Issue 10, 1995

Lipophilic hexadentate gallium, indium and iron complexes of new phenolate-derivatized cyclohexanetriamines as potential in vivo metal-transfer reagents

Abstract

1,3,5-Tris(5-substituted salicylamino)cyclohexanes (H3L; R = H, NO2 or OMe) have been synthesized by Schiff-base condensation between cis-1,3,5-triaminocyclohexane and a substituted salicylaldehyde, followed by reduction with KBH4. Reaction of these compounds with gallium(III), indium(III) and iron(III) salts gave neutral six-co-ordinate N3O3 complexes of type [ML](M = Ga, In or Fe). The complexes have been characterized by a combination of infrared, 1H and 13C-{1H} NMR and mass spectroscopy. The distribution coefficients between octan-1-ol and water indicate that the complexes are lipophilic. The electronic absorption spectra of the high-spin iron(III) complexes show ligand-to-metal charge-transfer bands in the 450–500 nm range. The structures of five of the complexes have been confirmed by single-crystal X-ray crystallography.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1995, 1677-1688

Lipophilic hexadentate gallium, indium and iron complexes of new phenolate-derivatized cyclohexanetriamines as potential in vivo metal-transfer reagents

J. E. Bollinger, J. T. Mague, C. J. O′Connor, W. A. Banks and D. M. Roundhill, J. Chem. Soc., Dalton Trans., 1995, 1677 DOI: 10.1039/DT9950001677

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