When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Transition metal complexes of aldehydes and ketones

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Structure of [ZnBr 3 (η 1-acetone)] −. In monometallic complexes, aldehydes and ketones can bind to metals in either of two modes, η 1-O-bonded and η 2-C,O-bonded. These bonding modes are sometimes referred to sigma- and pi-bonded. These forms may sometimes interconvert.

  3. Acetone (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetone_(data_page)

    Structure and properties Index of refraction, n D: 1.3561 Dielectric constant, ε r: 20.7 ε 0 at 25 °C Bond strength? Bond length? ... vapor pressure of acetone ...

  4. Hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bond

    In the secondary structure of proteins, hydrogen bonds form between the backbone oxygens and amide hydrogens. When the spacing of the amino acid residues participating in a hydrogen bond occurs regularly between positions i and i + 4, an alpha helix is formed. When the spacing is less, between positions i and i + 3, then a 3 10 helix is formed.

  5. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.

  6. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    Both C-C central bonds are equivalent as well, with one hydrogen atom bonded to the central carbon atom (the C3 atom). Those two equivalencies are because there is a resonance between the four bonds in the O-C2-C3-C4-O linkage in the acetylacetonate anion, where the bond order of those four bonds is about 1.5.

  7. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    A hydrogen bond (H-bond), is a specific type of interaction that involves dipole–dipole attraction between a partially positive hydrogen atom and a highly electronegative, partially negative oxygen, nitrogen, sulfur, or fluorine atom (not covalently bound to said hydrogen atom). It is not a covalent bond, but instead is classified as a strong ...

  8. Metal aquo complex - Wikipedia

    en.wikipedia.org/wiki/Metal_aquo_complex

    Structure of an octahedral metal aquo complex. Chromium(II) ion in aqueous solution. Most aquo complexes are mono-nuclear, with the general formula [M(H 2 O) 6] n+, with n = 2 or 3; they have an octahedral structure. The water molecules function as Lewis bases, donating a pair of electrons to the metal ion and forming a dative covalent bond ...

  9. Agostic interaction - Wikipedia

    en.wikipedia.org/wiki/Agostic_interaction

    The term agostic is reserved to describe two-electron, three-center bonding interactions between carbon, hydrogen, and a metal. Two-electron three-center bonding is clearly implicated in the complexation of H 2, e.g., in W(CO) 3 (PCy 3) 2 H 2, which is closely related to the agostic complex shown in the figure. [8]