enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Organoiron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiron_chemistry

    The rapid growth of organometallic chemistry in the 20th century can be traced to the discovery of ferrocene, a very stable compound which foreshadowed the synthesis of many related sandwich compounds. Ferrocene is formed by reaction of sodium cyclopentadienide with iron(II) chloride: 2 NaC 5 H 5 + FeCl 2 → Fe(C 5 H 5) 2 + 2 NaCl

  6. More O'Ferrall–Jencks plot - Wikipedia

    en.wikipedia.org/wiki/More_O'Ferrall–Jencks_plot

    These plots were first introduced in a 1970 paper by R. A. More O’Ferrall to discuss mechanisms of β-eliminations [2] and later adopted by W. P. Jencks in an attempt to clarify the finer details involved in the general acid-base catalysis of reversible addition reactions to carbon electrophiles such as the hydration of carbonyls.

  7. 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]

  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. Reference electrode - Wikipedia

    en.wikipedia.org/wiki/Reference_electrode

    The overall chemical reaction taking place in a cell is made up of two independent half-reactions, which describe chemical changes at the two electrodes. To focus on the reaction at the working electrode , the reference electrode is standardized with constant (buffered or saturated) concentrations of each participant of the redox reaction.