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  2. Organoaluminium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoaluminium_chemistry

    The Al–C bond is polarized such that the carbon is highly basic. Acids react to give alkanes. For example, alcohols give alkoxides: AlR' 3 + ROH → 1/n (R' 2 Al−OR) n + R'H. A wide variety of acids can be employed beyond the simple mineral acids. Amines give amido derivatives.

  3. Aluminium(I) nucleophiles - Wikipedia

    en.wikipedia.org/wiki/Aluminium(I)_nucleophiles

    Each aluminium(I) atom is supported by two amido nitrogen atoms and one ethereal oxygen atom of the ligand, formally having a filled octet. The two monomeric units are joined by electrostatic interactions between the positively charged potassium cations and the electron clouds of the Dipp (diisopropylphenyl) substituents.

  4. Lewis acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Lewis_Acid_Catalysis

    Common Lewis acid catalysts are based on main group metals such as aluminum, boron, silicon, and tin, as well as many early (titanium, zirconium) and late (iron, copper, zinc) d-block metals. The metal atom forms an adduct with a lone-pair bearing electronegative atom in the substrate, such as oxygen (both sp 2 or sp 3), nitrogen, sulfur, and ...

  5. Transition metal carboxylate complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carboxyl...

    Carboxylates bind to single metals by one or both oxygen atoms, the respective notation being κ 1 - and κ 2-.In terms of electron counting, κ 1-carboxylates are "X"-type ligands, i.e., a pseudohalide-like. κ 2-carboxylates are "L-X ligands", i.e. resembling the combination of a Lewis base (L) and a pseudohalide (X).

  6. Transmetalation - Wikipedia

    en.wikipedia.org/wiki/Transmetalation

    During transmetalation the metal-carbon bond is activated, leading to the formation of new metal-carbon bonds. [2] Transmetalation is commonly used in catalysis, synthesis of main group complexes, and synthesis of transition metal complexes.

  7. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    Homologation reactions like the Kowalski ester homologation [3] provide simple examples of insertion process in organic synthesis. In the Arndt-Eistert reaction, [4] [5] a methylene unit is inserted into the carboxyl-carbon bond of carboxylic acid to form the next acid in the homologous series.

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  9. Aluminium compounds - Wikipedia

    en.wikipedia.org/wiki/Aluminium_compounds

    Aluminium's electropositive behavior, high affinity for oxygen, and highly negative standard electrode potential are all more similar to those of scandium, yttrium, lanthanum, and actinium, which have ds 2 configurations of three valence electrons outside a noble gas core: aluminium is the most electropositive metal in its group. [1] Aluminium ...