ARTIFICIAL ALLOSTERIC IONOPHORES - REGULATION OF ION RECOGNITION OF POLYETHERS BEARING BIPYRIDINE MOIETIES BY COPPER(I)

Citation
T. Nabeshima et al., ARTIFICIAL ALLOSTERIC IONOPHORES - REGULATION OF ION RECOGNITION OF POLYETHERS BEARING BIPYRIDINE MOIETIES BY COPPER(I), Inorganic chemistry, 32(8), 1993, pp. 1407-1416
Citations number
51
Journal title
ISSN journal
00201669
Volume
32
Issue
8
Year of publication
1993
Pages
1407 - 1416
Database
ISI
SICI code
0020-1669(1993)32:8<1407:AAI-RO>2.0.ZU;2-L
Abstract
Artificial allosteric ionophores, oligoethylene glycols bearing 2,2-bi pyridine derivatives at the termini, were synthesized. Solvent extract ion experiment indicated that the polyethers bind Cu+ firmly and selec tively among heavy metal ions because of a chelate and a steric effect of the two bipyridines on the ligation. The complexation with Cu+ tak es place rapidly and quantitatively in organic media to result in intr amolecular cyclization of the linear polyether moiety, giving a novel type of crown ethers, pseudocrown ethers. The UV-vis and H-1 NMR spect roscopies indicated that the bipyridine complexes have a tetrahedral g eometry. Allosteric regulation of ion recognition (heterotropic cooper ativity) has been performed successfully in transport experiment throu gh a liquid membrane (methylene chloride) by using the ionophore and C u+ as an effector. The transport selectivity to alkali metal ions was dramatically enhanced by the addition of Cu+ due to the formation of t he cyclic framework. The transport experiment and measurement of uptak e and release rates of ionophores for alkali metals suggested that the remarkably high transport selectivity results from a suitable cavity size of the pseudocrown ring and electrostatic repulsion between alkal i metal and Cu+ ions bound in the same ionophore. Moreover the pseudoc rowns exhibit molecular chirality at -28-degrees-C in the presence of excess Pirkle's reagent, but racemization occurs at room temperature. In contrast, a pseudocrown formed from Cu+ and a polyether with four b ipyridines maintains its molecular chirality even at room temperature, promising application of the pseudocrowns to asymmetric recognition. The facts obtained here indicate clearly that our strategy, conversion of a linear polyether with heavy metal binding sites to the correspon ding pseudocrown by the addition of heavy metals, is quite convenient and powerful for modulation of molecular recognition and molecular inf ormation.