In this article, we will delve into the exciting world of Tetrakis(pyridine)silver(II) peroxydisulfate, exploring its many facets and providing a detailed analysis of its importance in today's society. Along the following lines, we will address its historical relevance, its impact in the professional field, its influence on popular culture and the challenges it faces today. Tetrakis(pyridine)silver(II) peroxydisulfate is a topic of great interest and its study will allow us to better understand its scope and the way in which it has shaped our reality. Join us on this tour of Tetrakis(pyridine)silver(II) peroxydisulfate and discover everything this theme has to offer.
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Names | |
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Other names
Tetrakis(pyridine)silver(II) persulfate, Tetrakis(pyridine)silver(II) peroxodisulfate
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
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Properties | |
C20H20N4AgS2O8 | |
Molar mass | 616.39 g·mol−1 |
Appearance | orange solid |
insoluble | |
Structure | |
Square planar | |
Hazards | |
Flash point | 20 °C (68 °F; 293 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Tetrakis(pyridine)silver(II) peroxydisulfate is a chemical compound which contains silver in the rare oxidation state of +2.
The salt can be easily prepared by oxidizing a soluble silver salt with excess potassium peroxydisulfate in aqueous pyridine solution, where upon the product precipitates out almost quantitatively.[1]
Since the Ag2+ ion has a d9 configuration, the salt is paramagnetic.[1]
The compound is in the form of non-hygroscopic orange granulate. It is stable in the air for several days when stored away from light, and is stable up to several months if dried in vacuo over potassium hydroxide, decomposing into a white paste. Its stability can be attributed to its insolubility in both polar and non-polar solvents.
The compound decomposes at 137 °C. It dissolves in concentrated nitric acid without reduction, and is converted to the black silver(I,III) oxide in aqueous sodium hydroxide solution.[1]
It is a powerful oxidizing agent, and is illustrated by the fact that it oxidizes Mn2+ ions to permanganates. When the pyridine ligands were removed, the transient square planar 2+ remains, which spontaneously oxidizes water to oxygen.[2]
The complex ion can easily oxidize alcohol, aldehyde and amine, and capable of decarboxylating α-hydroxycarboxylic acids and phenylacetic acids to give the corresponding carbonyl compounds.[3] Benzylic C-H bonds are oxidatively converted to carbonyl groups:[3]
Aromatic thiols and allylaryl thioethers are oxidized to arylsulfonic acids, which gives an alternative route to produce arylsulfonic acids with mild conditions.[3]
As the compound contains the peroxydisulfate ion as the counter anion, this compound should be treated as an explosive even though its explosive properties were not well established. The complex also releases tiny amounts of pyridine vapor which is a possible carcinogen.