Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1309024 | Inorganica Chimica Acta | 2008 | 5 Pages |
Two dinuclear metal complexes, [Co2(bhmp)(MeCO2)2]ClO4 · 2H2O (1) and [Ni2(bhmp)(MeCO2)2]ClO4 · 2H2O (2), were synthesized with a dinucleating ligand, 2,6-bis[bis(2-hydroxyethyl)aminomethyl]-4-methylphenol [H(bhmp)]. Both complexes were easily soluble in water as well as in DMF. Electronic spectra for both complexes were measured in both solvents and analyzed using the angular overlap model (AOM). From the electronic spectra and molar conductance, both complexes were determined to exist as [M2(bhmp)(MeCO2)2]+ (M = CoII or NiII) in DMF, dissociating perchlorate ions. On the other hand, in water, it was concluded that the acetate ions were partially dissociated and each complex existed as a mixture of some dissociated species, such as [M2(bhmp)(MeCO2)(H2O)2]2+ and [M2(bhmp)(H2O)4]3+ (M = CoII or NiII). Such dissociation was also confirmed by precipitation of the dissociated species when NaBPh4 was added into an aqueous solution of the nickel complex.
Graphical abstractDinuclear metal complexes, [Co2(bhmp)(MeCO2)2]ClO4 · 2H2O (1) and [Ni2(bhmp)(MeCO2)2]ClO4 · 2H2O (2), were synthesized with a dinucleating ligand, 2,6-bis[bis(2-hydroxyethyl)aminomethyl]-4-methylphenol [H(bhmp)], and both complexes were easily soluble in water as well as in DMF.Figure optionsDownload full-size imageDownload as PowerPoint slide