6533b85dfe1ef96bd12bde42
RESEARCH PRODUCT
Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal–Organic Framework
Emilio PardoDonatella ArmentanoJorge GasconFrancisco R. Fortea-pérezAntonio Leyva-pérezMarta MonThais GranchaJesús Ferrando-soriasubject
chemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesBiochemistrySulfurCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryThioetherchemistryvisual_artvisual_art.visual_art_mediumOrganic chemistryMetal-organic framework0210 nano-technologyHybrid materialHydroalkoxylationdescription
A novel chiral 3D bioMOF exhibiting functional channels with thio-alkyl chains derived from the natural amino acid l-methionine (1) has been rationally prepared. The well-known strong affinity of gold for sulfur derivatives, together with the extremely high flexibility of the thioether "arms" decorating the channels, account for a selective capture of gold(III) and gold(I) salts in the presence of other metal cations typically found in electronic wastes. The X-ray single-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the selective metal capture occurs in a metal ion recognition process somehow mimicking what happens in biological systems and protein receptors. Both Au(III)@1 and Au(I)@1 display high activity as heterogeneous catalyst for the hydroalkoxylation of alkynes, further expanding the application of these novel hybrid materials.
year | journal | country | edition | language |
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2016-06-16 | Journal of the American Chemical Society |