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  2. Electron affinity - Wikipedia

    en.wikipedia.org/wiki/Electron_affinity

    The electron affinity of molecules is a complicated function of their electronic structure. For instance the electron affinity for benzene is negative, as is that of naphthalene, while those of anthracene, phenanthrene and pyrene are positive. In silico experiments show that the electron affinity of hexacyanobenzene surpasses that of fullerene. [5]

  3. Electron affinity (data page) - Wikipedia

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

    Electron affinity can be defined in two equivalent ways. First, as the energy that is released by adding an electron to an isolated gaseous atom. The second (reverse) definition is that electron affinity is the energy required to remove an electron from a singly charged gaseous negative ion.

  4. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The cluster must therefore have a higher electron affinity for the electron than iodine and therefore the aluminium cluster is called a superhalogen (i.e., the vertical electron detachment energies of the moieties that make up the negative ions are larger than those of any halogen atom). [45] The cluster component in the Al 13 I −

  5. Properties of nonmetals (and metalloids) by group - Wikipedia

    en.wikipedia.org/wiki/Properties_of_nonmetals...

    Chemically, the nonmetals mostly have higher ionisation energies, higher electron affinities (nitrogen and the noble gases have negative electron affinities) and higher electronegativity values [n 1] than metals noting that, in general, the higher an element's ionisation energy, electron affinity, and electronegativity, the more nonmetallic ...

  6. Halogen bond - Wikipedia

    en.wikipedia.org/wiki/Halogen_bond

    Although all halogens can theoretically participate in halogen bonds, the σ-hole shrinks if the electron cloud in question polarizes poorly or the halogen is so electronegative as to polarize the associated σ-bond. [3] [9] Consequently halogen-bond propensity follows the trend [10] [Note 1] F < Cl < Br < I.

  7. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    In Organic chemistry, the inductive effect in a molecule is a local change in the electron density due to electron-withdrawing or electron-donating groups elsewhere in the molecule, resulting in a permanent dipole in a bond. [1] It is present in a σ (sigma) bond, unlike the electromeric effect which is present in a π (pi) bond.

  8. Electronegativity - Wikipedia

    en.wikipedia.org/wiki/Electronegativity

    The Mulliken electronegativity can only be calculated for an element whose electron affinity is known. Measured values are available for 72 elements, while approximate values have been estimated or calculated for the remaining elements. The Mulliken electronegativity of an atom is sometimes said to be the negative of the chemical potential. [14]

  9. Periodic trends - Wikipedia

    en.wikipedia.org/wiki/Periodic_trends

    The energy released when an electron is added to a neutral gaseous atom to form an anion is known as electron affinity. [15] Trend-wise, as one progresses from left to right across a period , the electron affinity will increase as the nuclear charge increases and the atomic size decreases resulting in a more potent force of attraction of the ...