Electric Dipole Moment

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## Elementary definition

## Energy and torque

## Expression (general case)

## Potential and field of an electric dipole

## Dipole moment density and polarization density

### Medium with charge and dipole densities

#### Surface charge

#### Dielectric sphere in uniform external electric field

### General media

## Electric dipole moments of fundamental particles

## Dipole moments of molecules

## See also

## References and in-line notes

## Further reading

## External links

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Electric Dipole Moment

The **electric dipole moment** is a measure of the separation of positive and negative electrical charges within a system, that is, a measure of the system's overall polarity. The SI units for electric dipole moment are coulomb-meter (C?m); however, a commonly used unit in atomic physics and chemistry is the debye (D).

Theoretically, an electric dipole is defined by the first-order term of the multipole expansion; it consists of two equal and opposite charges that are infinitesimally close together, although real dipoles have separated charge.^{[1]} However, when making measurements at a distance much larger than the charge separation, the dipole gives a good approximation of the actual electric field. The dipole is represented by a vector from the negative charge towards the positive charge.

Often in physics the dimensions of a massive object can be ignored and can be treated as a pointlike object, i.e. a point particle. Point particles with electric charge are referred to as point charges. Two point charges, one with charge +*q* and the other one with charge −*q* separated by a distance *d*, constitute an *electric dipole* (a simple case of an electric multipole). For this case, the electric dipole moment has a magnitude

and is directed from the negative charge to the positive one. Some authors may split *d* in half and use *s* = *d*/2 since this quantity is the distance between either charge and the center of the dipole, leading to a factor of two in the definition.

A stronger mathematical definition is to use vector algebra, since a quantity with magnitude and direction, like the dipole moment of two point charges, can be expressed in vector form

where **d** is the displacement vector pointing from the negative charge to the positive charge. The electric dipole moment vector **p** also points from the negative charge to the positive charge.

An idealization of this two-charge system is the electrical point dipole consisting of two (infinite) charges only infinitesimally separated, but with a finite **p**.

This quantity is used in the definition of polarization density.

An object with an electric dipole moment is subject to a torque *τ* when placed in an external electric field. The torque tends to align the dipole with the field. A dipole aligned parallel to an electric field has lower potential energy than a dipole making some angle with it. For a spatially uniform electric field **E**, the energy *U* and the torque are given by^{[2]}

where **p** is the dipole moment, and the symbol "×" refers to the vector cross product. The field vector and the dipole vector define a plane, and the torque is directed normal to that plane with the direction given by the right-hand rule.

A dipole oriented co- or anti-parallel to the direction in which a non-uniform electric field is increasing (gradient of the field) will experience a torque, as well as a force in the direction of its dipole moment. It can be shown that this force will always be parallel to the dipole moment regardless of co- or anti-parallel orientation of the dipole.

More generally, for a continuous distribution of charge confined to a volume *V*, the corresponding expression for the dipole moment is:

where **r** locates the point of observation and *d*^{3}**r**_{0} denotes an elementary volume in *V*. For an array of point charges, the charge density becomes a sum of Dirac delta functions:

where each **r**_{i} is a vector from some reference point to the charge *q _{i}*. Substitution into the above integration formula provides:

This expression is equivalent to the previous expression in the case of charge neutrality and *N* = 2. For two opposite charges, denoting the location of the positive charge of the pair as **r**_{+} and the location of the negative charge as **r**_{−} :

showing that the dipole moment vector is directed from the negative charge to the positive charge because the position vector of a point is directed outward from the origin to that point.

The dipole moment is particularly useful in the context of an overall neutral system of charges, for example a pair of opposite charges, or a neutral conductor in a uniform electric field. For such a system of charges, visualized as an array of paired opposite charges, the relation for electric dipole moment is:

where **r** is the point of observation, and **d**_{i} = **r**_{i} - **r**_{i}, **r**_{i} being the position of the negative charge in the dipole *i*, and **r**_{i} the position of the positive charge.
This is the vector sum of the individual dipole moments of the neutral charge pairs. (Because of overall charge neutrality, the dipole moment is independent of the observer's position **r**.) Thus, the value of **p** is independent of the choice of reference point, provided the overall charge of the system is zero.

