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  2. 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.

  3. 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.

  4. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Molecular geometry influences several properties of a substance including its reactivity, polarity, phase of matter, color, magnetism and biological activity. [ 1 ] [ 2 ] [ 3 ] The angles between bonds that an atom forms depend only weakly on the rest of molecule, i.e. they can be understood as approximately local and hence transferable ...

  5. Ferrocenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Ferrocenecarboxaldehyde

    Ferrocenecarboxaldehyde is prepared by Vilsmeier-Haack reaction (formylation) using dimethylformamide and phosphorus oxychloride. [2] Diformylation does not occur readily. [3] According to X-ray crystallography ferrocenecarboxaldehyde adopts the expected sandwich structure exhibited by other ferrocenes. The formyl group is coplanar with its ...

  6. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A polar molecule has a net dipole as a result of the opposing charges (i.e. having partial positive and partial negative charges) from polar bonds arranged asymmetrically. Water (H 2 O) is an example of a polar molecule since it has a slight positive charge on one side and a slight negative charge on the other. The dipoles do not cancel out ...

  7. Ferrocenophanes - Wikipedia

    en.wikipedia.org/wiki/Ferrocenophanes

    Preparation of ferrocenophanes via dilithium ferrocene. An important starting compound for the production of ferrocenophanes is dilithioferrocene . This can be prepared simply via the reaction of ferrocene with n -butyllithium in the presence of tetramethylethylenediamine .

  8. 18-electron rule - Wikipedia

    en.wikipedia.org/wiki/18-electron_rule

    At picture below is shown the splitting of the d subshell in low-spin square-planar complexes. Examples are especially prevalent for derivatives of the cobalt and nickel triads. Such compounds are typically square-planar. The most famous example is Vaska's complex (IrCl(CO)(PPh 3) 2), [PtCl 4] 2−, and Zeise's salt [PtCl 3 (η 2-C 2 H 4)] −.

  9. Interference colour chart - Wikipedia

    en.wikipedia.org/wiki/Interference_colour_chart

    When using the chart, it is important to remember these tips: Isotropic and opaque (metallic) minerals cannot be identified this way. The stage of the microscope should be rotated until maximum colour is found, and therefore, the maximum birefringence. Each mineral, depending on the orientation, may not exhibit the maximum birefringence.