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In physics, there are several kinds of dipole:
Dipoles can be characterized by their dipole moment, a vector quantity. For the simple electric dipole given above, the electric dipole moment points from the negative charge towards the positive charge, and has a magnitude equal to the strength of each charge times the separation between the charges. (To be precise: for the definition of the dipole moment, one should always consider the "dipole limit", where e.g. the distance of the generating charges should converge to 0, while simultaneously the charge strength should diverge to infinity in such a way that the product remains a positive constant.)
In addition to current loops, the electron, among other fundamental particles, has a magnetic dipole moment. This is because it generates a magnetic field that is identical to that generated by a very small current loop. However, to the best of our[who?] knowledge, the electron's magnetic moment is not due to a current loop, but is instead an intrinsic property of the electron. It is also possible that the electron has an electric dipole moment, although this has not yet been observed (see electron electric dipole moment for more information).
A permanent magnet, such as a bar magnet, owes its magnetism to the intrinsic magnetic dipole moment of the electron. The two ends of a bar magnet are referred to as poles (not to be confused with monopoles), and are labeled "north" and "south". The dipole moment of the bar magnet points from its magnetic south to its magnetic north pole. The north pole of a bar magnet in a compass points north. However, this means that Earth's geomagnetic north pole is the south pole of its dipole moment, and vice versa.
A physical dipole consists of two equal and opposite point charges: in the literal sense, two poles. Its field at large distances (i.e., distances large in comparison to the separation of the poles) depends almost entirely on the dipole moment as defined above. A point (electric) dipole is the limit obtained by letting the separation tend to 0 while keeping the dipole moment fixed. The field of a point dipole has a particularly simple form, and the order-1 term in the multipole expansion is precisely the point dipole field.
Although there are no known magnetic monopoles in nature, there are magnetic dipoles in the form of the quantum-mechanical spin associated with particles such as electrons (although the accurate description of such effects falls outside of classical electromagnetism). A theoretical magnetic point dipole has a magnetic field of exactly the same form as the electric field of an electric point dipole. A very small current-carrying loop is approximately a magnetic point dipole; the magnetic dipole moment of such a loop is the product of the current flowing in the loop and the (vector) area of the loop.
Any configuration of charges or currents has a 'dipole moment', which describes the dipole whose field is the best approximation, at large distances, to that of the given configuration. This is simply one term in the multipole expansion when the total charge ("monopole moment") is 0 — as it always is for the magnetic case, since there are no magnetic monopoles. The dipole term is the dominant one at large distances: Its field falls off in proportion to 1/r3, as compared to 1/r4 for the next (quadrupole) term and higher powers of 1/r for higher terms, or 1/r2 for the monopole term.
Many molecules have such dipole moments due to non-uniform distributions of positive and negative charges on the various atoms. Such is the case with polar compounds like hydrogen fluoride (HF), where electron density is shared unequally between atoms. Therefore, a molecule's dipole is an electric dipole with an inherent electric field which should not be confused with a magnetic dipole which generates a magnetic field.
For molecules there are three types of dipoles:
More generally, an induced dipole of any polarizable charge distribution ρ (remember that a molecule has a charge distribution) is caused by an electric field external to ρ. This field may, for instance, originate from an ion or polar molecule in the vicinity of ρ or may be macroscopic (e.g., a molecule between the plates of a charged capacitor). The size of the induced dipole is equal to the product of the strength of the external field and the dipole polarizability of ρ.
KBr has one of the highest dipole moments because it is a very ionic molecule (which only exists as a molecule in the gas phase).
The overall dipole moment of a molecule may be approximated as a vector sum of bond dipole moments. As a vector sum it depends on the relative orientation of the bonds, so that from the dipole moment information can be deduced about the molecular geometry. For example the zero dipole of CO2 implies that the two C=O bond dipole moments cancel so that the molecule must be linear. For H2O the O-H bond moments do not cancel because the molecule is bent. For ozone (O3) which is also a bent molecule, the bond dipole moments are not zero even though the O-O bonds are between similar atoms. This agrees with the Lewis structures for the resonance forms of ozone which show a positive charge on the central oxygen atom.
