Information about Van Der Waals Bonding

The van der Waals equation is an equation of state that can be derived from a special form of the potential between a pair of molecules (hard-sphere repulsion and R''^-6 van der Waals attraction).

In chemistry and physics, the name van der Waals force is sometimes used as a synonym for the totality of non-covalent forces (also known as intermolecular forces). These forces, which act between stable molecules, are weak compared to those appearing in chemical bonding. Historically, the use of the name for the total force is correct, because the Dutch physicist J. D. van der Waals, who lent his name to these forces, considered both the repulsive and the attractive component of the intermolecular force.

Unfortunately, there is no strict convention when considering the definition of Van der Waals force. Some texts consider only the attractive component of the intermolecular potential as the Van der Waals force. Other texts designate only a certain part of the attraction as the Van der Waals force.

To explain this, we refer to the article on intermolecular forces, where it is discussed that an intermolecular force has four major contributions. In general an intermolecular potential has a repulsive part, prohibiting the collapse of molecular complexes, and an attractive part. The attractive part, in turn, consists of three distinct contributions

(i) The electrostatic interactions between charges (in the case of molecular ions), dipoles (in the case of molecules without inversion center), quadrupoles (all molecules with symmetry lower than cubic), and in general between permanent multipoles. The electrostatic interaction is sometimes called Keesom interaction or Keesom force after Willem Hendrik Keesom.

(ii) The second source of attraction is induction (also known as polarization), which is the interaction between a permanent multipole on one molecule with an induced multipole on another. This interaction is sometimes measured in debyes after Peter J.W. Debye.

(iii) The third attraction is usually named after London who himself called it dispersion. This is the only attraction experienced by noble gas atoms, but it is operative between any pair of molecules, irrespective of their symmetry.

Returning to nomenclature: some texts mean by the Van der Waals force the totality of forces (including repulsion), others mean all the attractive forces (and then sometimes distinguish Van der Waals-Keesom, Van der Waals-Debye, and Van der Waals-London), and, finally some use the term "Van der Waals force" solely as a synonym for the London/dispersion force. So, if you come across the term "Van der Waals force", it is important to ascertain to which school of thought the author belongs.

All intermolecular/Van der Waals forces are anisotropic (except those between two noble gas atoms), which means that they depend on the relative orientation of the molecules. The induction and dispersion interactions are always attractive, irrespective of orientation, but the electrostatic interaction changes sign upon rotation of the molecules. That is, the electrostatic force can be attractive or repulsive, depending on the mutual orientation of the molecules. When molecules are in thermal motion, as they are in the gas and liquid phase, the electrostatic force is averaged out to a large extent, because the molecules thermally rotate and thus probe both repulsive and attractive parts of the electrostatic force. Sometimes this effect is expressed by the statement that "random thermal motion around room temperature can usually overcome or disrupt them" (which refers to the electrostatic component of the Van der Waals force). Clearly, the thermal averaging effect is much less pronounced for the attractive induction and dispersion forces.

The Lennard-Jones potential is often used as an approximate model for the isotropic part of a total (repulsion plus attraction) van der Waals force as a function of distance.

Van der Waals forces are responsible for certain cases of pressure broadening (van der Waals broadening) of spectral lines and the formation of van der Waals molecules.

See this URL for an introductory description of the Van der Waals force (as a sum of attractive components only).

London dispersion force

London dispersion forces, named after the German-American physicist Fritz London, are weak intermolecular forces that arise from the attractive force between transient dipoles (or better multipoles) in molecules without permanent multipole moments. London dispersion forces are also known as dispersion forces, London forces, induced dipole-induced dipole forces, or, as van der Waals forces.

London forces can be exhibited by nonpolar molecules because electron density moves about a molecule probabilistically, see quantum mechanical theory of dispersion forces. There is a high chance that the electron density will not be evenly distributed throughout a nonpolar molecule. When an uneven distribution occurs, a temporary multipole is created. This multipole may interact with other nearby multipoles. London forces are also present in polar molecules, but they are usually only a small part of the total interaction force.

Electron density in a molecule may be redistributed by proximity to another multipole. Electrons will gather on the side of a molecule that faces a positive charge and will retreat from a negative charge. Hence, a transient multipole can be produced by a nearby polar molecule, or even by a transient multipole in another nonpolar molecule.

In vacuum, London forces are weaker than other intermolecular forces such as ionic interactions, hydrogen bonding, or permanent dipole-dipole interactions.

This phenomenon is the only attractive intermolecular force at large distances present between neutral atoms (e.g., helium), and is the major attractive force between non-polar molecules, (e.g., nitrogen or methane). Without London forces, there would be no attractive force between noble gas atoms, and they could not then be obtained in a liquid form.

London forces become stronger as the atom (or molecule) in question becomes larger. This is due to the increased polarizability of molecules with larger, more dispersed electron clouds. This trend is exemplified by the halogens (from smallest to largest: F₂, Cl₂, Br₂, I₂). Fluorine and chlorine are gases at room temperature, bromine is a liquid, and iodine is a solid. The London forces also become stronger with larger amounts of surface contact. Greater surface area means closer interaction between different molecules.

Relation to the Casimir effect

The London-van der Waals forces is related to the Casimir effect for dielectric media, the former the microscopic description of the latter bulk property. The first detailed calculations of this were done in 1955 by E. M. Lifshitz.

For further investigation, one may consult the University of St. Andrews' levitation work [1] which relates the Casimir effect to the gecko and how the reversal of the Casimir effect can result in physical levitation of tiny objects.

Use by animals

The ability of geckos to climb on sheer surfaces is attributed to van der Waals force^[1]. A gecko can hang on a glass surface using only one toe. Efforts continue to create a synthetic "gecko tape" that exploits this knowledge. So far, research has produced some promising results - early research yielded an adhesive tape^[2] product, which only obtains a fraction of the forces measured from the natural material, and new research^[3] has yielded a discovery that purports 200 times the adhesive forces of the natural material. Researchers at Rensselaer Polytechnic Institute and the University of Akron announced in a paper published in the June 18–22, 2007 issue of the Proceedings of the National Academy of Sciences that they have created a synthetic “gecko tape” with four times the sticking power of a natural gecko foot^[4].

Researchers at Stanford University and Carnegie Mellon University recently developed a gecko-like robot which uses synthetic setae to climb walls^[5].

See also

• Chemical bond
• Hydride
• John Lennard-Jones
• Lennard-Jones potential
• Ideal gas law
• van der Waals molecule
• Hamaker theory

Sources

• Iver Brevik, V. N. Marachevsky, Kimball A. Milton, Identity of the Van der Waals Force and the Casimir Effect and the Irrelevance of these Phenomena to Sonoluminescence, hep-th/9901011
• I. D. Dzyaloshinskii, E. M. Lifshitz, and L. P. Pitaevskii, Usp. Fiz. Nauk 73, 381 (1961)
• English translation: Soviet Phys. Usp. 4, 153 (1961)
• L. D. Landau and E. M. Lifshitz, Electrodynamics of Continuous Media, Pergamon, Oxford, 1960, pp. 368–376.
• Mark Lefers, "Van der Waals dispersion force". Holmgren Lab.
• E. M. Lifshitz, Zh. Eksp. Teor. Fiz. 29, 894 (1955)
• English translation: Soviet Phys. JETP 2, 73 (1956)
• Western Oregon University's "London force". Intermolecular Forces. (animation)