International Tables for Crystallography (2006). Vol. C. ch. 6.1, pp. 554-595
https://doi.org/10.1107/97809553602060000600 |
Chapter 6.1. Intensity of diffracted intensities
Chapter index
Anharmonicity 6.1.1.6
Associated Legendre polynomials 6.1.1.4
Born approximation 6.1.2.2
Bragg reflection
magnetic 6.1.2.3
Coherent (Rayleigh) scattering 6.1.1.1
Collinear structures 6.1.2.3
Compton scattering 6.1.1.2
Crystal(s)
reflecting power 6.1.1.8
Cumulant expansion 6.1.1.6.3
Flipping ratios 6.1.2.5
Fourier-invariant expansions 6.1.1.6.2
Gram–Charlier series expansion 6.1.1.6.1
Hermite polynomial tensors 6.1.1.6.1
Hydrogen-atom scattering factors 6.1.1.2
Intensity
of diffracted intensities 6.1.1
Kinematic theory 6.1.1.8
Libration (rotational oscillation) 6.1.1.6.5
Magnetic
Bragg reflection 6.1.2.3
form factors 6.1.2.4
interaction vector 6.1.2.2
space group 6.1.2.3
Magnetization density 6.1.2.2
Multipole functions, angle dependence 6.1.1.6
Neutron polarization 6.1.2.6
Orbitals, Slater-type 6.1.1.4
Quasi-Gaussian approximation 6.1.1.6.6
Rayleigh scattering 6.1.1.1
Reflecting power of a crystal 6.1.1.8
Rotational oscillation (libration) 6.1.1.6.5
Rotation of polarization 6.1.2.6
Scattering amplitudes
nuclear 6.1.3.2
Scattering
Compton 6.1.1.2
neutrons, magnetic 6.1.2.2
neutrons, nuclear 6.1.3
Rayleigh 6.1.1.1
spin-flip 6.1.2.2
Scattering lengths
Skewness 6.1.1.6.1
Slater-type orbitals 6.1.1.4
Space groups
magnetic 6.1.2.3
Spin-flip scattering 6.1.2.2
Time reversal 6.1.2.3
Unit cell
magnetic structure factor 6.1.2.3
Vanadium, scattering from 6.1.3.3
X-ray scattering 6.1.1