Structural investigation of nickel(II) complexes with bidentate aminoether ligands in solution based on the electronic spectra
| Autor: | Hiroshi Sakiyama, Yoshio Watanabe, Takashi Tokue, Katsuya Tone, Ryo Yamaguchi, Eiji Asato, Yusuke Tamashiro |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
Ligand field theory
Denticity Chemistry chemistry.chemical_element Spectral line Inorganic Chemistry chemistry.chemical_compound Crystallography Nickel Monomer Computational chemistry Octahedral molecular geometry Materials Chemistry Dimethylformamide Density functional theory Physical and Theoretical Chemistry |
| Zdroj: | Polyhedron. 96:44-50 |
| ISSN: | 0277-5387 |
| DOI: | 10.1016/j.poly.2015.04.025 |
| Popis: | For the purpose of investigating molecular structures in solution based on electronic spectra, two mononuclear nickel(II) complexes, [Ni(moen) 2 (DMF) 2 ](BPh 4 ) 2 ( 1 ) and [Ni(thfn) 2 (DMF) 2 ](BPh 4 ) 2 ( 2 ), were newly prepared using bidentate aminoether ligands [moen = 2-methoxyethylamine; thfn = 2-tetrahydrofurfurylamine; DMF = N , N -dimethylformamide]. Judging from the molar conductance, the complexes are considered to exist as monomeric cations in DMF solution. The electronic spectra of the complexes were measured in DMF and the spectra were typical for an octahedral geometry for both complexes, showing three spin-allowed d–d transition bands. Using the Gaussian curve fitting method, the spin-allowed bands were found to show a 2:1, 1:2 and 1:2 splitting pattern from lower to higher energy, which corresponds to a tetragonally elongated geometry. That is, the axial ligand field is weaker than the equatorial ligand field, and the ether oxygen atoms are considered to be in trans -positions. In order to ascertain the structures in solution, conformational analysis was conducted based on density functional theory (DFT) computations. The DFT results provided detailed structures which are consistent with the spectroscopic results. |
| Databáze: | OpenAIRE |
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