NEW KEMP DIACID DERIVATIVES GIVE EFFICIENT TRANSPORT AND MODIFIABLE SELECTIVITY FOR ALKALINE-EARTH AND TRANSITION-METAL IONS

Citation
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
Citations number
25
Categorie Soggetti
Chemistry
ISSN journal
00092673
Volume
70
Issue
8
Year of publication
1997
Pages
1895 - 1903
Database
ISI
SICI code
0009-2673(1997)70:8<1895:NKDDGE>2.0.ZU;2-1
Abstract
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.