Abstract
The ionic complexes [Ph3PR][Au(CN)2Cl2] (R = CH2CH=CHCH3 (I), CH2CN (II)) were prepared by the reactions of organyltriphenylphosphonium chlorides with potassium dichlorodicyanoaurate in water followed by recrystallization from acetonitrile. Apart from the major product II, the crystals of the molecular complex Ph3PC(H)(CN)Au(CN)2Cl (III) were isolated. The products were characterized by X-ray diffraction (CIF files CCDC nos. 1957185 (I), 2060227 (II), 2066549 (III)) and NMR and IR spectroscopy. According to X-ray diffraction data, complexes I and II consisted of organyltriphenylphosphonium cations with a slightly distorted tetrahedral geometry of phosphorus atoms and the centrosymmetric square anions [Au(CN)2Cl2]−, which, in the case of complex II, form coordination pseudopolymer chains via the Au∙∙∙Cl interanion contacts (3.40 Å). In complex III, the phosphorus and gold atoms are also coordinated in the tetrahedral and square environments; the ylide carbon atom is located at the gold atom in the trans-position relative to chlorine.
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Shevchenko, D.P., Khabina, A.E., Sharutin, V.V. et al. Synthesis and Structure of Gold Complexes [Ph3PR][Au(CN)2Cl2] (R = CH2CH=CHCH3, CH2CN) and Ph3PC(H)(CN)Au(CN)2Cl. Russ J Coord Chem 48, 26–32 (2022). https://doi.org/10.1134/S1070328422010055
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DOI: https://doi.org/10.1134/S1070328422010055