When discussing the dipole moment of a non-neutral system, such as the dipole moment of the proton, a dependence on the choice of reference point arises. In such cases it is conventional to choose the reference point to be the center of mass of the system, not some arbitrary origin.^{[3]} This choice is not only a matter of convention: the notion of dipole moment is essentially derived from the mechanical notion of torque, and as in mechanics, it is computationally and theoretically useful to choose the center of mass as the observation point. For a charged molecule the center of charge should be the reference point instead of the center of mass. For neutral systems the references point is not important. The dipole moment is an intrinsic property of the system.

An ideal dipole consists of two opposite charges with infinitesimal separation. We compute the potential and field of such an ideal dipole starting with two opposite charges at separation *d >* 0, and taking the limit as *d ->* 0.

Two closely spaced opposite charges ±*q* have a potential of the form:

where the charge separation is:

Let **R** denote the position vector relative to the midpoint **r**, and the corresponding unit vector:

Taylor expansion in (see multipole expansion and quadrupole) expresses this potential as a series.^{[4]}^{[5]}

where higher order terms in the series are vanishing at large distances, *R*, compared to *d*.^{[6]} Here, the electric dipole moment **p** is, as above:

The result for the dipole potential also can be expressed as:^{[7]}

which relates the dipole potential to that of a point charge. A key point is that the potential of the dipole falls off faster with distance *R* than that of the point charge.

The electric field of the dipole is the negative gradient of the potential, leading to:^{[7]}

Thus, although two closely spaced opposite charges are *not quite* an ideal electric dipole (because their potential at short distances is not that of a dipole), at distances much larger than their separation, their dipole moment **p** appears directly in their potential and field.

As the two charges are brought closer together (*d* is made smaller), the dipole term in the multipole expansion based on the ratio *d*/*R* becomes the only significant term at ever closer distances *R*, and in the limit of infinitesimal separation the dipole term in this expansion is all that matters. As *d* is made infinitesimal, however, the dipole charge must be made to increase to hold **p** constant. This limiting process results in a "point dipole".

The dipole moment of an array of charges,

determines the degree of polarity of the array, but for a neutral array it is simply a vector property of the array with no information about the array's absolute location. The dipole moment *density* of the array **p**(**r**) contains both the location of the array and its dipole moment. When it comes time to calculate the electric field in some region containing the array, Maxwell's equations are solved, and the information about the charge array is contained in the *polarization density* **P**(**r**) of Maxwell's equations. Depending upon how fine-grained an assessment of the electric field is required, more or less information about the charge array will have to be expressed by **P**(**r**). As explained below, sometimes it is sufficiently accurate to take **P**(**r**) = **p**(**r**). Sometimes a more detailed description is needed (for example, supplementing the dipole moment density with an additional quadrupole density) and sometimes even more elaborate versions of **P**(**r**) are necessary.

It now is explored just in what way the polarization density **P**(**r**) that enters Maxwell's equations is related to the dipole moment **p** of an overall neutral array of charges, and also to the *dipole moment density* **p**(**r**) (which describes not only the dipole moment, but also the array location). Only static situations are considered in what follows, so **P(r)** has no time dependence, and there is no displacement current. First is some discussion of the polarization density **P**(**r**). That discussion is followed with several particular examples.

A formulation of Maxwell's equations based upon division of charges and currents into "free" and "bound" charges and currents leads to introduction of the **D**- and **P**-fields:

where **P** is called the polarization density. In this formulation, the divergence of this equation yields:

and as the divergence term in **E** is the *total* charge, and *? _{f}* is "free charge", we are left with the relation:

with *? _{b}* as the bound charge, by which is meant the difference between the total and the free charge densities.

As an aside, in the absence of magnetic effects, Maxwell's equations specify that

which implies

Applying Helmholtz decomposition:^{[8]}

for some scalar potential *?*, and:

Suppose the charges are divided into free and bound, and the potential is divided into

Satisfaction of the boundary conditions upon *?* may be divided arbitrarily between *? _{f}* and

Next is discussed how several different dipole moment descriptions of a medium relate to the polarization entering Maxwell's equations.

As described next, a model for polarization moment density **p**(**r**) results in a polarization

restricted to the same model. For a smoothly varying dipole moment distribution **p**(**r**), the corresponding bound charge density is simply

as we will establish shortly via integration by parts. However, if **p**(**r**) exhibits an abrupt step in dipole moment at a boundary between two regions, ?·**p**(**r**) results in a surface charge component of bound charge. This surface charge can be treated through a surface integral, or by using discontinuity conditions at the boundary, as illustrated in the various examples below.

