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  2. Pyridinium perbromide - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_perbromide

    Pyridinium perbromide (also called pyridinium bromide perbromide, pyridine hydrobromide perbromide, or pyridinium tribromide) is an organic chemical composed of a pyridinium cation and a tribromide anion. It can also be considered as a complex containing pyridinium bromide—the salt of pyridine and hydrogen bromide—with an added bromine (Br ...

  3. Tribromide - Wikipedia

    en.wikipedia.org/wiki/Tribromide

    Tribromide is the anion with the chemical formula Br 3 −, or salts containing it: . Tetrabutylammonium tribromide; Tetrabromophosphonium tribromide; Pyridinium perbromide; Sodium and potassium tribromides can be prepared by reacting NaBr or KBr with aqueous bromine.

  4. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    Pyridinium refers to the cation [C 5 H 5 NH] +. It is the conjugate acid of pyridine . Many related cations are known involving substituted pyridines, e.g. picolines, lutidines, collidines.

  5. Pyridine-N-oxide - Wikipedia

    en.wikipedia.org/wiki/Pyridine-N-oxide

    Pyridine-N-oxide is the heterocyclic compound with the formula C 5 H 5 NO. This colourless, hygroscopic solid is the product of the oxidation of pyridine. It was originally prepared using peroxyacids as the oxidising agent. The compound is used infrequently as an oxidizing reagent in organic synthesis. [1]

  6. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.

  7. Methylpyridinium - Wikipedia

    en.wikipedia.org/wiki/Methylpyridinium

    Methylpyridinium is prepared by treating pyridine with dimethylsulfate: [2]. C 5 H 5 N + (CH 3 O) 2 SO 2 → [C 5 H 5 NCH 3] + CH 3 OSO − 3. It is found in some coffee products. [3] It is not present in unroasted coffee beans, but is formed during roasting from its precursor chemical, trigonelline. [3]

  8. Pyrophoricity - Wikipedia

    en.wikipedia.org/wiki/Pyrophoricity

    The creation of sparks from metals is based on the pyrophoricity of small metal particles, and pyrophoric alloys are made for this purpose. [2] Practical applications include the sparking mechanisms in lighters and various toys, using ferrocerium; starting fires without matches, using a firesteel; the flintlock mechanism in firearms; and spark testing ferrous metals.

  9. Bromoantimonates - Wikipedia

    en.wikipedia.org/wiki/Bromoantimonates

    Although antimony tribromide is known, SbBr 5 on its own does not exist, despite the existence of SbBr − 6. [1] Compounds containing both Sb(III) and Sb(V) are mixed valence compounds. The antimony can be linked into chains, (which are called one-dimensional as it is like a line), or in pairs as Sb 2 or singly as Sb (which are called zero ...