaction and the recognition motif.

摘要

具有高对称性补丁的胶体用基于金属配位的识别单元功能化,并组装成更大的链状结构,首次证明了金属配位作为胶体自组装中的一种特定力的应用。基于交联聚苯乙烯的有补丁的胶体颗粒是通过在两步溶胀和聚合方法之后包封胶体簇来制备的。颗粒补丁含有羧酸基团,通过开环复分解聚合合成的带有伯醇、烷基链和钯配合物夹持受体的三嵌段共聚物(TBC)或带有吡啶头基的小分子,实现了点位特异性功能化。用 TBC 进行功能化提供了设计灵活性,可以独立设置相互作用的范围和识别基序。

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