As a first example relating dipole moment to polarization, consider a medium made up of a continuous charge density *?*(**r**) and a continuous dipole moment distribution **p**(**r**).^{[11]} The potential at a position **r** is:^{[12]}^{[13]}

where *?*(**r**) is the unpaired charge density, and **p**(**r**) is the dipole moment density.^{[14]} Using an identity:

the polarization integral can be transformed:

The first term can be transformed to an integral over the surface bounding the volume of integration, and contributes a surface charge density, discussed later. Putting this result back into the potential, and ignoring the surface charge for now:

where the volume integration extends only up to the bounding surface, and does not include this surface.

The potential is determined by the total charge, which the above shows consists of:

showing that:

In short, the dipole moment density **p**(**r**) plays the role of the polarization density **P** for this medium. Notice, **p**(**r**) has a non-zero divergence equal to the bound charge density (as modeled in this approximation).

It may be noted that this approach can be extended to include all the multipoles: dipole, quadrupole, etc.^{[15]}^{[16]} Using the relation:

the polarization density is found to be:

where the added terms are meant to indicate contributions from higher multipoles. Evidently, inclusion of higher multipoles signifies that the polarization density **P** no longer is determined by a dipole moment density **p** alone. For example, in considering scattering from a charge array, different multipoles scatter an electromagnetic wave differently and independently, requiring a representation of the charges that goes beyond the dipole approximation.^{[17]}

Above, discussion was deferred for the first term in the expression for the potential due to the dipoles. Integrating the divergence results in a surface charge. The figure at the right provides an intuitive idea of why a surface charge arises. The figure shows a uniform array of identical dipoles between two surfaces. Internally, the heads and tails of dipoles are adjacent and cancel. At the bounding surfaces, however, no cancellation occurs. Instead, on one surface the dipole heads create a positive surface charge, while at the opposite surface the dipole tails create a negative surface charge. These two opposite surface charges create a net electric field in a direction opposite to the direction of the dipoles.

This idea is given mathematical form using the potential expression above. Ignoring the free charge, the potential is:

Using the divergence theorem, the divergence term transforms into the surface integral:

with d**A**_{0} an element of surface area of the volume. In the event that **p**(**r**) is a constant, only the surface term survives:

with d**A**_{0} an elementary area of the surface bounding the charges. In words, the potential due to a constant **p** inside the surface is equivalent to that of a *surface charge*

which is positive for surface elements with a component in the direction of **p** and negative for surface elements pointed oppositely. (Usually the direction of a surface element is taken to be that of the outward normal to the surface at the location of the element.)

If the bounding surface is a sphere, and the point of observation is at the center of this sphere, the integration over the surface of the sphere is zero: the positive and negative surface charge contributions to the potential cancel. If the point of observation is off-center, however, a net potential can result (depending upon the situation) because the positive and negative charges are at different distances from the point of observation.^{[18]} The field due to the surface charge is:

which, at the center of a spherical bounding surface is not zero (the *fields* of negative and positive charges on opposite sides of the center add because both fields point the same way) but is instead:^{[19]}

If we suppose the polarization of the dipoles was induced by an external field, the polarization field opposes the applied field and sometimes is called a *depolarization field*.^{[20]}^{[21]} In the case when the polarization is *outside* a spherical cavity, the field in the cavity due to the surrounding dipoles is in the *same* direction as the polarization.^{[22]}

In particular, if the electric susceptibility is introduced through the approximation:

where * E*, in this case and in the following, represent the

Then:

Whenever *?*(**r**) is used to model a step discontinuity at the boundary between two regions, the step produces a surface charge layer. For example, integrating along a normal to the bounding surface from a point just interior to one surface to another point just exterior:

where *A*_{n}, *?*_{n} indicate the area and volume of an elementary region straddling the boundary between the regions, and a unit normal to the surface. The right side vanishes as the volume shrinks, inasmuch as ?_{b} is finite, indicating a discontinuity in * E*, and therefore a surface charge. That is, where the modeled medium includes a step in permittivity, the polarization density corresponding to the dipole moment density

necessarily includes the contribution of a surface charge.^{[23]}^{[24]}^{[25]}

A physically more realistic modeling of **p**(**r**) would have the dipole moment density drop off rapidly, but smoothly to zero at the boundary of the confining region, rather than making a sudden step to zero density. Then the surface charge will not concentrate in an infinitely thin surface, but instead, being the divergence of a smoothly varying dipole moment density, will distribute itself throughout a thin, but finite transition layer.

