Covalent modification of surfaces with porous metal-organic materials

被引:2
|
作者
Montone, Christine M. [1 ,2 ]
Dworzak, Michael R. [2 ]
Yap, Glenn P. A. [2 ]
Bloch, Eric D. [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
基金
美国国家科学基金会;
关键词
FRAMEWORK; DEPOSITION; ADSORPTION;
D O I
10.1039/d3ta04662a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recent advances in metal-organic frameworks (MOFs) and porous coordination cages (PCCs) have led to their extensive use in various applications due to their tunable properties and exceptional surface areas. To address challenges in harnessing their tunability, surface deposition of MOFs and cages has been investigated. This paper presents efforts in surface attachment of MOFs and porous cages, leveraging click chemistry, alkylation reactions, and electrostatic approaches. HKUST-1 MOF nanoparticles were covalently tethered to an azide-modified gold surface using copper-catalyzed click chemistry, allowing precise control over the deposited layer. Calixarene and zirconium cages were also attached via click chemistry, providing controlled crystallinity and thickness. Complementary strategies using minimally-functionalized ligands enabled cage attachment to surfaces. These surface-attached porous materials offer versatile approaches for functionalizing surfaces in catalysis, sensing, drug delivery, and other applications, expanding the utility of porous materials in diverse fields. The results demonstrate the feasibility of surface attachment for porous cages. Enhancing MOF and PCC tunability: surface attachment explored via click chemistry, alkylation, and electrostatic methods.
引用
收藏
页码:23888 / 23894
页数:7
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