An example in organic chemistry of the role of geometry in determining dipole moment is the cis and trans isomers of 1,2-dichloroethene. In the cis isomer the two polar C-Cl bonds are on the same side of the C=C double bond and the molecular dipole moment is 1.90 D. In the trans isomer, the dipole moment is zero because the two C-Cl bond are on opposite sides of the C=C and cancel (and the two bond moments for the much less polar C-H bonds also cancel).
Note that it is critical to verify the geometry of a molecular species before engaging in any calculations of dipole moment. The polarity of individual bonds in a molecule is no guarantee that the molecule is polar. For example, one might readily assume that boron trifluoride is a polar molecule because the difference in electronegativity is greater than the traditionally cited threshold of 1.7. However, due to the equilateral triangular distribution of the fluoride ions about the boron cation center, the molecule as a whole does not exhibit any identifiable pole: one cannot construct a plane that divides the molecule into a net negative part and a net positive part.
Consider a collection of N particles with charges qi and position vectors ri. For instance, this collection may be a molecule consisting of electrons, all with charge −e, and nuclei with charge eZi, where Zi is the atomic number of the i th nucleus. The physical quantity (observable) dipole has the quantum mechanical dipole operator:
A non-degenerate (S-state) atom can have only a zero permanent dipole. This fact follows quantum mechanically from the inversion symmetry of atoms. All 3 components of the dipole operator are antisymmetric under inversion with respect to the nucleus,
where is the dipole operator and is the inversion operator. The permanent dipole moment of an atom in a non-degenerate state (see degenerate energy level) is given as the expectation (average) value of the dipole operator,
where is an S-state, non-degenerate, wavefunction, which is symmetric or antisymmetric under inversion: . Since the product of the wavefunction (in the ket) and its complex conjugate (in the bra) is always symmetric under inversion and its inverse,
it follows that the expectation value changes sign under inversion. We used here the fact that , being a symmetry operator, is unitary: and by definition the Hermitian adjoint may be moved from bra to ket and then becomes . Since the only quantity that is equal to minus itself is the zero, the expectation value vanishes,
In the case of open-shell atoms with degenerate energy levels, one could define a dipole moment by the aid of the first-order Stark effect. This gives a non-vanishing dipole (by definition proportional to a non-vanishing first-order Stark shift) only if some of the wavefunctions belonging to the degenerate energies have opposite parity; i.e., have different behavior under inversion. This is a rare occurrence, but happens for the excited H-atom, where 2s and 2p states are "accidentally" degenerate (see article Laplace–Runge–Lenz vector for the origin of this degeneracy) and have opposite parity (2s is even and 2p is odd).
The far-field strength, B, of a dipole magnetic field is given by
Conversion to cylindrical coordinates is achieved using r2 = z2 + ρ2 and
where ρ is the perpendicular distance from the z-axis. Then,
The field itself is a vector quantity:
This is exactly the field of a point dipole, exactly the dipole term in the multipole expansion of an arbitrary field, and approximately the field of any dipole-like configuration at large distances.
The vector potential A of a magnetic dipole is
with the same definitions as above.
The electrostatic potential at position r due to an electric dipole at the origin is given by:
This term appears as the second term in the multipole expansion of an arbitrary electrostatic potential Φ(r). If the source of Φ(r) is a dipole, as it is assumed here, this term is the only non-vanishing term in the multipole expansion of Φ(r). The electric field from a dipole can be found from the gradient of this potential:
Since the direction of an electric field is defined as the direction of the force on a positive charge, electric field lines point away from a positive charge and toward a negative charge.
for an electric dipole moment p (in coulomb-meters), or
for a magnetic dipole moment m (in ampere-square meters).
The resulting torque will tend to align the dipole with the applied field, which in the case of an electric dipole, yields a potential energy of
The energy of a magnetic dipole is similarly
In addition to dipoles in electrostatics, it is also common to consider an electric or magnetic dipole that is oscillating in time.
In particular, a harmonically oscillating electric dipole is described by a dipole moment of the form
where ω is the angular frequency. In vacuum, this produces fields:
Far away (for ), the fields approach the limiting form of a radiating spherical wave:
which produces a total time-average radiated power P given by
This power is not distributed isotropically, but is rather concentrated around the directions lying perpendicular to the dipole moment. Usually such equations are described by spherical harmonics, but they look very different. A circular polarized dipole is described as a superposition of two linear dipoles.