Adducts of zinc and copper(II) dialkyldithiocarbamate complexes with dialkylamines: Synthesis, EPR, and 13C and 15N CP/MAS NMR
| Autor: | A. S. Zaeva, Alexander V. Ivanov, T. A. Rodina, E. V. Novikova, Willis Forsling |
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| Rok vydání: | 2007 |
| Předmět: |
chemistry.chemical_classification
Materials Science (miscellaneous) Inorganic chemistry chemistry.chemical_element Zinc Mesomeric effect Copper law.invention Inorganic Chemistry Trigonal bipyramidal molecular geometry Crystallography chemistry.chemical_compound chemistry law Physical and Theoretical Chemistry Dithiocarbamate Electron paramagnetic resonance Inductive effect Alkyl |
| Zdroj: | Russian Journal of Inorganic Chemistry. 52:691-697 |
| ISSN: | 1531-8613 0036-0236 |
| Popis: | Crystalline adducts of zinc and copper(II) dithiocarbamate (Dtc) complexes with dialkylamines [M(NHR′2)(S2CNR2)2] (M = Zn, 63Cu, 65Cu; R = CH3, C2H5, or R2 = (CH2)4O; R′ = C2H5, C3H7) have been preparatively isolated. The structures and spectral properties of the adducts have been studied by EPR and 13C and 15N MAS NMR. Chemisorption of bases on powders of dinuclear dithiocarbamates leads to their dissociation into monomeric adducts. Computer simulation demonstrates that the experimental EPR spectra of isotope-substituted copper(II) adducts have an individual character. The geometry of the copper polyhedra is intermediate between a trigonal bipyramid (TBP) and a tetragonal pyramid (TP). The TBP and TP contributions have been quantified based on EPR data. 13C and 15N MAS NMR data show that the Dtc ligands incorporated into the zinc adduct molecule are structurally nonequivalent. The dependence of the isotropic 15N chemical shifts of the Dtc groups on the alkyl substituents at the nitrogen atom is interpreted based on the concept of joint manifestation of the (+)inductive effect of the alkyl substituents and the mesomeric effect of the Dtc groups. |
| Databáze: | OpenAIRE |
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