Bw. Baldwin et al., NEW KEMP DIACID DERIVATIVES GIVE EFFICIENT TRANSPORT AND MODIFIABLE SELECTIVITY FOR ALKALINE-EARTH AND TRANSITION-METAL IONS, Bulletin of the Chemical Society of Japan, 70(8), 1997, pp. 1895-1903
New derivatives of 1,3,5-trimethyl-r-1, c-3, c-5-cyclohexanetricarboxy
lic acid (Kemp's triacid) showed high efficiency for alkaline earth an
d transition metal ion transport through a chloroform liquid membrane.
Simple syntheses from Kemp's triacid or its geometric isomer provided
chelating agents with a tripodal binding site for metal cations. The
tripodal binding site consisted of r-1, c-3-diaxial carboxyl group and
a c-5-amide, ester, or C-methyl group. Alkaline earth metal transport
was quite variable and sensitive to c-5-group changes. For transition
metal transport, c-5-amide diacids gave high total transport efficien
cy. For c-5-ester or C-methyl diacids, complexation of smaller divalen
t cations was decreased, resulting in increased selectivity for large
cations.