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  2. Sulfonate - Wikipedia

    en.wikipedia.org/wiki/Sulfonate

    The sulfonate ion. In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.

  3. Methanesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_acid

    Methanesulfonic acid (MsOH, MSA) or methanesulphonic acid (in British English) is an organosulfuric, colorless liquid with the molecular formula CH 3 SO 3 H and structure H 3 C−S(=O) 2 −OH.

  4. Sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonic_acid

    General structure of a sulfonic acid with the functional group indicated in blue. In organic chemistry, sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(=O) 2 −OH, where R is an organic alkyl or aryl group and the S(=O) 2 (OH) group a sulfonyl hydroxide. [1]

  5. Benzenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonic_acid

    Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.

  6. Silver trifluoromethanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Silver_trifluoromethanes...

    Toggle the table of contents. Silver trifluoromethanesulfonate. 9 languages. ... It is a reagent used in the synthesis of organic and inorganic triflates. Synthesis

  7. Trimethylsilyl trifluoromethanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_trifluorome...

    Toggle the table of contents. Trimethylsilyl trifluoromethanesulfonate. ... TMSOTf is also a useful reagent to replace metal-halogen bonds with a covalent M-O(SO2CF3 ...

  8. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    Many method have been developed for introducing sulfonate groups aside from direction sulfonation. A classic named reaction is the Piria reaction (Raffaele Piria, 1851) in which nitrobenzene is treated with a metal bisulfite forming an aminosulfonic acid as a result of combined nitro group reduction and sulfonation. [2] [5] [6] The Piria reaction

  9. ABTS - Wikipedia

    en.wikipedia.org/wiki/ABTS

    Under these conditions, the sulfonate groups are fully deprotonated and the mediator exists as a dianion. ABTS –· + e – → ABTS 2– E° ′ = 0.67 V vs SHE ABTS + e – → ABTS –· E° ′ = 1.08 V vs SHE [1] This compound is chosen because the enzyme facilitates the reaction with hydrogen peroxide, turning it into a green and soluble ...