Novel fluoroionophores bearing two (1) and one (2) fluorophoric6-phena
nthridinyl units attached by a short methylene spacer onto nitrogen at
oms of 7,16-diaza- and aza-l8-crown-6 rings have been prepared in high
yields. The fluoroionophores exhibited the ability to signal binding
of certain metal cations through the specific complexation induced shi
fts (CIS) of phenanthridine protons in H-1 NMR spectra as well as by t
he large intensity enhancements in fluorescence spectra. The X-ray str
ucture analysis of [1, K+(C2H4Cl2)] picrate complex revealed that K+ i
s nine-coordinated, using all donors from the diazacrown ring, one chl
orine atom from 1,2-dichloroethane solvent molecule and both nitrogen
donors from syn-oriented phenanthridine units.