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  2. Manganese(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Manganese(II)_acetate

    The anhydrous material and dihydrate Mn(CH 3 CO 2) 2 ·2H 2 O are coordination polymers. The dihydrate has been characterized by X-ray crystallography. Each Mn(II) center is surrounded by six oxygen centers provided by aquo ligands and acetates. Subunit of the structure of the dihydrate of manganese(II) acetate. [5]

  3. Manganese (III) acetate - Wikipedia

    en.wikipedia.org/wiki/Manganese(III)_acetate

    Manganese triacetate has been used as a one-electron oxidant.It can oxidize alkenes via addition of acetic acid to form lactones. [3]This process is thought to proceed via the formation of a •CH 2 CO 2 H radical intermediate, which then reacts with the alkene, followed by additional oxidation steps and finally ring closure. [1]

  4. Manganese-mediated coupling reactions - Wikipedia

    en.wikipedia.org/wiki/Manganese-mediated...

    Manganese acetate itself can effect the second oxidation of resonance-stabilized adduct radicals to carbocations 5; [5] unstabilized radicals undergo further transformations before reacting with Mn(OAc) 3. Atom transfer from another molecule of substrate may generate saturated compound 3. Adduct radicals or carbocations may undergo ligand ...

  5. Magnesium acetate - Wikipedia

    en.wikipedia.org/wiki/Magnesium_acetate

    2 CH 3 COOH + Mg(OH) 2 → (CH 3 COO) 2 Mg + 2 H 2 O. Magnesium carbonate suspended in distilled water with 20% acetic acid solution. [8] 2 CH 3 COOH + MgCO 3 → Mg(CH 3 COO) 2 + CO 2 + H 2 O. Reacting metallic magnesium with acetic acid dissolved in dry benzene causes magnesium acetate to form along with the release of hydrogen gas. [9] Mg ...

  6. Copper(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Copper(II)_acetate

    In the Eglinton reaction Cu 2 (OAc) 4 is used to couple terminal alkynes to give a 1,3-diyne: [13] [14] Cu 2 (OAc) 4 + 2 RC≡CH → 2 CuOAc + RC≡CC≡CR + 2 HOAc. The reaction proceeds via the intermediacy of copper(I) acetylides, which are then oxidized by the copper(II) acetate, releasing the acetylide radical. A related reaction ...

  7. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    In organic chemistry, the acetoxy group (abbr. AcO or OAc; IUPAC name: acetyloxy [1]), is a functional group with the formula −OCOCH 3 and the structure −O−C(=O)−CH 3. As the -oxy suffix implies, it differs from the acetyl group (−C(=O)−CH 3) by the presence of an additional oxygen atom. The name acetoxy is the short form of acetyl-oxy.

  8. Bis(triphenylphosphineoxide) manganese(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Bis(triphenylphosphine...

    A convenient synthesis starts from Mn(OAc) 2, trimethylsilylchloride, and potassium permanganate. [3] [MnCl 3 (OPPh 3) 2] can be used as a starting material in coordination chemistry. [3] [MnCl 3 (OPPh 3) 2] can also be used as a stoichiometric reagent in alkene dihalogenation reactions. [3]

  9. Antimony(III) acetate - Wikipedia

    en.wikipedia.org/wiki/Antimony(III)_acetate

    Sb 2 O 3 + 3 C 4 H 6 O 32 Sb(CH 3 CO 2) 3. ... acetate has been determined by X-ray crystallography. It consists of discrete Sb(OAc) 3 monomers with monodentate ...