(PPh4)[(ReO2S2)CuI] und (NEt4)2[(ReOS3)Cu3Cl4]: Fixierung der bisher nicht isolierten Ionen [ReO2S2]− und [ReOS3]− durch Ausnutzung der Stabilität der CuS2(Re)- und Cu3S3(Re)-Fragmente |
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Authors: | A. Mü ller,A. Hildebrand,E. Krickemeyer,D. S lter,H. B gge,A. Armatage |
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Affiliation: | A. Müller,A. Hildebrand,E. Krickemeyer,D. Sölter,H. Bögge,A. Armatage |
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Abstract: | (PPh4)[(ReO2S2)CuI] and (NEt4)2[ReOS3)Cu3Cl4]: Fixation of the up to now not Isolated Ions [ReO2S2]? and [ReOS3]? Utilizing the Stability of the CuS2(Re) and Cu3S3(Re) Fragments (PPh4)[(ReO2S2)CuI] ( 1 ) and (NEt4)2[ReOS3)Cu3Cl4] ( 2 ) containing the up to now not isolated oxothioperrhenate ions [ReO2S2]? and [ReOS3]? as ligands, have been prepared by the reaction of (NEt4)[ReS4] with PPh3 and CuI in acetone in the presence of (PPh4)I (( 1 )) or with CuCl in CH2Cl2 in the presence of (NEt4)Cl (( 2 )), respectively. 1 and 2 have been characterized by X-ray structure analysis, elemental analysis and spectroscopic studies (IR, UV/Vis). The electronic spectra show bands which can approximately be assigned to interesting low-energy charge-transfer-transitions of the type d(Cu) → d(Re). For crystal data see Inhaltsübersicht. |
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Keywords: | Oxothioperrhenate ions, ReO2S2− , ReOS3− preparation crystal structure IR, UV/Vis spectra |
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