The above general remarks about surface charge are made more concrete by considering the example of a dielectric sphere in a uniform electric field.^{[27]}^{[28]} The sphere is found to adopt a surface charge related to the dipole moment of its interior.

A uniform external electric field is supposed to point in the *z*-direction, and spherical-polar coordinates are introduced so the potential created by this field is:

The sphere is assumed to be described by a dielectric constant *?*, that is,

and inside the sphere the potential satisfies Laplace's equation. Skipping a few details, the solution inside the sphere is:

while outside the sphere:

At large distances, ?_{>} -> ?_{? } so *B* = -*E _{? }*. Continuity of potential and of the radial component of displacement

As a consequence, the potential is:

which is the potential due to applied field and, in addition, a dipole in the direction of the applied field (the *z*-direction) of dipole moment:

or, per unit volume:

The factor (*?* - 1)/(*?* + 2) is called the Clausius-Mossotti factor and shows that the induced polarization flips sign if *?* < 1. Of course, this cannot happen in this example, but in an example with two different dielectrics *?* is replaced by the ratio of the inner to outer region dielectric constants, which can be greater or smaller than one. The potential inside the sphere is:

leading to the field inside the sphere:

showing the depolarizing effect of the dipole. Notice that the field inside the sphere is *uniform* and parallel to the applied field. The dipole moment is uniform throughout the interior of the sphere. The surface charge density on the sphere is the difference between the radial field components:

This linear dielectric example shows that the dielectric constant treatment is equivalent to the uniform dipole moment model and leads to zero charge everywhere except for the surface charge at the boundary of the sphere.

If observation is confined to regions sufficiently remote from a system of charges, a multipole expansion of the exact polarization density can be made. By truncating this expansion (for example, retaining only the dipole terms, or only the dipole and quadrupole terms, or *etc.*), the results of the previous section are regained. In particular, truncating the expansion at the dipole term, the result is indistinguishable from the polarization density generated by a uniform dipole moment confined to the charge region. To the accuracy of this dipole approximation, as shown in the previous section, the dipole moment *density* **p**(**r**) (which includes not only **p** but the location of **p**) serves as **P**(**r**).

At locations *inside* the charge array, to connect an array of paired charges to an approximation involving only a dipole moment density **p**(**r**) requires additional considerations. The simplest approximation is to replace the charge array with a model of ideal (infinitesimally spaced) dipoles. In particular, as in the example above that uses a constant dipole moment density confined to a finite region, a surface charge and depolarization field results. A more general version of this model (which allows the polarization to vary with position) is the customary approach using electric susceptibility or electrical permittivity.

A more complex model of the point charge array introduces an effective medium by averaging the microscopic charges;^{[21]} for example, the averaging can arrange that only dipole fields play a role.^{[29]}^{[30]} A related approach is to divide the charges into those nearby the point of observation, and those far enough away to allow a multipole expansion. The nearby charges then give rise to *local field effects*.^{[19]}^{[31]} In a common model of this type, the distant charges are treated as a homogeneous medium using a dielectric constant, and the nearby charges are treated only in a dipole approximation.^{[32]} The approximation of a medium or an array of charges by only dipoles and their associated dipole moment density is sometimes called the *point dipole* approximation, the *discrete dipole approximation*, or simply the *dipole approximation*.^{[33]}^{[34]}^{[35]}

Not to be confused with spin which refers to the magnetic dipole moments of particles, much experimental work is continuing on measuring the electric dipole moments (EDM) of fundamental and composite particles, namely those of the electron and neutron, respectively. As EDMs violate both the parity (P) and time-reversal (T) symmetries, their values yield a mostly model-independent measure of CP-violation in nature (assuming CPT symmetry is valid).^{[36]} Therefore, values for these EDMs place strong constraints upon the scale of CP-violation that extensions to the standard model of particle physics may allow. Current generations of experiments are designed to be sensitive to the supersymmetry range of EDMs, providing complementary experiments to those done at the LHC.^{[37]}

Indeed, many theories are inconsistent with the current limits and have effectively been ruled out, and established theory permits a much larger value than these limits, leading to the strong CP problem and prompting searches for new particles such as the axion.^{[38]}

Dipole moments in molecules are responsible for the behavior of a substance in the presence of external electric fields. The dipoles tend to be aligned to the external field which can be constant or time-dependent. This effect forms the basis of a modern experimental technique called dielectric spectroscopy.

