6533b7d8fe1ef96bd126aeca
RESEARCH PRODUCT
Solvated copper(I) hexafluorosilicate π-complexes based on [Cu2(amtd)2]2+ (amtd = 2-allylamino-5-methyl-1,3,4-thiadiazole) dimer
Evgeny GoreshnikDmitry MorozovB. R. ArdanGleb VeryasovM. G. Mys'kivYu. I. Slyvkasubject
computational modelingDimerInorganic chemistrycopper(I) hexafluorosilicateschemistry.chemical_element010402 general chemistry010403 inorganic & nuclear chemistryElectrochemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundHydrolysissymbols.namesakeraman spectroscopyMaterials ChemistryMother liquorPhysical and Theoretical ChemistryAcetonitrileta116heterocyclesOrganic ChemistryCopper0104 chemical scienceschemistrysymbolsPhysical chemistryRaman spectroscopydescription
[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
year | journal | country | edition | language |
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2016-05-01 | Journal of Organometallic Chemistry |