Substitution of the internal AsO3– ligand in complex [{Re4As2(AsO)2}(CN)12]8–
- Authors: Pronin A.S.1, Mironov Y.V.1
-
Affiliations:
- Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences
- Issue: Vol 51, No 2 (2025)
- Pages: 114-121
- Section: Articles
- URL: https://rjraap.com/0132-344X/article/view/684590
- DOI: https://doi.org/10.31857/S0132344X25020049
- EDN: https://elibrary.ru/MEGKSW
- ID: 684590
Cite item
Abstract
The reaction of the tetrahedral rhenium arsenide cluster K8[{Re4As2(AsO)2}(CN)12] with molten KF · HF is studied. The reaction affords complex K6[{Re4As2(AsO)F}(CN)12] · 3H2O · KF (I). The substitution of one (µ3-AsO)3– ligand by µ3-F– is shown to occur during the reaction, and the remained internal ligands are not involved in the reaction. The phase purity of the synthesized compound and the absence of impurities of different compositions are confirmed by phase X-ray diffraction (XRD) and mass spectrometry. The structure of complex I is determined by single-crystal XRD (CIF file CCDC no. 2362544).
Keywords
About the authors
A. S. Pronin
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences
Author for correspondence.
Email: pronin@niic.nsc.ru
Russian Federation, Novosibirsk
Yu. V. Mironov
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences
Email: pronin@niic.nsc.ru
Russian Federation, Novosibirsk
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