Ornela B.T. Tchougong , Carole F.N. Nguemdzi , Bridget N. Ndosiri , Ledoux S. Pouamo , Colince Nde , Mohammad Azam , Frédéric Capet , Michel Foulon , Justin Nenwa
{"title":"A polymeric Co(II) oxalate salt containing pyridinium type cations: Synthesis, structure, spectroscopy, thermal behavior and magnetism","authors":"Ornela B.T. Tchougong , Carole F.N. Nguemdzi , Bridget N. Ndosiri , Ledoux S. Pouamo , Colince Nde , Mohammad Azam , Frédéric Capet , Michel Foulon , Justin Nenwa","doi":"10.1016/j.poly.2024.117238","DOIUrl":null,"url":null,"abstract":"<div><div>A Co(II) oxalate coordination polymer, (C<sub>7</sub>H<sub>11</sub>N<sub>2</sub>)<sub>2</sub>[Co(C<sub>2</sub>O<sub>4</sub>)<sub>2</sub>]·5H<sub>2</sub>O (<strong>1</strong>) (C<sub>7</sub>H<sub>11</sub>N<sub>2</sub><sup>+</sup> = 2-amino-4,6-dimethylpyridinium cation), has been synthesized and characterized by elemental and thermal analyses, FT-IR and UV/Vis spectroscopies, powder X-ray diffraction (PXRD), single-crystal X-ray diffraction and variable temperature magnetic susceptibility measurements. Compound <strong>1</strong> is a polymerized organic–inorganic hybrid salt, the asymmetric unit of which consists of one Co(II) ion, one bidentate C<sub>2</sub>O<sub>4</sub><sup>2−</sup> ligand, two halves of bidentate C<sub>2</sub>O<sub>4</sub><sup>2−</sup> ligands, two 2-amino-4,6-dimethylpyridinium C<sub>7</sub>H<sub>11</sub>N<sub>2</sub><sup>+</sup> cations and five crystal water molecules. Each Co<sup>II</sup> center is six-coordinated in a distorted octahedral geometry fulfilled by six oxygen atoms from three chelating C<sub>2</sub>O<sub>4</sub><sup>2−</sup> ligands. The [Co(C<sub>2</sub>O<sub>4</sub>)<sub>2</sub>]<sup>2−</sup> ions act as complex ligands and efficiently bridge neighboring Co<sup>2+</sup> ions, forming chains of complex anions linked by hydrogen bonded water molecules. Hydrogen bonding interactions of the type O<img>H∙∙∙O and N<img>H∙∙∙O along with π–π stacking interactions between pyridine rings contribute to the stabilization of the 3D supramolecular framework. Temperature-dependence magnetic moment (<em>µ</em>) collected under zero-field cooled (ZFC) and field-cooled (FC) conditions revealed weak antiferromagnetic ordering at low temperatures.</div></div>","PeriodicalId":20278,"journal":{"name":"Polyhedron","volume":"264 ","pages":"Article 117238"},"PeriodicalIF":2.4000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polyhedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0277538724004145","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
A Co(II) oxalate coordination polymer, (C7H11N2)2[Co(C2O4)2]·5H2O (1) (C7H11N2+ = 2-amino-4,6-dimethylpyridinium cation), has been synthesized and characterized by elemental and thermal analyses, FT-IR and UV/Vis spectroscopies, powder X-ray diffraction (PXRD), single-crystal X-ray diffraction and variable temperature magnetic susceptibility measurements. Compound 1 is a polymerized organic–inorganic hybrid salt, the asymmetric unit of which consists of one Co(II) ion, one bidentate C2O42− ligand, two halves of bidentate C2O42− ligands, two 2-amino-4,6-dimethylpyridinium C7H11N2+ cations and five crystal water molecules. Each CoII center is six-coordinated in a distorted octahedral geometry fulfilled by six oxygen atoms from three chelating C2O42− ligands. The [Co(C2O4)2]2− ions act as complex ligands and efficiently bridge neighboring Co2+ ions, forming chains of complex anions linked by hydrogen bonded water molecules. Hydrogen bonding interactions of the type OH∙∙∙O and NH∙∙∙O along with π–π stacking interactions between pyridine rings contribute to the stabilization of the 3D supramolecular framework. Temperature-dependence magnetic moment (µ) collected under zero-field cooled (ZFC) and field-cooled (FC) conditions revealed weak antiferromagnetic ordering at low temperatures.
期刊介绍:
Polyhedron publishes original, fundamental, experimental and theoretical work of the highest quality in all the major areas of inorganic chemistry. This includes synthetic chemistry, coordination chemistry, organometallic chemistry, bioinorganic chemistry, and solid-state and materials chemistry.
Papers should be significant pieces of work, and all new compounds must be appropriately characterized. The inclusion of single-crystal X-ray structural data is strongly encouraged, but papers reporting only the X-ray structure determination of a single compound will usually not be considered. Papers on solid-state or materials chemistry will be expected to have a significant molecular chemistry component (such as the synthesis and characterization of the molecular precursors and/or a systematic study of the use of different precursors or reaction conditions) or demonstrate a cutting-edge application (for example inorganic materials for energy applications). Papers dealing only with stability constants are not considered.