Dipole moments can be found in common molecules such as water and also in biomolecules such as proteins.^{[39]}

By means of the total dipole moment of some material one can compute the dielectric constant which is related to the more intuitive concept of conductivity. If is the total dipole moment of the sample, then the dielectric constant is given by,

where *k* is a constant and is the time correlation function of the total dipole moment. In general the total dipole moment have contributions coming
from translations and rotations of the molecules in the sample,

Therefore, the dielectric constant (and the conductivity) has contributions from both terms. This approach can be generalized to compute the frequency dependent dielectric function.^{[40]}

It is possible to calculate dipole moments from electronic structure theory, either as a response to constant electric fields or from the density matrix.^{[41]} Such values however are not directly comparable to experiment due to the potential presence of nuclear quantum effects, which can be substantial for even simple systems like the ammonia molecule.^{[42]}Coupled cluster theory (especially CCSD(T)^{[43]}) can give very accurate dipole moments,^{[44]} although it is possible to get reasonable estimates (within about 5%) from density functional theory, especially if hybrid or double hybrid functionals are employed.^{[45]} The dipole moment of a molecule can also be calculated based on the molecular structure using the concept of group contribution methods.^{[46]}

**^**Many theorists predict elementary particles can have very tiny electric dipole moments, possibly without separated charge. Such large dipoles make no difference to everyday physics, and have not yet been observed. (See electron electric dipole moment).**^**Raymond A. Serway; John W. Jewett Jr. (2009).*Physics for Scientists and Engineers, Volume 2*(8th ed.). Cengage Learning. p. 756-757. ISBN 978-1439048399.**^**Christopher J. Cramer (2004).*Essentials of computational chemistry*(2nd ed.). Wiley. p. 307. ISBN 978-0-470-09182-1.**^**David E Dugdale (1993).*Essentials of Electromagnetism*. Springer. pp. 80-81. ISBN 978-1-56396-253-0.**^**Kikuji Hirose; Tomoya Ono; Yoshitaka Fujimoto (2005).*First-principles calculations in real-space formalism*. Imperial College Press. p. 18. ISBN 978-1-86094-512-0.**^**Each succeeding term provides a more detailed view of the distribution of charge, and falls off more rapidly with distance. For example, the*quadrupole moment*is the basis for the next term:**r**= (x_{0}_{1}, x_{2}, x_{3}). See HW Wyld (1999).*Mathematical Methods for Physics*. Westview Press. p. 106. ISBN 978-0-7382-0125-2.- ^
^{a}^{b}BB Laud (1987).*Electromagnetics*(2nd ed.). New Age International. p. 25. ISBN 978-0-85226-499-7. **^**Jie-Zhi Wu; Hui-Yang Ma; Ming-De Zhou (2006). "§2.3.1 Functionally Orthogonal Decomposition".*Vorticity and vortex dynamics*. Springer. pp. 36*ff*. ISBN 978-3-540-29027-8.**^**For example, one could place the boundary around the bound charges at infinity. Then*?*falls off with distance from the bound charges. If an external field is present, and zero free charge, the field can be accounted for in the contribution of_{b}*?*, which would arrange to satisfy the boundary conditions and Laplace's equation_{f}**^**In principle, one could add the same arbitrary*curl*to both**D**and**P**, which would cancel out of the difference**D**-**P**. However, assuming**D**and**P**originate in a simple division of charges into free and bound, they a formally similar to electric fields and so have zero*curl*.