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
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.