TY - JOUR
T1 - Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal-Organic Framework
AU - Mon, Marta
AU - Ferrando-Soria, Jesús
AU - Grancha, Thais
AU - Fortea-Pérez, Francisco R.
AU - Gascon, Jorge
AU - Leyva-Pérez, Antonio
AU - Armentano, Donatella
AU - Pardo, Emilio
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/6/29
Y1 - 2016/6/29
N2 - 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 AuIII@1 and AuI@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 AuIII@1 and AuI@1 display high activity as heterogeneous catalyst for the hydroalkoxylation of alkynes, further expanding the application of these novel hybrid materials.
AB - 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 AuIII@1 and AuI@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 AuIII@1 and AuI@1 display high activity as heterogeneous catalyst for the hydroalkoxylation of alkynes, further expanding the application of these novel hybrid materials.
UR - http://www.scopus.com/inward/record.url?scp=84976568705&partnerID=8YFLogxK
U2 - 10.1021/jacs.6b04635
DO - 10.1021/jacs.6b04635
M3 - Article
C2 - 27295383
AN - SCOPUS:84976568705
SN - 0002-7863
VL - 138
SP - 7864
EP - 7867
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 25
ER -