**^**This medium can be seen as an idealization growing from the multipole expansion of the potential of an arbitrarily complex charge distribution, truncation of the expansion, and the forcing of the truncated form to apply everywhere. The result is a hypothetical medium. See Jack Vanderlinde (2004). "§7.1 The electric field due to a polarized dielectric".*Classical Electromagnetic Theory*. Springer. ISBN 978-1-4020-2699-7.**^**Uwe Krey; Anthony Owen (2007).*Basic Theoretical Physics: A Concise Overview*. Springer. pp. 138-143. ISBN 978-3-540-36804-5.**^**T Tsang (1997).*Classical Electrodynamics*. World Scientific. p. 59. ISBN 978-981-02-3041-8.**^**For example, for a system of ideal dipoles with dipole moment**p**confined within some closed surface, the*dipole density***p**(**r**) is equal to**p**inside the surface, but is zero outside. That is, the dipole density includes a Heaviside step function locating the dipoles inside the surface.**^**George E Owen (2003).*Introduction to Electromagnetic Theory*(republication of the 1963 Allyn & Bacon ed.). Courier Dover Publications. p. 80. ISBN 978-0-486-42830-7.**^**Pierre-François Brevet (1997).*Surface second harmonic generation*. Presses polytechniques et universitaires romandes. p. 24. ISBN 978-2-88074-345-1.**^**See Daniel A. Jelski; Thomas F. George (1999).*Computational studies of new materials*. World Scientific. p. 219. ISBN 978-981-02-3325-9. and EM Purcell; CR Pennypacker (1973). "Scattering and Absorption of Light by Nonspherical Dielectric Grains".*Astrophysical Journal*.**186**: 705-714. Bibcode:1973ApJ...186..705P. doi:10.1086/152538.**^**A brute force evaluation of the integral can be done using a multipole expansion: . See HW Wyld (1999).*Mathematical Methods for Physics*. Westview Press. p. 104. ISBN 978-0-7382-0125-2.- ^
^{a}^{b}H. Ibach; Hans Lüth (2003).*Solid-state Physics: an introduction to principles of materials science*(3rd ed.). Springer. p. 361. ISBN 978-3-540-43870-0. **^**Yasuaki Masumoto; Toshihide Takagahara (2002).*Semiconductor quantum dots: physics, spectroscopy, and applications*. Springer. p. 72. ISBN 978-3-540-42805-3.- ^
^{a}^{b}Yutaka Toyozawa (2003).*Optical processes in solids*. Cambridge University Press. p. 96. ISBN 978-0-521-55605-7. **^**For example, a droplet in a surrounding medium experiences a higher or a lower internal field depending upon whether the medium has a higher or a lower dielectric constant than that of the droplet. See Paul S. Drzaic (1995).*Liquid crystal dispersions*. World Scientific. p. 246. ISBN 978-981-02-1745-7.**^**Wai-Kai Chen (2005).*The electrical engineering handbook*. Academic Press. p. 502. ISBN 978-0-12-170960-0.**^**Julius Adams Stratton (2007).*Electromagnetic theory*(reprint of 1941 ed.). Wiley-IEEE. p. 184. ISBN 978-0-470-13153-4.**^**Edward J. Rothwell; Michael J. Cloud (2001).*Electromagnetics*. CRC Press. p. 68. ISBN 978-0-8493-1397-4.**^**Based upon equations from Andrew Gray (1888).*The theory and practice of absolute measurements in electricity and magnetism*. Macmillan & Co. pp. 126-127., which refers to papers by Sir W. Thomson.**^**HW Wyld (1999).*Mathematical Methods for Physics*(2nd ed.). Westview Press. pp. 233*ff*. ISBN 978-0-7382-0125-2.**^**Julius Adams Stratton (2007).*Electromagnetic theory*(Wiley-IEEE reissue ed.). Piscataway, NJ: IEEE Press. p. 205*ff*. ISBN 978-0-470-13153-4.**^**John E Swipe; RW Boyd (2002). "Nanocomposite materials for nonlinear optics based upon local field effects". In Vladimir M. Shalaev (ed.).*Optical properties of nanostructured random media*. Springer. p. 3. ISBN 978-3-540-42031-6.**^**Emil Wolf (1977).*Progress in Optics*. Elsevier. p. 288. ISBN 978-0-7204-1515-5.