General-base catalysed hydrolysis and nucleophilic substitution of activated amides in aqueous solutions

The reactivity of 1-benzoyl-3-phenyl-1,2,4-triazole (1a) was studied in the presence of a range of weak bases in aqueous solution. A change in mechanism is observed from general-base catalysed hydrolysis to nucleophilic substitution and general-base catalysed nucleophilic substitution. A slight tendency is also observed for the more hydrophobic general bases to show higher reactivity towards 1a. Aspartame is an effective nucleophile, possibly because nucleophilic substitution is subject to intramolecular general-base catalysis. A general conclusion derived from the present results is that unexpected rate effects can only be rationalised provided that the detailed reaction mechanisms are well understood. Copyright (C) 2003 John Wiley Sons, Ltd.</p

Classification of calorimetric titration plots for alkyltrimethylammonium and alkylpyridinium cationic surfactants in aqueous solutions

Calorimetric titration plots for deaggregation of micelles formed by alkylpyridinium and alkyltrimethylammonium surfactants are classified into three types, A, B and C, depending on the shape of the plot of the enthalpy of dilution as a function of surfactant concentration. For Type A plots the recorded heat of injection q changes sharply between two parts of the titration curve over which the recorded heats are effectively independent of the composition of the solution in the sample cell. For Type B plots, the change is less sharp and both parts of the plot show dependences of heat q on solution composition, a pattern accounted for in terms of solute-solute interactions. Type C plots are complicated, in that no sharp change in q is recorded, the complexity of the plots being accounted for in terms of micelle-monomer equilibria over a range of surfactant concentrations and related enthalpies of deaggregation

Thermal switch of oscillation frequency in belousov- zhabotinsky liquid marbles

© 2019 The Authors. External control of oscillation dynamics in the Belousov- Zhabotinsky (BZ) reaction is important for many applications including encoding computing schemes. When considering the BZ reaction, there are limited studies dealing with thermal cycling, particularly cooling, for external control. Recently, liquid marbles (LMs) have been demonstrated as a means of confining the BZ reaction in a system containing a solid-liquid interface. BZ LMs were prepared by rolling 50 ml droplets in polyethylene (PE) powder. Oscillations of electrical potential differences within the marble were recorded by inserting a pair of electrodes through the LM powder coating into the BZ solution core. Electrical potential differences of up to 100mV were observed with an average period of oscillation ca 44 s. BZ LMs were subsequently frozen to 218C to observe changes in the frequency of electrical potential oscillations. The frequency of oscillations reduced upon freezing to 11mHz cf. 23 mHz at ambient temperature. The oscillation frequency of the frozen BZ LM returned to 23 mHz upon warming to ambient temperature. Several cycles of frequency fluctuations were able to be achieved

Recombination of Geminate (OH,eaq-) Pairs in Concentrated Alkaline Solutions: Lack of Evidence For Hydroxyl Radical Deprotonation

Picosecond dynamics of hydrated electrons and hydroxyl radicals generated in 200 nm photodissociation of aqueous hydroxide and 400 nm (3-photon) ionization of water in concentrated alkaline solutions were obtained. No deprotonation of hydroxyl radicals was observed on sub-nanosecond time scale, even in 1-10 M KOH solutions. This result is completely at odds with the kinetic data for deprotonation of OH radical in dilute alkaline solutions. We suggest that the deprotonation of hydroxyl radical is slowed down dramatically in concentrated alkaline solutions.Comment: 12 pages; 2 figures; submitted to Chem. Phys. Let

Iodide-photocatalyzed reduction of carbon dioxide to formic acid with thiols and hydrogen sulfide

The photolysis of iodide anions promotes the reaction of carbon dioxide with hydrogen sulfide or thiols to quantitatively yield formic acid and sulfur or disulfides. The reaction proceeds in acetonitrile and aqueous solutions, at atmospheric pressure and room temperature by irradiation using a low-pressure mercury lamp. This transition-metal-free photocatalytic process for CO2 capture coupled with H2S removal may have been relevant as a prebiotic carbon dioxide fixation