Poly(3-octylthiophene) as solid contact for ion-selective electrodes: contradictions and possibilities

The hydrophobic conductive polymer, poly(3-octylthiophene) (POT), is considered as uniquely suited to be used as an ion-to-electron transducer in solid contact (SC) ion-selective electrodes (ISEs). However, the reports on the performance characteristics of POT-based SC ISEs are quite conflicting. In this study, the potential sources of the contradicting results on the ambiguous drift and poor potential reproducibility of POT-based ISEs are compiled, and different approaches to minimize the drift and the differences in the standard potentials of POT-based SC ISEs are shown. To set the potential of the POT film, it has been loaded with a 7,7,8,8-tetracyanoquinodimethane (TCNQ/TCNQ^·?) redox couple. An approximately 1:1 TCNQ/TCNQ^·?ratio in the POT film has been achieved through potentiostatic control of the potential of the redox couple-loaded conductive polymer. It is hypothesized that once the POT film has a stable, highly reproducible redox potential, it will provide similarly stable and reproducible interfacial potentials between the POT film and the electron-conducting substrate and result in SC ISEs with excellent reproducibility and potential stability. Towards this goal, the potentials of Au, GC, and Pt electrodes with drop-cast POT film coatings were recorded in KCl solutions as a function of time. Some of the POT films were loaded with TCNQ and coated with a K⁺-selective membrane. The improvement in the potential stabilities and sensor-to-sensor reproducibility as a consequence of the incorporation of TCNQ in the POT film and the potentiostatic control of the TCNQ/TCNQ^·?ratio is reported.     

Concanavalin A electrochemical sensor based on the surface blocking principle at an ion-selective polymeric membrane

Microchimica Acta - We report on a new electrochemical sensor for Concanavalin A. It is based on blocking the surface of plasticized PVC membranes that were covalently modified with D-mannose using...     

Dynamic Formation of Noncovalent Calixsalen Aggregates

A procedure for studying “dynamic structural behavior” of large chiral macrocycles is presented. Ion mobility MS, diffusion‐ordered NMR spectroscopy (DOSY NMR), and optical rotation (OR) measurements, supported by calculations, are used together as effective complementary methods to study dynamic formation of noncovalent aggregates. It is shown that the monomer–dimer equilibrium is driven by π–π or CH–π interactions and controlled largely by the substitution pattern of the calixsalen skeleton.     

Polyphenols,L-Ascorbic Acid,and Antioxidant Activity in Wines from Rose Fruits (Rosa rugosa)

The aim of the present study was to determine the influence of the winemaking process on the antioxidant potential and content of phenolic compounds and L-ascorbic acid in wines from the fruits of Rosa rugosa. The results obtained in this study clearly indicate that the fruits of the Rosa rugosa are a desirable raw material for the production of fruit wine. The parameters of the technological process of producing wines from rose fruits had a diversified influence on the tested quality characteristics. Aged wines contained phenolics levels of 473–958 mg/100 mL GAE. The final concentrations of ascorbic acid ranged from 61 to 155 mg/100 mL for the different variants of the wine. Wines revealed high antioxidant activity in assay with DPPH. On the basis of the obtained results, it can be assumed that all the applied variants of the winemaking process are suitable for rose fruit wine. Each variant ensured at least the stability of the antioxidant capacity.     

The Solvent Effect on H2O2 Generation at Room Temperature Ionic Liquid|Water Interface

H₂O₂ is a versatile chemical and can be generated by the oxygen reduction reaction (ORR) in proton donor solution in molecular solvents or room temperature ionic liquids (IL). We investigated this reaction at interfaces formed by eleven hydrophobic ILs and acidic aqueous solution as a proton source with decamethylferrocene (DMFc) as an electron donor. H₂O₂ is generated in colorimetrically detectable amounts in biphasic systems formed by alkyl imidazolium hexafluorophosphate or tetraalkylammonium bis(trifluoromethylsulfonyl)imide ionic liquids. H₂O₂ fluxes were estimated close to liquid|liquid interface by scanning electrochemical microscopy (SECM). Contrary to the interfaces formed by hydrophobic electrolyte solution in a molecular solvent, H₂O₂ generation is followed by cation expulsion to the aqueous phase. Weak correlation between the H₂O₂ flux and the difference between DMFc/DMFc⁺ redox potential and 2 electron ORR standard potential indicates kinetic control of the reaction.