**^**Mark Fox (2006).*Optical Properties of Solids*. Oxford University Press. p. 39. ISBN 978-0-19-850612-6.**^**Lev Kantorovich (2004). "§8.2.1 The local field".*Quantum theory of the solid state*. Springer. p. 426. ISBN 978-1-4020-2153-4.**^**Pierre Meystre (2001).*Atom Optics*. Springer. p. 5. ISBN 978-0-387-95274-1.**^**Bruce T Draine (2001). "The discrete dipole approximation for light scattering by irregular targets". In Michael I. Mishchenko (ed.).*Light scattering by nonspherical particles*. Academic Press. p. 132. ISBN 978-0-12-498660-2.**^**MA Yurkin; AG Hoekstra (2007). "The discrete dipole approximation: an overview and recent developments".*Journal of Quantitative Spectroscopy and Radiative Transfer*.**106**(1-3): 558-589. arXiv:0704.0038. Bibcode:2007JQSRT.106..558Y. doi:10.1016/j.jqsrt.2007.01.034. S2CID 119572857.**^**Khriplovich, Iosip B.; Lamoreaux, Steve K. (2012).*CP violation without strangeness : electric dipole moments of particles, atoms, and molecules*. [S.l.]: Springer. ISBN 978-3-642-64577-8.**^**Ibrahim, Tarik; Itani, Ahmad; Nath, Pran (2014). "Electron EDM as a Sensitive Probe of PeV Scale Physics".*Physical Review D*.**90**(5): 055006. arXiv:1406.0083. Bibcode:2014PhRvD..90e5006I. doi:10.1103/PhysRevD.90.055006. S2CID 118880896.**^**Kim, Jihn E.; Carosi, Gianpaolo (2010). "Axions and the strong CP problem".*Reviews of Modern Physics*.**82**(1): 557-602. arXiv:0807.3125. Bibcode:2010RvMP...82..557K. doi:10.1103/RevModPhys.82.557.**^**Ojeda, P.; Garcia, M. (2010). "Electric Field-Driven Disruption of a Native beta-Sheet Protein Conformation and Generation of a Helix-Structure".*Biophysical Journal*.**99**(2): 595-599. Bibcode:2010BpJ....99..595O. doi:10.1016/j.bpj.2010.04.040. PMC 2905109. PMID 20643079.**^**Y. Shim; H. Kim (2008). "Dielectric Relaxation, Ion Conductivity, Solvent Rotation, and Solvation Dynamics in a Room-Temperature Ionic Liquid".*J. Phys. Chem. B*.**112**(35): 11028-11038. doi:10.1021/jp802595r. PMID 18693693.**^**Frank., Jensen (2007).*Introduction to computational chemistry*(2nd ed.). Chichester, England: John Wiley & Sons. ISBN 9780470011874. OCLC 70707839.**^**Puzzarini, Cristina (2008-09-01). "Ab initio characterization of XH3 (X = N,P). Part II. Electric, magnetic and spectroscopic properties of ammonia and phosphine".*Theoretical Chemistry Accounts*.**121**(1-2): 1-10. doi:10.1007/s00214-008-0409-8. ISSN 1432-881X. S2CID 98782005.**^**Raghavachari, Krishnan; Trucks, Gary W.; Pople, John A.; Head-Gordon, Martin (1989). "A fifth-order perturbation comparison of electron correlation theories".*Chemical Physics Letters*.**157**(6): 479-483. Bibcode:1989CPL...157..479R. doi:10.1016/s0009-2614(89)87395-6.**^**Helgaker, Trygve; Jørgensen, Poul; Olsen, Jeppe (2000).*Molecular electronic-structure theory*(Submitted manuscript). Wiley. doi:10.1002/9781119019572. ISBN 9781119019572.**^**Hait, Diptarka; Head-Gordon, Martin (2018-03-21). "How Accurate Is Density Functional Theory at Predicting Dipole Moments? An Assessment Using a New Database of 200 Benchmark Values".*Journal of Chemical Theory and Computation*.**14**(4): 1969-1981. arXiv:1709.05075. doi:10.1021/acs.jctc.7b01252. PMID 29562129. S2CID 4391272.**^**K. Müller; L. Mokrushina; W. Arlt (2012). "Second-Order Group Contribution Method for the Determination of the Dipole Moment".*J. Chem. Eng. Data*.**57**(4): 1231-1236. doi:10.1021/je2013395.

- Melvin Schwartz (1987). "Electrical DIPOLE MOMENT".
*Principles of Electrodynamics*(reprint of 1972 ed.). Courier Dover Publications. p. 49*ff*. ISBN 978-0-486-65493-5.

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