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  2. Agostic interaction - Wikipedia

    en.wikipedia.org/wiki/Agostic_interaction

    The interaction is the result of two electrons involved in the C−H bond interaction with an empty d-orbital of the transition metal, resulting in a three-center two-electron bond. [1] It is a special case of a C–H sigma complex. Historically, agostic complexes were the first examples of C–H sigma complexes to be observed spectroscopically ...

  3. C–H···O interaction - Wikipedia

    en.wikipedia.org/wiki/C–H···O_interaction

    Bond strength is less than 1 kcal/mol. In the case of aromatic C–H donors, C–H···O interactions are not linear due to influence of aromatic ring substituents near the interacting C-H group. [ 6 ] [ 7 ] If aromatic molecules involved in С–Н···О interaction belong to the group of polycyclic aromatic hydrocarbons , the strength of C ...

  4. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    This bond is a covalent, single bond, meaning that carbon shares its outer valence electrons with up to four hydrogens. This completes both of their outer shells, making them stable. [2] Carbon–hydrogen bonds have a bond length of about 1.09 Å (1.09 × 10 −10 m) and a bond energy of about 413 kJ/mol (see table below).

  5. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    In the figure each bond joins the central O atom with a negative charge (red) to an H atom with a positive charge (blue). The hydrogen fluoride , HF, molecule is polar by virtue of polar covalent bonds – in the covalent bond electrons are displaced toward the more electronegative fluorine atom.

  6. Chemical bond - Wikipedia

    en.wikipedia.org/wiki/Chemical_bond

    Hydrogen bonds of the form A--H•••B occur when A and B are two highly electronegative atoms (usually N, O or F) such that A forms a highly polar covalent bond with H so that H has a partial positive charge, and B has a lone pair of electrons which is attracted to this partial positive charge and forms a hydrogen bond.

  7. Hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bond

    In particular, intermolecular hydrogen bonding is responsible for the high boiling point of water (100 °C) compared to the other group-16 hydrides that have much weaker hydrogen bonds. [11] Intramolecular hydrogen bonding is partly responsible for the secondary and tertiary structures of proteins and nucleic acids.

  8. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    Lewis had suggested in 1916 that two atoms are held together in a chemical bond by sharing a pair of electrons. [18] When each atom contributed one electron to the bond, it was called a covalent bond. When both electrons come from one of the atoms, it was called a dative covalent bond or coordinate bond. The distinction is not very clear-cut.

  9. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Each bond consists of a pair of electrons, so if t is the total number of electrons to be placed and n is the number of single bonds just drawn, t−2n electrons remain to be placed. These are temporarily drawn as dots, one per electron, to a maximum of eight per atom (two in the case of hydrogen), minus two for each bond.