Synthesis of tetra-N-substituted 1,10-dioxa-4,7,13,16-tetraazacyclooctadecanes and their application as lead (II) selective electrodes. X-ray crystalstructure of 4,7,13,16-tetrathenoyl-1,10-dioxa-4,7, 13,16-tetraazacyclooctadecane

Citation
Xh. Yang et al., Synthesis of tetra-N-substituted 1,10-dioxa-4,7,13,16-tetraazacyclooctadecanes and their application as lead (II) selective electrodes. X-ray crystalstructure of 4,7,13,16-tetrathenoyl-1,10-dioxa-4,7, 13,16-tetraazacyclooctadecane, J INCL P MA, 33(2), 1999, pp. 135-148
Citations number
20
Categorie Soggetti
Chemistry
Journal title
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY
ISSN journal
13883127 → ACNP
Volume
33
Issue
2
Year of publication
1999
Pages
135 - 148
Database
ISI
SICI code
1388-3127(199902)33:2<135:SOT1>2.0.ZU;2-X
Abstract
Terra-N-substituted 1,10-dioxa-4,7,13,16-tetraazacyclooctadecanes (tetraaza crown ethers) (1-5) have been synthesised. Each compound was incorporated i n a PVC membrane that provided the basis for a lead-selective potentiometri c electrode. The electrode based on the 4,7,13,16-tetrathenoyl-1,l 10-dioxa -4,7,13,1 6-tetraazacyclooctadecane (5) ionophore bearing four thenoyl func tional subunits exhibited excellent lead (II) ion selectivity with only Ag and Hg2+ significantly interfering. The crystal structure of this host (5) has been determined by single crysral X-ray analysis. Crystal data. C32H36 N4O6S4, M 700.9, monoclinic, space group P2(1)/c, a, 10,315(4), b, 13.635(2 ), c, 14.357(6)Angstrom, beta 124.63(2)degrees, V 1661.6(9)Angstrom(3), D-c , 1.40 g cm(-3), Z 2, mu(Cu), 29.90 cm-l. Final residuals R, R, were 0.054, 0.082 for the observed data.