<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(23)</volume><submitter>Veselovsky VV</submitter><pubmed_abstract>The new homochiral 1D metal-organic coordination polymer [Cu2(EDPB)•H2O]n was synthesized starting from the original 3,3'-ethyne-1,2-diylbis[6-(L-prolylamino)benzoic acid] (H4EDPB). The unique crystal structure of the new compound was established by powder X-ray diffraction. The [Cu2(EDPB)•H2O]n system shows catalytic activity and enantioselectivity in a Henry reaction of p-nitrobenzaldehyde with nitromethane.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>8376</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9738848</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and the Crystal Structure of a New Chiral 1D Metal-Organic Coordination Polymer Based on L-Prolineamide-Substituted Diarylacetylenedicarboxylic Acid Derivative.</pubmed_title><pmcid>PMC9738848</pmcid><pubmed_authors>Isaeva VI</pubmed_authors><pubmed_authors>Veselovsky VV</pubmed_authors><pubmed_authors>Kustov LM</pubmed_authors><pubmed_authors>Chernyshev VV</pubmed_authors><pubmed_authors>Nissenbaum VD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and the Crystal Structure of a New Chiral 1D Metal-Organic Coordination Polymer Based on L-Prolineamide-Substituted Diarylacetylenedicarboxylic Acid Derivative.</name><description>The new homochiral 1D metal-organic coordination polymer [Cu2(EDPB)•H2O]n was synthesized starting from the original 3,3'-ethyne-1,2-diylbis[6-(L-prolylamino)benzoic acid] (H4EDPB). The unique crystal structure of the new compound was established by powder X-ray diffraction. The [Cu2(EDPB)•H2O]n system shows catalytic activity and enantioselectivity in a Henry reaction of p-nitrobenzaldehyde with nitromethane.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-20T03:34:11.057Z</modification><creation>2025-04-20T03:34:11.057Z</creation></dates><accession>S-EPMC9738848</accession><cross_references><pubmed>36500469</pubmed><doi>10.3390/molecules27238376</doi></cross_references></HashMap>