<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(19)</volume><submitter>Kang X</submitter><pubmed_abstract>Three new products, [Cu&lt;sub>2&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>3&lt;/sub>&lt;i>-&lt;/i>dppa)(2,2'-bipy)&lt;sub>2&lt;/sub>(H&lt;sub>2&lt;/sub>O)]&lt;i>&lt;sub>n&lt;/sub>&lt;/i>·2&lt;i>n&lt;/i>H&lt;sub>2&lt;/sub>O (&lt;b>1&lt;/b>), [Co&lt;sub>4&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>4&lt;/sub>&lt;i>-&lt;/i>dppa)&lt;sub>2&lt;/sub>(phen)&lt;sub>4&lt;/sub>(H&lt;sub>2&lt;/sub>O)&lt;sub>4&lt;/sub>]·2H&lt;sub>2&lt;/sub>O (&lt;b>2&lt;/b>), and [Co&lt;sub>2&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>6&lt;/sub>&lt;i>-&lt;/i>dppa)(&lt;i>μ-&lt;/i>4,4'-bipy)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;i>&lt;sub>n&lt;/sub>&lt;/i>·3&lt;i>n&lt;/i>H&lt;sub>2&lt;/sub>O (&lt;b>3&lt;/b>) were synthesized using a hydrothermal method from Cu(II) and Co(II) metal(II) chlorides, 3-(3,4-dicarboxyphenoxy)phthalic acid (H&lt;sub>4&lt;/sub>dppa), and different auxiliary ligands, namely 2,2'-bipyridine (2,2'-bipy),1,10-phenanthroline (phen), and 4,4'-bipyridine (4,4'-bipy). Products &lt;b>1&lt;/b>-&lt;b>3&lt;/b> were characterized by elemental analysis, FTIR, TGA, PXRD, SEM, and single-crystal X-ray crystallography. The structure of &lt;b>1&lt;/b> features a 1D chain of the 2C1 topological type. Compound &lt;b>2&lt;/b> shows a discrete tetrameric complex. Product &lt;b>3&lt;/b> demonstrates a 3D metal-organic framework (MOF) with the new topology. Their structure and topology, thermal stability, and catalytic activity were studied. In particular, excellent catalytic activity was demonstrated for copper(II)-polymer &lt;b>1&lt;/b> in the cyanosilylation reaction at 35 °C.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>6911</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10574591</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Syntheses, Crystal Structures, and Catalytic Properties of Three Cu(II) and Cobalt(II) Coordination Compounds Based on an Ether-Bridged Tetracarboxylic Acid.</pubmed_title><pmcid>PMC10574591</pmcid><pubmed_authors>Kang X</pubmed_authors><pubmed_authors>Fan X</pubmed_authors><pubmed_authors>Mei Z</pubmed_authors><pubmed_authors>Gu J</pubmed_authors><pubmed_authors>Wang H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Syntheses, Crystal Structures, and Catalytic Properties of Three Cu(II) and Cobalt(II) Coordination Compounds Based on an Ether-Bridged Tetracarboxylic Acid.</name><description>Three new products, [Cu&lt;sub>2&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>3&lt;/sub>&lt;i>-&lt;/i>dppa)(2,2'-bipy)&lt;sub>2&lt;/sub>(H&lt;sub>2&lt;/sub>O)]&lt;i>&lt;sub>n&lt;/sub>&lt;/i>·2&lt;i>n&lt;/i>H&lt;sub>2&lt;/sub>O (&lt;b>1&lt;/b>), [Co&lt;sub>4&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>4&lt;/sub>&lt;i>-&lt;/i>dppa)&lt;sub>2&lt;/sub>(phen)&lt;sub>4&lt;/sub>(H&lt;sub>2&lt;/sub>O)&lt;sub>4&lt;/sub>]·2H&lt;sub>2&lt;/sub>O (&lt;b>2&lt;/b>), and [Co&lt;sub>2&lt;/sub>(&lt;i>μ&lt;/i>&lt;sub>6&lt;/sub>&lt;i>-&lt;/i>dppa)(&lt;i>μ-&lt;/i>4,4'-bipy)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;i>&lt;sub>n&lt;/sub>&lt;/i>·3&lt;i>n&lt;/i>H&lt;sub>2&lt;/sub>O (&lt;b>3&lt;/b>) were synthesized using a hydrothermal method from Cu(II) and Co(II) metal(II) chlorides, 3-(3,4-dicarboxyphenoxy)phthalic acid (H&lt;sub>4&lt;/sub>dppa), and different auxiliary ligands, namely 2,2'-bipyridine (2,2'-bipy),1,10-phenanthroline (phen), and 4,4'-bipyridine (4,4'-bipy). Products &lt;b>1&lt;/b>-&lt;b>3&lt;/b> were characterized by elemental analysis, FTIR, TGA, PXRD, SEM, and single-crystal X-ray crystallography. The structure of &lt;b>1&lt;/b> features a 1D chain of the 2C1 topological type. Compound &lt;b>2&lt;/b> shows a discrete tetrameric complex. Product &lt;b>3&lt;/b> demonstrates a 3D metal-organic framework (MOF) with the new topology. Their structure and topology, thermal stability, and catalytic activity were studied. In particular, excellent catalytic activity was demonstrated for copper(II)-polymer &lt;b>1&lt;/b> in the cyanosilylation reaction at 35 °C.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2025-04-06T02:00:43.663Z</modification><creation>2025-04-06T02:00:43.663Z</creation></dates><accession>S-EPMC10574591</accession><cross_references><pubmed>37836754</pubmed><doi>10.3390/molecules28196911</doi></cross_references></HashMap>