Evidence for the competition between long-range electron transfer across self-assembled monolayers (SAMs) and incorporation of the redox probe into the film is reported for the electroreduction of Ru(NH(3)) at hydroxyl- and carboxylic-acid-terminated SAMs on a mercury electrode, by using electrochemical techniques that operate at distinct time scales. Two limiting voltammetric behaviors are observed, consistent with a diffusion control of the redox process at mercaptophenol-coated electrodes and a kinetically controlled electron transfer reaction in the presence of neutral HS-(CH(2))(10)-COOH and HS-(CH(2))(n)()-CH(2)OH (n = 3, 5, and 10) SAMs. The monolayer thickness dependence of the standard heterogeneous electron transfer rate constant shows that the electron transfer plane for the reduction of Ru(NH(3)) at hydroxyl-terminated SAMs is located outside the film | solution interface at short times. However, long time scale experiments provide evidence for the occurrence of potential-induced gating of the adsorbed structure in some of the monolayers studied, which takes the form of a chronoamperometric spike. Redox probe permeation is shown to be a kinetically slow process, whose activation strongly depends on redox probe concentration, applied potential, and chemical composition of the intervening medium. The obtained results reveal that self-assembled monolayers made of mercaptobutanol and mercaptophenol preserve their electronic barrier properties up to the reductive desorption potential of a fully grown SAM, whereas those of mercaptohexanol, mercaptoundecanol, and mercaptoundecanoic acid undergo an order/disorder transition below a critical potential, which facilitates the approach of the redox probe toward the electrode surface.
Reorientation of thiols during their 2D self-assembly is well established; however, little is known about its energetics and the factors that control its onset. We have developed a new strategy to determine the critical reorientational surface concentration (crsc) of thiols at the substrate/solution interface, which makes use of a cathodic stripping protocol. Its application to distinct homologous series of alkylthiols shows that the magnitude of the crsc and its variation with the molecular size is strongly dependent on the nature of the terminal group. Methyl-terminated alkylthiols reorient close to the saturation coverage of the lying-down phase, thus following their molecular size trend; whereas reorientation of alkylthiols bearing a negatively charged end group starts well below the monolayer coverage of the lying-down phase, with its onset being almost independent of the molecular size. Hydroxy-terminated alkylthiols show an intermediate behavior. A theoretical approach is developed to determine the reorientation equilibrium constant from the crsc value. The standard free energy of reorientation has been found to vary linearly with the alkyl chain length, and to increase upon replacing the terminal methyl group by a negatively charged one. A quantitative correlation between the reorientation equilibrium constant and the hydrophobicity of the molecule has been established. Overall, these findings have allowed us to disentangle the role of steric and energetic factors in the onset of the reorientation process of alkylthiols, demonstrating that their interplay can be finely tuned by varying either the alkyl chain length or the nature of the terminal group.
The volatile congener analysis of 52 commercialized whiskeys (24 samples of single malt Scotch whiskey, 18 samples of bourbon whiskey, and 10 samples of Irish whiskey) was carried out by gas chromatography/mass spectrometry after liquid-liquid extraction with dichloromethane. Pattern recognition procedures were applied for discrimination of different whiskey categories. Multivariate data analysis includes linear discriminant analysis (LDA), k nearest neighbors (KNN), soft independent modeling of class analogy (SIMCA), procrustes discriminant analysis (PDA), and artificial neural networks techniques involving multilayer perceptrons (MLP) and probabilistic neural networks (PNN). Classification rules were validated by considering the number of false positives (FPs) and false negatives (FNs) of each class associated to the prediction set. Artificial neural networks led to the best results because of their intrinsic nonlinear features. Both techniques, MLP and PNN, gave zero FPs and zero FNs for all of the categories. KNN is a nonparametric method that also provides zero FPs and FNs for every class but only when selecting K = 3 neighbors. PDA produced good results also (zero FPs and FNs always) but only by selecting nine principal components for class modeling. LDA shows a lesser classification performance, because of the building of linear frontiers between classes that does not apply in many real situations. LDA led to one FP for bourbons and one FN for scotches. The worse results were obtained with SIMCA, which gave a higher number of FPs (five for both scotches and bourbons) and FNs (six for scotchs and two for bourbons). The possible cause of these findings is the strong influence of class inhomogeneities on the SIMCA performance. It is remarkable that in any case, all of the methodologies lead to zero FPs and FNs for the Irish whiskeys.
A theoretical description of ionic micellar solutions, which are considered as a mixture of two fully dissociated electrolytes with a common ion, is proposed. The solution is modeled within the framework of an improved primitive model, in which the solution permittivity as well as the charge and size of the solutes are allowed to vary with surfactant concentration. The MSA theory is used to estimate the electrostatic interactions, and the Carnahan-Starling approximation is employed to evaluate the hard-sphere contributions to the osmotic and activity coefficients. The experimental osmotic coefficients of sodium dodecyl sulfate (SDS) solutions are reproduced by using a value of 1.9 + 4CT nm for the micellar radius, CT being the total surfactant molar concentration. This is the only adjustable parameter in the theory, and the agreement with published estimations of the size of SDS micelles is excellent.
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