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'''Magnetic dipole–dipole interaction''', also called '''dipolar coupling''', refers to the direct interaction between two [[magnetic dipole]]s. The [[potential energy]] of the interaction is as follows:
 
::<math> H = - \frac{ \mu_0 } {4 \pi r_{jk}^3 } \left( 3 (\bold{m}_j \cdot \bold{e}_{jk})  (\bold{m}_k \cdot \bold{e}_{jk}) - \bold{m}_j \cdot \bold{m}_k \right) </math>
 
where '''e'''<sub>jk</sub> is a unit vector parallel to the line joining the centers of the two dipoles. r<sub>jk</sub> is the distance between two dipoles, '''m'''<sub>k</sub> and '''m'''<sub>j</sub>.
 
For two interacting nuclear [[Spin (physics)|spin]]s
 
::<math> H = - \frac{ \mu_0 }{ 4 \pi } \frac{ \gamma_j \gamma_k \hbar^2}{ r_{jk}^3 } \left( 3 (\bold{I}_j \cdot \bold{e}_{jk})  (\bold{I}_k \cdot \bold{e}_{jk}) - \bold{I}_j \cdot \bold{I}_k \right) </math>
 
where <math>\mu_0</math> is the [[magnetic constant]], <math>\gamma_j</math>, <math>\gamma_k</math> are [[gyromagnetic ratio]]s of two spins, and r<sub>jk</sub> is the distance between the two spins.
 
Force between two magnetic dipoles:
 
: <math>
\vec{F}_{ab}= \frac {3 \mu_0} {4 \pi |r|^4} [ (\hat r \times \vec{m}_a) \times \vec{m}_b + (\hat r \times \vec{m}_b) \times \vec{m}_a - 2 \hat r(\vec{m}_a \cdot \vec{m}_b) + 5 \hat r ((\hat r \times \vec{m}_a) \cdot (\hat r \times \vec{m}_b)) ]
 
</math>
 
where <math>\hat{r}</math> is [[unit vector]] pointing from magnetic moment <math>m_a</math> to <math>m_b</math>, and <math>|r|</math> is the distance between those two magnetic dipole moments.
 
== Dipolar coupling and NMR spectroscopy ==
The direct dipole-dipole coupling is very useful for molecular structural studies, since it depends only on known physical constants and the inverse cube of internuclear distance. Estimation of this coupling provides a direct spectroscopic route to the distance between nuclei and hence the geometrical form of the molecule, or additionally also on intermolecular distances in the solid state leading to [[NMR crystallography]] notably in amorphous materials. Although internuclear magnetic dipole couplings contain a great deal of structural information, in isotropic solution, they average to zero as a result of rotational diffusion. However, their effect on nuclear spin relaxation results in measurable [[nuclear Overhauser effect]]s (NOEs).
 
The [[residual dipolar coupling]] (RDC) occur if the molecules in solution exhibit a partial alignment leading to an incomplete averaging of spatially anisotropic magnetic interactions i.e. dipolar couplings. RDC measurement provides information on the global [[Protein folding|folding]] of the protein-long distance structural information. It also provides information about "slow" dynamics in molecules
 
==References==
*Malcolm H. Levitt, ''Spin Dynamics: Basics of Nuclear Magnetic Resonance''. ISBN 0-471-48922-0.
 
== See also ==
*[[J-coupling]]
*[[Magic angle]]
*[[Residual dipolar coupling]]
*[[Nuclear Overhauser effect]]
*[[Magnetic moment]]
 
{{DEFAULTSORT:Magnetic dipole-dipole interaction}}
[[Category:Electromagnetism]]
[[Category:Nuclear magnetic resonance]]

Revision as of 06:01, 5 August 2013

Magnetic dipole–dipole interaction, also called dipolar coupling, refers to the direct interaction between two magnetic dipoles. The potential energy of the interaction is as follows:

H=μ04πrjk3(3(𝐦j𝐞jk)(𝐦k𝐞jk)𝐦j𝐦k)

where ejk is a unit vector parallel to the line joining the centers of the two dipoles. rjk is the distance between two dipoles, mk and mj.

For two interacting nuclear spins

H=μ04πγjγk2rjk3(3(𝐈j𝐞jk)(𝐈k𝐞jk)𝐈j𝐈k)

where μ0 is the magnetic constant, γj, γk are gyromagnetic ratios of two spins, and rjk is the distance between the two spins.

Force between two magnetic dipoles:

Fab=3μ04π|r|4[(r̂×ma)×mb+(r̂×mb)×ma2r̂(mamb)+5r̂((r̂×ma)(r̂×mb))]

where r̂ is unit vector pointing from magnetic moment ma to mb, and |r| is the distance between those two magnetic dipole moments.

Dipolar coupling and NMR spectroscopy

The direct dipole-dipole coupling is very useful for molecular structural studies, since it depends only on known physical constants and the inverse cube of internuclear distance. Estimation of this coupling provides a direct spectroscopic route to the distance between nuclei and hence the geometrical form of the molecule, or additionally also on intermolecular distances in the solid state leading to NMR crystallography notably in amorphous materials. Although internuclear magnetic dipole couplings contain a great deal of structural information, in isotropic solution, they average to zero as a result of rotational diffusion. However, their effect on nuclear spin relaxation results in measurable nuclear Overhauser effects (NOEs).

The residual dipolar coupling (RDC) occur if the molecules in solution exhibit a partial alignment leading to an incomplete averaging of spatially anisotropic magnetic interactions i.e. dipolar couplings. RDC measurement provides information on the global folding of the protein-long distance structural information. It also provides information about "slow" dynamics in molecules

References

  • Malcolm H. Levitt, Spin Dynamics: Basics of Nuclear Magnetic Resonance. ISBN 0-471-48922-0.

See also