Covalent modification of surfaces with porous metal-organic materials
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 ha...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 11; no. 44; pp. 23888 - 23894 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
14.11.2023
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Subjects | |
Online Access | Get full text |
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Summary: | 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
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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
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click chemistry, alkylation, and electrostatic methods. |
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Bibliography: | For ESI and crystallographic data in CIF or other electronic format see DOI 2251522 Eric D. Bloch was born in Brownsville, Wisconsin, USA, in 1983. After attending The University of Wisconsin-Fond du Lac for two years, he received his B.S. in Chemistry from UW-Milwaukee in 2008 and Ph.D. in Chemistry from The University of California-Berkeley in 2014. Following postdoctoral work at Harvard University, he joined the faculty at the University of Delaware in 2016. He moved to Indiana University in 2023 where he is currently the Veronica Siedle Associate Professor in the Chemistry Department. His research involves the design, synthesis, and characterization of porous molecular materials and porous salts for applications ranging from energy storage to human health. 2251521 https://doi.org/10.1039/d3ta04662a Electronic supplementary information (ESI) available: adsorption isotherms, crystallographic information, spectroscopic data. CCDC and |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta04662a |