Journal
ANALYTICAL CHEMISTRY
Volume 80, Issue 6, Pages 2084-2090Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ac702161c
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Funding
- NIBIB NIH HHS [1R01 EB005225-01] Funding Source: Medline
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Ionophore-doped sensor membranes exhibit greater selectivities and wider measuring ranges when they are prepared with noncoordinating matrixes. Since fluorous phases are the least polar and least polarizable liquid phases known, a fluorous phase was used for this work as the membrane matrix for a series of ionophore-based sensors to explore the ultimate limit of selectivity. Fluorous pH electrode membranes, each comprised of perfluoroperhydrophenanthrene, sodium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate, and one of four fluorophilic H+-selective ionophores were prepared. All the ionophores are highly fluorinated trialkylamines containing three electron withdrawing perfluoroalkyl groups shielded from the central nitrogen by alkyl spacers of varying lengths: [CF3(CF2)(7)(CH2)(3)](2)[CF3(CF2)(6)CH2]N, [CF3(CF2)(7)(CH2)(3)](2)(CF3CH2)N, [CF3(CF2)(7)(CH2)(3)](3)N, and [CF3(CF2)(7)(CH2)(5)](3)N. Their pK(a) values in the fluorous matrix are as high as 15.4 +/- 0.3, and the corresponding electrodes exhibit logarithmic selectivity coefficients for H+ over K+ as low as < -12.8. The pK(a) and selectivity follow the trends expected from the degree of shielding and the length of the perfluoroalkyl chains of the ionophores. These electrodes are the first fluorous ionophore-based sensors described in the literature. The selectivities of the sensor containing [CF3(CF2)(7)(CH2)(5)](3)N are not only greater than those of analogous sensors with nonfluorous membranes but were of the same magnitude as the best ionophore-based pH sensors ever reported.
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