Amb motiu del tancament d'estiu, la validació de documents es reprendrà a partir del 28 d'agost de 2026. Disculpeu les molèsties.
Con motivo del cierre de verano, la validación de documentos se reanudará a partir del 28 de agosto de 2026. Disculpad las molestias
Due to the summer closure, document validation will resume starting August 28, 2026. We apologize for any inconvenience.

Document type

Article

Version

Published version

Publication date

Publication license

cc-by (c) Pantelis, Konstantinos N et al., 2020
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/173732

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

Journal Title

Director/Tutor

Journal ISSN

Volume Title

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.

Citation

Citation

PANTELIS, Konstantinos N., et al. 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. Materials. 2020. Vol. 13(6), num. 1352. ISSN 1996-1944. [consulted: 16 of August of 2026]. Available at: https://hdl.handle.net/2445/173732

Export metadata

JSON - METS

Share record