SYNTHETIC IONOPHORES - PART 17 - SYNTHESIS OF ETHER-AMINE-AMIDE BASEDM-CYCLOPHANES - A SEARCH FOR PB2+ SELECTIVE IONOPHORES

Citation
S. Kumar et al., SYNTHETIC IONOPHORES - PART 17 - SYNTHESIS OF ETHER-AMINE-AMIDE BASEDM-CYCLOPHANES - A SEARCH FOR PB2+ SELECTIVE IONOPHORES, Journal of inclusion phenomena and molecular recognition in chemistry, 32(1), 1998, pp. 47-56
Citations number
18
Categorie Soggetti
Chemistry,Crystallography
Journal title
Journal of inclusion phenomena and molecular recognition in chemistry
ISSN journal
09230750 → ACNP
Volume
32
Issue
1
Year of publication
1998
Pages
47 - 56
Database
ISI
SICI code
0923-0750(19980121)32:1<47:SI-P1->2.0.ZU;2-1
Abstract
m-Cyclophanes 3, 4, and 5 possessing two ether oxygen, two amide, one NH and a pi-system, an optimal combination of ligating sites for selec tive Pb2+ binding, have been synthesized by condensations of diethylen etriamine, 3,3'-diaminodipropylamine and 1,3-diaminopropane with 1,3-b is(ethoxycarbonylmethoxy) benzene (6) formed by the PTC reaction of re sorcinol and ethyl chloroacetate. Ionophores 3-5 induced cation extrac tion/transport could not be studied due to their insolubility in CHCl3 /CH2Cl2 and solubility in water, but (CNMR)-C-13 titrations of 4 with metal ions point to its binding preferences for Ag+ and Pb2+ over alka li/alkaline earth cations.