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Updated: Jun 8, 2026

Rapid Scan Electron Paramagnetic Resonance Opens New Avenues for Imaging Physiologically Important Parameters In Vivo
Published on: September 26, 2016
Magnetic resonance studies of a redox probe in a reverse sodium bis(2-ethylhexyl)sulfosuccinate/octane/water
Daniel A Binks1, Neil Spencer, John Wilkie
1School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT.
Abstract:
The location and dynamics of the [Ru(bpy)(3)](2+) complex inside sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/octane/water microemulsions were studied, over a range of droplet sizes, using magnetic resonance spectroscopy, dynamic light scattering, and molecular modeling. The T(1) magnetic resonance relaxation times of water inside the AOT reverse micelles (RMs) were measured in both the presence and the absence of the [Ru(bpy)(3)](2+) complex. Large size droplet RMs (ω(0) > 20) were found to be sensitive to the presence of the [Ru(bpy)(3)](2+) complex, which was detected through a decrease in the T(1) relaxation time of the water inside the RM core, as compared to RMs containing no [Ru(bpy)(3)](2+). However, no difference in T(1) relaxation time was observed for water in small RMs (ω(0) < 20). Two-dimensional (1)H-(1)H NOESY spectroscopy was performed to probe the location of the [Ru(bpy)(3)](2+) complex in both small (ω(0) = 9.2) and large droplets (ω(0) = 34.9). Cross-peaks between protons in the AOT tail groups and bipyridyl ligands were observed, showing that the [Ru(bpy)(3)](2+) complex resided in the RM interface. Finally, molecular modeling simulations were performed to probe the location of the [Ru(bpy)(3)](2+) complex and the structure of the RM. Molecular dynamics simulations confirmed the location of the [Ru(bpy)(3)](2+) complex in the RM interface and detected differences in the surfactant layer and the amount of water penetration into this layer with changing droplet size.

