Three double-armed diazacrown ethers with two thiophene side groups, h
enyl-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane (DTDC), enoyl-1,4,10
,13-tetraoxa-7,16-diazacyclooctadecane (DTODC), and etyl)-1,4,10,13-te
traoxa-7,16-diazacyclooctadecane (DTAODC), have been synthesized and u
sed as novel neutral lead(II) ionophores in ion selective electrode ap
plications. The relationship between the molecular structure of these
ionophores and electrochemical properties (linear range, response time
, selectivity) of the membrane electrode is discussed. The optimum con
ditions for the preparation of the electrodes are described. The optim
ized dithenoyldiazacrown had a detection limit of pPb = 5.7, and Nerns
tian range with slope 29.2 mV decade(-1) from pPb = 5.0 to 2.7. Mercur
y and silver ions are the major interferences. These electrodes are ap
plied to potentiometric titrations of lead(II) ions and show promise f
or the determination of lead ions in water samples.