# Friedel's law

### From Online Dictionary of Crystallography

##### Revision as of 08:07, 25 March 2006 by AndreAuthier (talk | contribs)

Loi de Friedel (*Fr*). Friedelsche Gesetz (*Ge*). Ley de Friedel (*Sp*).

## Definition

Friedel's law, or rule, states that the intensities of the *h*, *k*, *l* and [math]{\bar h}, {\bar k}, {\bar l}[/math] reflections are equal. This is only true if there is no absorption. It is in that case not possible to tell by diffraction whether an inversion center is present or not. The apparent symmetry of the crystal is then one of the eleven Laue classes.

The reason for Friedel's rule is that the diffracted intensity is proportional to the the square of the modulus of the structure factor, |*F _{h}*|

^{2}, according to the geometrical, or kinematical theory of diffraction. It depends similarly on the modulus of the structure factor according to the dynamical theory of diffraction. The structure factor is given by:

[math]F_h = \Sigma_j f_j {\rm exp - 2 \pi i} {\bold h} . {\bold r_j}[/math]

where *f _{j}* is the atomic scattering factor of atom

*j*,

**h**the reflection vector and [math]{\bold r_j}[/math] the position vector of atom

*j*. There comes:

[math]|F_h|^2 = F_h F_h^* = F_h F_{\bar h} = |F_{\bar h}|^2 [/math]

if the atomic scattering factor, *f _{j}*, is real. The intensities of the

*h*,

*k*,

*l*and [math]{\bar h}, {\bar k}, {\bar l}[/math] reflections are then equal. If the crystal is absorbing, however, due to anomalous dispersion, the atomic scattering factor is complex and

[math]F_{\bar h} \ne F_h^*[/math]

Friedel's law therefore does not hold for absorbing crystals. The reflections *h*, *k*, *l* and [math]{\bar h}, {\bar k}, {\bar l}[/math] are called a Friedel pair. They are used in the resolution of the phase problem for the solution of crystal structures.

## History

Friedel's law was stated by G. Friedel (1865-1933) in 1913 (Friedel G., 1913, *Sur les symétries cristallines que peut révéler la diffraction des rayons X.*, *C.R. Acad. Sci. Paris*, **157**, 1533-1536.

## See also

Absolute structure

Section 3.1 of *International Tables of crystallography, Volume A*