<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(6)</volume><submitter>Pantelis KN</submitter><pubmed_abstract>A relatively unexplored synthetic route in redox-active Mn(II/III) coordination chemistry has been employed toward the preparation of a new mixed-valence MnII/III 1-D linear chain from the reaction of [MnIII(sacb)2]- precursor with a MnII source, where sacbH2 is the Schiff base ligand N-salicylidene-2-amino-5-chlorobenzoic acid. The mononuclear (Pr2NH2)[MnIII(sacb)2] (1) compound was obtained in excellent yields (>85%) from the 1:2:3 reaction of Mn(O2CMe)2∙4H2O, sacbH2 and Pr2NH, respectively. In 1, the two doubly deprotonated sacb2- ligands act as Ocarboxylate,Nimine,Ophenoxide-tridentate chelates, while the second carboxylate O atom of sacb2- is dangling and H-bonded to the Pr2NH2+ countercation. Complex 1 was subsequently used as a 'ligand' to react stoichiometrically with the 'metal' Mn(NO3)2∙4H2O, thus leading to the 1-D coordination polymer {[MnIIMnIII(sacb)2(H2O)2(MeOH)2](NO3)}n (2) in good yields (~50%). The removal of Pr2NH2+ from the vicinity of the [MnIII(sacb)2]- metalloligand has rendered possible (vide infra) the coordination of the second Ocarboxylate of sacb2- to neighboring {MnII(H2O)2(MeOH)2}2+ units, and consequently the formation of the 1-D polymer 2. Direct-current (dc) magnetic susceptibility studies revealed the presence of very weak antiferromagnetic exchange interactions between alternating MnIII and MnII atoms with a coupling constant of J = -0.08 cm-1 for g = 2.00. The combined results demonstrate the potential of the 'metal complexes as ligands' approach to yield new mixed-valence Mn(II/III) coordination polymers with interesting structural motifs and physicochemical properties.</pubmed_abstract><journal>Materials (Basel, Switzerland)</journal><pagination>E1352</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7143807</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>'Metal Complexes as Ligands' for the Synthesis of Coordination Polymers: A MnIII Monomer as a Building Block for the Preparation of an Unprecedented 1-D {MnIIMnIII}n Linear Chain.</pubmed_title><pmcid>PMC7143807</pmcid><pubmed_authors>Lampropoulos C</pubmed_authors><pubmed_authors>Cunha-Silva L</pubmed_authors><pubmed_authors>Pantelis KN</pubmed_authors><pubmed_authors>Escuer A</pubmed_authors><pubmed_authors>Stamatatos TC</pubmed_authors><pubmed_authors>Karotsis G</pubmed_authors></additional><is_claimable>false</is_claimable><name>'Metal Complexes as Ligands' for the Synthesis of Coordination Polymers: A MnIII Monomer as a Building Block for the Preparation of an Unprecedented 1-D {MnIIMnIII}n Linear Chain.</name><description>A relatively unexplored synthetic route in redox-active Mn(II/III) coordination chemistry has been employed toward the preparation of a new mixed-valence MnII/III 1-D linear chain from the reaction of [MnIII(sacb)2]- precursor with a MnII source, where sacbH2 is the Schiff base ligand N-salicylidene-2-amino-5-chlorobenzoic acid. The mononuclear (Pr2NH2)[MnIII(sacb)2] (1) compound was obtained in excellent yields (>85%) from the 1:2:3 reaction of Mn(O2CMe)2∙4H2O, sacbH2 and Pr2NH, respectively. In 1, the two doubly deprotonated sacb2- ligands act as Ocarboxylate,Nimine,Ophenoxide-tridentate chelates, while the second carboxylate O atom of sacb2- is dangling and H-bonded to the Pr2NH2+ countercation. Complex 1 was subsequently used as a 'ligand' to react stoichiometrically with the 'metal' Mn(NO3)2∙4H2O, thus leading to the 1-D coordination polymer {[MnIIMnIII(sacb)2(H2O)2(MeOH)2](NO3)}n (2) in good yields (~50%). The removal of Pr2NH2+ from the vicinity of the [MnIII(sacb)2]- metalloligand has rendered possible (vide infra) the coordination of the second Ocarboxylate of sacb2- to neighboring {MnII(H2O)2(MeOH)2}2+ units, and consequently the formation of the 1-D polymer 2. Direct-current (dc) magnetic susceptibility studies revealed the presence of very weak antiferromagnetic exchange interactions between alternating MnIII and MnII atoms with a coupling constant of J = -0.08 cm-1 for g = 2.00. The combined results demonstrate the potential of the 'metal complexes as ligands' approach to yield new mixed-valence Mn(II/III) coordination polymers with interesting structural motifs and physicochemical properties.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Mar</publication><modification>2025-05-29T20:05:09.589Z</modification><creation>2025-05-29T20:05:09.589Z</creation></dates><accession>S-EPMC7143807</accession><cross_references><pubmed>32192062</pubmed><doi>10.3390/ma13061352</doi></cross_references></HashMap>