Solvated copper(I) hexafluorosilicate π-complexes based on [Cu2(amtd)2]2+ (amtd = 2-allylamino-5-methyl-1,3,4-thiadiazole) dimer
Autor: | Evgeny Goreshnik, Dmitry Morozov, B. R. Ardan, Gleb Veryasov, M. G. Mys'kiv, Yu. I. Slyvka |
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Rok vydání: | 2016 |
Předmět: |
computational modeling
Dimer Inorganic chemistry copper(I) hexafluorosilicates chemistry.chemical_element 010402 general chemistry 010403 inorganic & nuclear chemistry Electrochemistry 01 natural sciences Biochemistry Inorganic Chemistry chemistry.chemical_compound Hydrolysis symbols.namesake raman spectroscopy Materials Chemistry Mother liquor Physical and Theoretical Chemistry Acetonitrile ta116 heterocycles Organic Chemistry Copper 0104 chemical sciences chemistry symbols Physical chemistry Raman spectroscopy |
Zdroj: | Journal of Organometallic Chemistry. 810:1-11 |
ISSN: | 0022-328X |
DOI: | 10.1016/j.jorganchem.2016.03.001 |
Popis: | [Cu2(amdt)2]SiF6·C6H6 and [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O (amdt = 2-allylamino-5- methyl-1,3,4-thiadiazole) were obtained by alternating-current electrochemical synthesis, starting from water–acetonitrile–benzene mixtures containing 2-allylamino-5-methyl-1,3,4- thiadiazole and CuSiF6·4H2O. The electrochemical reduction of the saturated copper hexafluorosilicate water solution beneath the neatly poured layer of acetonitrile-benzene amdt solution resulted in the formation of crystalline [Cu2(amdt)2]SiF6·C6H6. The initial stirring of the same mixture before subjecting it to the electrochemical reduction resulted in the formation of [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O. A sluggish hydrolysis of the acetonitrile over 2 years in a closed test tube with [Cu2(amdt)2]SiF6·C6H6 crystals in a mother liquor resulted in the formation of [Cu2L2(H2O)2]SiF6·CH3CONH2·2H2O. All the compounds were studied using X-ray single-crystal diffraction and Raman spectroscopy. The molecular structures and the Raman spectra of the compounds were discussed on the basis of computational modeling with the DFT/B3LYP/cc-pVDZ method. peerReviewed |
Databáze: | OpenAIRE |
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