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Surface Functionalization of Metal-Organic Frameworks for Improved Moisture Resistance
Published on: September 5, 2018
Investigation of layered double hydroxides intercalated by oxomolybdenum catecholate complexes
Bernardo Monteiro1, Sandra Gago, Filipe A Almeida Paz
1Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal.
Oxomolybdenum(VI) complexes were successfully incorporated into layered double hydroxides (LDHs) using ion exchange. Spectroscopic and diffraction analyses confirmed the intercalation of binuclear complexes within the LDH structure.
Area of Science:
- Materials Science
- Inorganic Chemistry
- Nanotechnology
Background:
- Layered double hydroxides (LDHs) are versatile materials with tunable properties.
- Molybdenum complexes offer unique functionalities for material applications.
Purpose of the Study:
- To incorporate oxomolybdenum(VI) complexes of 3,4-dihydroxybenzoic acid into various LDH precursors.
- To characterize the resulting intercalated materials and understand the complex's behavior within the LDH structure.
Main Methods:
- Ion exchange reactions using LDH-nitrate (Zn-Al, Mg-Al) and LDH-chloride (Li-Al) precursors.
- Characterization techniques including elemental analysis, SEM-EDS, Mo K-edge EXAFS, IR, Raman, UV-vis, NMR, and XRPD.
Main Results:
- Successful ion exchange achieved, replacing over 90% of interlayer anions.
- Formation of expanded LDHs with basal spacing around 15.4 Å.
- Spectroscopic and diffraction data confirmed the intercalation of mono- and binuclear molybdenum complexes, with binuclear species dominating in certain preparations.
Conclusions:
- Oxomolybdenum(VI) complexes can be effectively intercalated into LDHs.
- The orientation and proportion of intercalated complexes depend on the LDH support and reaction conditions.
- The study provides insights into the structural arrangement of guest complexes within LDH interlayers.
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