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  2. Acetylferrocene - Wikipedia

    en.wikipedia.org/wiki/Acetylferrocene

    Acetylferrocene is the organoiron compound with the formula (C 5 H 5)Fe(C 5 H 4 COCH 3). It consists of ferrocene substituted by an acetyl group on one of the cyclopentadienyl rings. It is an orange, air-stable solid that is soluble in organic solvents.

  3. Ferrocene - Wikipedia

    en.wikipedia.org/wiki/Ferrocene

    Ferrocene is an organometallic compound with the formula Fe(C 5 H 5) 2.The molecule is a complex consisting of two cyclopentadienyl rings sandwiching a central iron atom. It is an orange solid with a camphor-like odor that sublimes above room temperature, and is soluble in most organic solvents.

  4. Ferrocenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Ferrocenecarboxaldehyde

    Ferrocenecarboxaldehyde, owing to the versatility of the formyl group, is a precursor to many ferrocene-modified compounds. With a Wittig reagent, it converts to vinylferrocene and related derivatives. [5] With primary amines, ferrocenecarboxaldehyde condenses to give imines. The azomethine derivative undergoes 1,3-cycloaddition to C 60. [6]

  5. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    An increase in solvent polarity decreases the rates of reactions where there is less charge in the activated complex in comparison to the starting materials; A change in solvent polarity will have little or no effect on the rates of reaction when there is little or no difference in charge between the reactants and the activated complex. [6]

  6. Taft equation - Wikipedia

    en.wikipedia.org/wiki/Taft_equation

    where ⁡ is the ratio of the rate of the substituted reaction compared to the reference reaction, ρ* is the sensitivity factor for the reaction to polar effects, σ* is the polar substituent constant that describes the field and inductive effects of the substituent, δ is the sensitivity factor for the reaction to steric effects, and E s is ...

  7. Polarization (electrochemistry) - Wikipedia

    en.wikipedia.org/wiki/Polarization...

    In electrochemistry, polarization is a collective term for certain mechanical side-effects (of an electrochemical process) by which isolating barriers develop at the interface between electrode and electrolyte. These side-effects influence the reaction mechanisms, as well as the chemical kinetics of corrosion and metal deposition.

  8. Sandwich compound - Wikipedia

    en.wikipedia.org/wiki/Sandwich_compound

    Space-filling model of ferrocene, the archetypal sandwich compound. In organometallic chemistry, a sandwich compound is a chemical compound featuring a metal bound by haptic, covalent bonds to two arene (ring) ligands. The arenes have the formula C n H n, substituted derivatives (for example C n (CH 3) n) and heterocyclic derivatives (for ...

  9. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    1. The change in the solvent polarity will influence the rate less than the equilibrium. 2. The rate constants will be characterized by opposite effect on the polarity: k 1 will slightly decrease with the increase of E T (30), and k −1 will increase under the same conditions. 3. The effect on k −1 will be larger than on k 1. [8]