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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. Reference electrode - Wikipedia

    en.wikipedia.org/wiki/Reference_electrode

    Since the early 1960s ferrocene has been gaining acceptance as the standard reference for nonaqueous work for a number of reasons, and in 1984, IUPAC recommended ferrocene (0/1+) as a standard redox couple. [8] The preparation of the QRE electrode is simple, allowing for a fresh reference to be prepared with each set of experiments.

  4. 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.

  5. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    In chemistry, polarity is a separation of electric charge leading to a molecule or its chemical groups having an electric dipole moment, with a negatively charged end and a positively charged end. Polar molecules must contain one or more polar bonds due to a difference in electronegativity between the bonded atoms.

  6. Umpolung - Wikipedia

    en.wikipedia.org/wiki/Umpolung

    In organic chemistry, umpolung (German: [ˈʔʊmˌpoːlʊŋ]) or polarity inversion is the chemical modification of a functional group with the aim of the reversal of polarity of that group. [ 1 ] [ 2 ] This modification allows secondary reactions of this functional group that would otherwise not be possible. [ 3 ]

  7. 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]

  8. Ferrocenophanes - Wikipedia

    en.wikipedia.org/wiki/Ferrocenophanes

    Ferrocenophanes, also called ansa ferrocenes (from ansa: handle in greek), are organometallic compounds which are derived from ferrocene. They are a subset of ansa-metallocenes in which the metal is iron. In this compound class, the cyclopentadienyl ligands of the ferrocene are connected by one or more bridging groups. This hinders the rotation ...

  9. 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.