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For a given cation, Pauling defined [2] the electrostatic bond strength to each coordinated anion as =, where z is the cation charge and ν is the cation coordination number. A stable ionic structure is arranged to preserve local electroneutrality , so that the sum of the strengths of the electrostatic bonds to an anion equals the charge on ...
Hydrogen bonds contribute to the stability of ion pairs with e.g. protonated ammonium ions, and with anions is formed by deprotonation as in the case of carboxylate, phosphate etc; then the association constants depend on the pH. Entropic driving forces for ion pairing (in absence of significant H-bonding contributions) are also found in ...
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 ...
For example, Na–Cl and Mg–O interactions have a few percent covalency, while Si–O bonds are usually ~50% ionic and ~50% covalent. Pauling estimated that an electronegativity difference of 1.7 (on the Pauling scale ) corresponds to 50% ionic character, so that a difference greater than 1.7 corresponds to a bond which is predominantly ionic.
Electrostatic attraction is not the only component of cation–π bonding. For example, 1,3,5-trifluorobenzene interacts with cations despite having a negligible quadrupole moment. While non-electrostatic forces are present, these components remain similar over a wide variety of arenes, making the electrostatic model a useful tool in predicting ...
A chemical bond is the association of atoms or ions to form molecules, crystals, and other structures. The bond may result from the electrostatic force between oppositely charged ions as in ionic bonds or through the sharing of electrons as in covalent bonds, or some combination of these effects.
A bond of higher bond order also exerts greater repulsion since the pi bond electrons contribute. [10] For example in isobutylene, (H 3 C) 2 C=CH 2, the H 3 C−C=C angle (124°) is larger than the H 3 C−C−CH 3 angle (111.5°). However, in the carbonate ion, CO 2− 3, all three C−O bonds are equivalent with angles of 120° due to resonance.
Griffith and Orgel used the electrostatic principles established in crystal field theory to describe transition metal ions in solution and used molecular orbital theory to explain the differences in metal-ligand interactions, thereby explaining such observations as crystal field stabilization and visible spectra of transition metal complexes.