Structural information on trans-1,2-diaminocyclohexane-N,N′-tetraacetateferrate(III) in the solid and aqueous phase

Redox potentials of Ti(IV) and Fe(III) complexes provide insights into titanium biodistribution mechanisms

“…Citrate as an α-hydroxy carboxylic acid is included in our plot, but for reasons described below is not used in the linear least squares analysis. The interactions of these common metal chelators with Fe(III) are well understood and the reduction potentials of many of the corresponding complexes are available in the literature [32][33][34][35][36]. However, few electrochemical data are available for the corresponding Ti(IV) complexes [37][38][39][40].…”

trans-N,N,N′,N′-Tetrakis(carboxymethyl)cyclohexane-1,2-diammonium tetrachloridocadmium(II) tetrahydrate

“…For the structure of 1,2-diaminocyclohexane-N,N 0 -tetraacetate ferrate(III), see: Seibig & Van Eldik (1998). For related tetraacetate-based Cu(II) dimeric and polymeric complexes, see: Wang et al (1999); Ben Amor & Jouini (1999).…”

Tridecaaquadinitratohexasodium(I) bis[(trans-cyclohexane-1,2-diyldinitrilotetraacetato)nickelate(II)]

“…The trans-cyclohexane-1,2-diyldinitrilotetraacetate tetraanion behaves like the edta tetraanion in its chelating behavior; the anion uses its pair of N atoms and its four negatively charged carboxyl O atoms to chelate to first-row transition metal ions in, for example, potassium manganate(II) hydrate (Rettig & Trotter, 1973), tetraaquacopper(II) nickelate(II) trihydrate (Fuertes et al, 1985(Fuertes et al, , 1987, pentasodium aquavanadate(III) (Shimoi et al, 1991), oxonium cobaltate(III) tetrahydrate (Antsyshkina et al, 2000) and pentaaquasodium aquaferrate(III) (Seibig & van Eldik, 1998).…”