Substitution of the internal AsO3– ligand in complex [{Re4As2(AsO)2}(CN)12]8–

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Resumo

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).

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Sobre autores

A. Pronin

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences

Autor responsável pela correspondência
Email: pronin@niic.nsc.ru
Rússia, Novosibirsk

Yu. Mironov

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences

Email: pronin@niic.nsc.ru
Rússia, Novosibirsk

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2. Fig. 1. Structure of the anion [{Re4As2(AsO)F}(CN)12]6–. Atoms of the symmetrically independent part are numbered. Thermal ellipsoids of 50% probability are shown.

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3. Fig. 2. Scheme of the reaction of substitution of one internal ligand (AsO)3– by F– in the anion [{Re4As2(AsO)F}(CN)12]6–.

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4. Fig. 3. Scheme of the reaction of substitution of one internal ligand (AsO)3– by F– in the anion [{Re4As2(AsO)F}(CN)12]6–.

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5. Fig. 4. IR spectra of compound I (black line) and the starting complex K8[{Re4As2(AsO)2}(CN)12] 12H2O (red line).

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6. Fig. 5. Fragment of the mass spectrum of an aqueous solution of complex I.

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