Mild, General, and Regioselective Synthesis of 2-Aminopyridines from Pyridine N-Oxides via N-(2-Pyridyl)pyridinium Salts

A synthesis of 2-aminopyridines from pyridine N-oxides via their corresponding N-(2-pyridyl)pyridinium salts has been demonstrated and investigated. The reaction sequence features a highly regioselective conversion of the N-oxide into its pyridinium salt followed by hydrolytic decomposition of the pyridinium moiety to furnish the 2-aminopyridine product. The method is compatible with a wide range of functional groups, is scalable, and features inexpensive reagents. 15N-labeling results gave products consistent with a Zincke reaction mechanism.

Reasons for Reduced Moisture Resistance of Sulfur-Extended Asphalt Concrete

The paper presents the results of a study of the mechanism for reducing the moisture resistance of sulfur-extended asphalt concrete. It is shown that a decrease in moisture resistance occurs due to the occurrence of chemical and physical processes. At the same time, it was found that during the manufacture of sulfur-bitumen composites, toxic gases H2S and SO2 are formed, which are capable of interacting with a mineral filler, as well as the interaction of sulfur with a mineral powder with the formation of sulfur-containing water-soluble salts, the extraction of which leads to a decrease in the moisture resistance of sulfur-bitumen materials. The change in the rate of leaching of these substances from the composite is due to the physical process caused by the crystallization of sulfur and the formation of a capillary structure, which significantly increases the rate of leaching of calcium and magnesium salts, which are products of dissolution or hydrolytic decomposition of water-soluble products of the interaction of sulfur, H2S and SO2 gases with calcium and magnesium carbonates. The intensity of chemical and physical processes intensifies with an increase in the amount of sulfur in sulfur-bitumen materials.

Effect of hydrogen, and vapors of water and organic compounds on the structure of Sr2CuO3

The effect of hydrogen, and vapors of water and the simplest organic compounds of various classes on the structure of strontium orthocuprate (Sr2CuO3) in the temperature range of 150–300 °C has been investigated. At temperatures up to 200 °C, hydrogen and water are embedded in the structure of Sr2CuO3 from the annealing atmosphere. Under these conditions, organic compounds are oxidized to form water followed by hydration of Sr2CuO3. It has been revealed that Sr2CuO3 is a catalyst for oxidation reactions. Water absorption > 2 wt.% provokes hydrolytic decomposition of Sr2CuO3 with the formation of strontium hydroxide and copper-richer cuprates (SrCuO2 and SrCu2O3). At a temperature of 300 °C, organic compounds partially reduce copper, which is also the cause of the decomposition of Sr2CuO3.

A Series of Cube-Shaped Polyoxoniobates Encapsulating Octahedral Cu12XmOn Clusters With Hydrolytic Decomposition for Chemical Warfare Agents

This study reported a series of cube-shaped polyoxoniobates, {MCu12O8)(Cu12XmOn)(Nb7(OH)O21)8} [M = Nb(1, 2), Ln3+(3), X = I(1, m = 3, n = 3; 2, m = 5, n = 1), Br(3, m = 5, n = 1)]. As the first octahedral Cu12XmOn cluster incorporated polyoxoniobate, the cube-shaped three-shell structure of {MCu12O8)(Cu12XmOn)(Nb7(OH)O21)8} polyanion contains a {MCu12O8} body-centered cuboctahedron, a {Cu12XmOn} octahedron and a {Cu12(Nb7(OH)O21)8} cube. Compounds 1, 2, 3 show effective catalytic activities for the hydrolytic decomposition of chemical warefare agent simulants.

Cyclophosphates, a new class of native phosphorus compounds, and some insights into prebiotic phosphorylation on early Earth

Cyclophosphates are a class of energy-rich compounds whose hydrolytic decomposition (ring opening) liberates energy that is sufficient for initiation of biomimetic phosphorylation reactions. Because of that, cyclophosphates might be considered as a likely source of reactive prebiotic phosphorus on early Earth. A major obstacle toward adoption of this hypothesis is that cyclophosphates have so far not been encountered in nature. We herein report on the discovery of these minerals in the terrestrial environment, at the Dead Sea basin in Israel. Cyclophosphates represent the most condensed phosphate species known in nature. A pathway for cyclophosphate geosynthesis is herein proposed, involving simple pyrolytic oxidation of terrestrial phosphides. Discovery of natural cyclophosphates opens new opportunities for modeling prebiotic phosphorylation reactions that resulted in the emergence of primordial life on our planet.