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Updated: Jan 13, 2026

Determination of the Gas-phase Acidities of Oligopeptides
Published on: June 24, 2013
Salt Cluster With Surface Defect Shows Anomalous Acid-Base Chemistry
Jessica C Hartmann1, Jia Yang Lim2, Yiqi Sheng2
1Institut für Ionenphysik und Angewandte Physik, Universität Innsbruck, Technikerstraße 25, Innsbruck, 6020, Austria.
Abstract:
The acid displacement reaction of formic acid in sea-salt aerosols to release hydrogen chloride is an enigma in atmospheric chemistry: a weak acid transfers a proton to the conjugate base of a strong acid, reversing solution-phase acid-base chemistry. To shed light on this question, we compared the reactivity of formic acid with Na13Cl12 + and Na14Cl13 + under ultra-high vacuum conditions in a mass spectrometer. No reaction was observed with Na14Cl13 +, a known magic cluster that corresponds to a cubic section of the crystal lattice. Na13Cl12 +, which corresponds to the cubic section with a surface defect, reacts readily with release of hydrogen chloride and incorporation of formate into the salt structure. Quantum chemical calculations show that the reaction is substantially endothermic for the magic cluster. The surface defect, however, makes it exothermic. The reason lies in the induced fit of the formate ion in the Na13Cl11(HCOO)+ cluster. Its oxygen atoms interact with five sodium ions. In sum, these electrostatic interactions more than offset the 49 ± 13 kJ mol-1 difference in gas-phase acidity between hydrogen chloride and formic acid.
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Salts are ionic compounds composed of cations and anions, either of which may be capable of undergoing an acid or base ionization reaction with water. Aqueous salt solutions, therefore, may be acidic, basic, or neutral, depending on the relative acid-base strengths of the salt’s constituent ions. For example, dissolving the ammonium chloride in water results in its dissociation, as described by the equation:
Acids, Bases and Neutralization Reactions
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