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The charge of the resulting ions is a major factor in the strength of ionic bonding, e.g. a salt C + A − is held together by electrostatic forces roughly four times weaker than C 2+ A 2− according to Coulomb's law, where C and A represent a generic cation and anion respectively. The sizes of the ions and the particular packing of the ...
Ionic potential is the ratio of the electrical charge (z) to the radius (r) of an ion. [1]= = As such, this ratio is a measure of the charge density at the surface of the ion; usually the denser the charge, the stronger the bond formed by the ion with ions of opposite charge.
An electrostatic potential map of the nitrate ion (2NO − 3). The 3-dimensional shell represents a single arbitrary isopotential. Polyatomic and molecular ions are often formed by the gaining or losing of elemental ions such as a proton, H +, in neutral molecules.
For example, from Fe 2+ + 2 e − ⇌ Fe(s) (–0.44 V), the energy to form one neutral atom of Fe(s) from one Fe 2+ ion and two electrons is 2 × 0.44 eV = 0.88 eV, or 84 907 J/(mol e −). That value is also the standard formation energy (∆ G f °) for an Fe 2+ ion, since e − and Fe( s ) both have zero formation energy.
Figure 1. Example of salt bridge between amino acids glutamic acid and lysine demonstrating electrostatic interaction and hydrogen bonding. In chemistry, a salt bridge is a combination of two non-covalent interactions: hydrogen bonding and ionic bonding (Figure 1).
The electrostatic interaction model of ions in solids has thus been extended to a point multipole concept that also includes higher multipole moments like dipoles, quadrupoles etc. [8] [9] [10] These concepts require the determination of higher order Madelung constants or so-called electrostatic lattice constants.
The bond then results from electrostatic attraction between the positive and negatively charged ions. Ionic bonds may be seen as extreme examples of polarization in covalent bonds. Often, such bonds have no particular orientation in space, since they result from equal electrostatic attraction of each ion to all ions around them.
Practically, this allows trends to be predicted qualitatively based on visual representations of electrostatic potential maps for a series of arenes. 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.