Jump to content

G-strain

From Wikipedia, the free encyclopedia

This is the current revision of this page, as edited by Herravondure (talk | contribs) at 23:53, 6 May 2022 (Successfully de-orphaned! Wikiproject Orphanage: You can help!). The present address (URL) is a permanent link to this version.

(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)

In EPR spectroscopy, g-strain refers to broadening of g-values owing to small sample inhomogeneity owing to slight variations in the orientation of the paramagnetic centers. The phenomenon is indicated by broadening of the g-values that depends on the frequency of the spectrometer, such as X- or Q-band. If the line width were determined only by hyperfine coupling (which are field-independent), then the line widths would also be field independent, but they often are not. In iron-sulfur proteins, some other metalloproteins, as well as some solids, g-strain can be substantial.[1]

References

[edit]
  1. ^ Wilfred R. Hagen "EPR Spectroscopy of Iron-Sulfur Proteins" Advances in Inorganic Chemistry 1992, vol. 38, p. 165.