The reactions of manganese(II), cobalt(II) and nickel(II) acetates (1 mole) with antipyrine-4-azo-fl-ethylcyanoacetate (HL 1) and antipyrine-4-azo-fl-acetylacetone (HL 2) (1 mole) produce complexes of the M(L)2 type. K2PdC14 (lmole) reacts with HL a and HL 2 (lmole) to yield complexes of the general
✦ LIBER ✦
Chelate complexes of manganese(II): Synthesis, spectroscopic and electron paramagnetic resonance properties of manganese(II) β-diketonate derivatives
✍ Scribed by Giorgio Mercati; Franca Morazzoni; Luciana Naldini; Sandra Seneci
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 760 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0020-1693
No coin nor oath required. For personal study only.
✦ Synopsis
The results of e.s.r., vibrational and electronic investigations were compared in order to describe the ligand field properties, the charge distribution and the nature of the chemical bonds in the adducts of bis-(2,4-pentanedionato)manganese(II) (Mn(pd)z) with basic molecules. E.s.r. data are suitable to describe axial and rhombic distortions caused by the additional base molecules. Phenanthroline, pyrazine and ethylenediamine give rise to axial distortion; dipyridyl, pyridine, I-Mepyridine, quinoline, quinoxaline, water ' to rhombic distortion. Both the sterk hindrance and the electronic properties of the additional base ligand contribute to the distortion; however the electron-withdrawing power of the base decides the distortion weight. Intermolecular interaction in Mn(pd)z and in the adduct with pyrazine have also been considered by the e.s.r. data. The manganese-pentanedionato bond properties and the bond strength internal to pentanedionato have been discussed by the i.r. data, in the light of the metal electronic structure and of the II acceptor properties of the additional base; the competition between pentanedionato and the additional base, as
for the R acceptor power, is favourable to the pentanedionato ligand.
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