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  2. Pyrithione - Wikipedia

    en.wikipedia.org/wiki/Pyrithione

    Pyrithione is the common name of an organosulfur compound with molecular formula C 5 H 5 NOS, chosen as an abbreviation of pyridinethione, and found in the Persian shallot. [4] It exists as a pair of tautomers, the major form being the thione 1-hydroxy-2(1H)-pyridinethione and the minor form being the thiol 2-mercaptopyridine N-oxide; it crystallises in the thione form. [5]

  3. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    Of the two half reactions, the oxidation step is the most demanding because it requires the coupling of 4 electron and proton transfers and the formation of an oxygen-oxygen bond. This process occurs naturally in plants photosystem II to provide protons and electrons for the photosynthesis process and release oxygen to the atmosphere, [ 1 ] as ...

  4. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Water-reactive substances [1] are those that spontaneously undergo a chemical reaction with water, often noted as generating flammable gas. [2] Some are highly reducing in nature. [ 3 ] Notable examples include alkali metals , lithium through caesium , and alkaline earth metals , magnesium through barium .

  5. Zinc pyrithione - Wikipedia

    en.wikipedia.org/wiki/Zinc_pyrithione

    Zinc pyrithione (or pyrithione zinc) is a coordination complex of zinc. It has fungistatic (inhibiting the division of fungal cells) and bacteriostatic (inhibiting bacterial cell division) properties and is used in the treatment of seborrhoeic dermatitis [ 2 ] and dandruff .

  6. Parikh–Doering oxidation - Wikipedia

    en.wikipedia.org/wiki/Parikh–Doering_oxidation

    The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively. [1] The procedure uses dimethyl sulfoxide (DMSO) as the oxidant and the solvent, activated by the sulfur trioxide pyridine complex (SO 3 •C 5 H 5 N) in the presence of triethylamine or diisopropylethylamine as base.

  7. Advanced oxidation process - Wikipedia

    en.wikipedia.org/wiki/Advanced_oxidation_process

    These reactive species can be applied in water and can oxidize virtually any compound present in the water matrix, often at a diffusion-controlled reaction speed. Consequently, ·OH reacts unselectively once formed and contaminants will be quickly and efficiently fragmented and converted into small inorganic molecules.

  8. Pyridine-N-oxide - Wikipedia

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

    The oxidation of pyridine can be achieved with a number of peracids including peracetic acid and perbenzoic acid. [3] Oxidation can also be effected by a modified Dakin reaction using a urea-hydrogen peroxide complex, [4] and sodium perborate [5] or, using methylrhenium trioxide (CH 3 ReO 3) as catalyst, with sodium percarbonate. [6]

  9. Water oxidation catalysis - Wikipedia

    en.wikipedia.org/wiki/Water_oxidation_catalysis

    Water oxidation catalysis (WOC) is the acceleration (catalysis) of the conversion of water into oxygen and protons: 2 H 2 O → 4 H + + 4 e − + O 2. Many catalysts are effective, both homogeneous catalysts and heterogeneous catalysts. The oxygen evolving complex in photosynthesis is the premier example. There is no interest in generating ...