Fluorescent sensing arrays for cations and anions.

Array-based sensing methods can be used to distinguish sets of similar analytes, by using a number of non-specific or cross-reactive probes. Following subsequent statistical analysis, patterns or components can be isolated that can be used to unambiguously identify the specific analyte(s) present. Over the past two decades, various arrays for the identification of cations and anions have been reported. These often employ fluorescence methods, owing to good sensitivity and a versatile, easy to read output. The past few years have seen an increase in the number of such studies reported in the literature. This critical review will summarise this recent work, and identify the criteria required for a successful array system. In particular, it will focus on the different types of molecular structures that can be used, the breadth of ions that can be distinguished in a single array, the sensitivity and dynamic range to which they can be identified, and how successfully these aims have been met.

Effect of protic ionic liquid and surfactant structure on partitioning of polyoxyethylene non-ionic surfactants.

The partitioning constants and Gibbs free energies of transfer of poly(oxyethylene) n-alkyl ethers between dodecane and the protic ionic liquids (ILs) ethylammonium nitrate (EAN) and propylammonium nitrate (PAN) are determined. EAN and PAN have a sponge-like nanostructure that consists of interpenetrating charged and apolar domains. This study reveals that the ILs solvate the hydrophobic and hydrophilic parts of the amphiphiles differently. The ethoxy groups are dissolved in the polar region of both ILs by means of hydrogen bonds. The environment is remarkably water-like and, as in water, the solubility of the ethoxy groups in EAN decreases on warming, which underscores the critical role of the IL hydrogen-bond network for solubility. In contrast, amphiphile alkyl chains are not preferentially solvated by the charged or uncharged regions of the ILs. Rather, they experience an average IL composition and, as a result, partitioning from dodecane into the IL increases as the cation alkyl chain is lengthened from ethyl to propyl, because the IL apolar volume fraction increases. Together, these results show that surfactant dissolution in ILs is related to structural compatibility between the head or tail group and the IL nanostructure. Thus, these partitioning studies reveal parameters for the effective molecular design of surfactants in ILs.