Mmg. Antonisse et al., NEUTRAL ANION RECEPTORS - SYNTHESIS AND EVALUATION AS SENSING MOLECULES IN CHEMICALLY-MODIFIED FIELD-EFFECT TRANSISTORS, Journal of organic chemistry, 62(26), 1997, pp. 9034-9038
A new class of anion selective receptors is based on the neutral urany
lsalophene building block as Lewis acidic binding site. Additional hyd
rogen bond accepting or donating moieties near the anion binding site
offer the possibility of varying the binding selectivity. Field effect
transistors chemically modified with such receptors exhibit anion sel
ectivities that strongly deviate from the classical Hofmeister series
favoring phosphate or fluoride anions, depending on the structure of t
he uranylsalophenes. The phosphate selective chemically modified field
effect transistors (CHEMFETs) detect phosphate with high selectivity
over much more lipophilic anions, such as nitrate (log K-H2PO4,NO3(Pot
) = -1.3), at [H2PO4-] greater than or equal to 6.3 x 10(-4) M. CHEMFE
Ts modified with salophenes with amido substituents result in a high f
luoride selectivity; even in the presence of 0.1 M chloride, fluoride
can be detected at [F-] greater than or equal to 6 x 10(-4) M (log K-F
,Cl(Pot) = -2.0).