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Transcript
THE INTERPLAY OF COORDINATION CHEMISTRY AND SOLVATION IN
DESIGNING SELECTIVE SENSORS FOR TOXIC METALS AND OTHER IONIC
TARGETS. Konstantinos Kavallieratos, Department of Chemistry & Biochemistry,
Florida International University, 11200 SW 8th St., CP 326, Miami, FL 33199.
Despite their environmental health effects, efforts to design selective and practical
sensors for larger and relatively “softer” targets, with lower charge density, such as the
toxic metal species Pb(II) and Cd(II) and the anions ClO4- and NO3- still present
significant challenges. Solvent extraction from water into a less polar organic phase via
the formation of complexes with distinct optical or electrochemical properties presents
an opportunity for addressing selectivity issues, by combining the unique coordination
properties for each species (via ligand design), while taking advantage of more
favorable dehydration-resolvation energetics for these targets, compared to harder
more charge-dense ions (such as Ca2+) which are naturally present in high
concentrations and often compete for the ligand binding sites. Sulfonamides with
incorporated fluorophores have been shown previously to be effective ion-exchange
extractants. Herein we are expanding this approach with a variety of ligands and targets
and demonstrate the combined effects of coordination and solvent extraction principles
in sensor design.