cis- and trans-Isomerism in Manganese(II) Complexes with Acylpyrazolonepyridine
The reaction between 1-(5-hydroxy-1-methyl-3-(pyridin-2-yl)-1H-pyrazol-4-yl)ethan-1-one (L) and manganese(II) acetate afforded two new manganese(II) complexes with trans and cis configurations of the acylpyrazolone ligands—trans-L2Mn(MeOH)2 (trans-I) and cis-L2Mn(MeOH)2 (cis-I),—characterized by elemental analysis and X-ray diffraction (CCDC nos. 2408806 and 2408805, respectively). The less stable (cis-I) complex was obtained by introducing 2,2′-bipyridine into the reaction, presumably leading to the formation of an intermediate heteroleptic complex with L and 2,2′-bipyridine. The resulting isomeric complexes exhibit different molecular geometries and supramolecular organization in the crystal but convert into the more stable (trans-I) isomer in DMF solution. According to magnetometry and EPR spectroscopy, they display slightly different magnetic properties.
Authors
- A.S. Bogomyakov (ORCID: https://orcid.org/0000-0002-6918-5459)
- A. V. Borodulina (ORCID: https://orcid.org/0009-0001-1876-8267)
- И. А. Никовский
- Yulia Vladimirovna Nelyubina (ORCID: https://orcid.org/0000-0002-9121-0040)
- A. N. Sinel’nikov
Institutions
- Moscow Institute of Physics and Technology (RU)
- Novosibirsk State University (RU)
- A. N. Nesmeyanov Institute of Organoelement Compounds (RU)
- International Tomography Center (RU)
Publication Details
- Journal
- Russian Journal of Coordination Chemistry
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1134/s1070328424601547
- Primary Topic
- Magnetism in coordination complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.00