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   <dc:title>Synthesis and structural characterization of homochiral 2D coordination polymers of zinc and copper with conformationally flexible ditopic imidazolium-based dicarboxylate ligands</dc:title>
   <dc:creator>Nicasio, Antonio I.</dc:creator>
   <dc:creator>Montilla, Francisco</dc:creator>
   <dc:creator>Álvarez, Eleuterio</dc:creator>
   <dc:creator>Pérez-Colodrero, Rosario Mercedes</dc:creator>
   <dc:creator>Galindo, Agustín</dc:creator>
   <dc:subject>Química inorgánica</dc:subject>
   <dcterms:abstract>Different novel coordination polymers containing zinc, 1–4, and copper, 5–8, metals, connected via&#xd;
chiral imidazolium-based dicarboxylate ligands, [LR]−, were isolated by reaction between zinc acetate or&#xd;
copper acetate and enantiomerically pure HLR compounds. They were characterised and structurally&#xd;
identified by X-ray diffraction methods (single crystal and powder). These compounds are twodimensional&#xd;
homochiral coordination polymers, [M(LR)2]n, in which the metal ions are coordinated by the&#xd;
two carboxylate groups of [LR]− anions in a general bridging monodentate μ2–κ1-O1,κ1-O3 fashion that&#xd;
afforded tetrahedral metal coordination environments for zinc, 1–4, and square planar for copper, 5–8,&#xd;
complexes. In all the compounds the 3D supramolecular architecture is constructed by non-covalent&#xd;
interactions between the hydrophobic parts (R groups) of the homochiral 2D coordination polymers and,&#xd;
in some cases, by weak C–H⋯O non-classical hydrogen bonds that provided, in general, a dense crystal&#xd;
packing. DFT calculations on the [LR]− anions confirmed their conformational flexibility as ditopic linkers&#xd;
and this fact makes possible the formation of different coordination polymers for four-coordinated metal&#xd;
centers. Preliminary studies on the Zn-catalyzed synthesis of chiral α-aminophosphonates were carried&#xd;
out and, unfortunately, no enantioselectivity was observed in these reactions.</dcterms:abstract>
   <dcterms:dateAccepted>2021-03-04T10:43:51Z</dcterms:dateAccepted>
   <dcterms:available>2021-03-04T10:43:51Z</dcterms:available>
   <dcterms:created>2021-03-04T10:43:51Z</dcterms:created>
   <dcterms:issued>2016-11-30</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Dalton Trans., 2017, 46, 471</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/21021</dc:identifier>
   <dc:identifier>10.1039/c6dt03712g</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>The Royal Society of Chemistry</dc:publisher>
</qdc:qualifieddc>
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