Thermal stability, photochromic sensitivity and optical properties of [Ru(bpy)(2)(OSOR)]+ compounds with R = Bn, BnCl, BnMe
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Updated: Jun 5, 2026

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
Published on: October 31, 2019
Volker Dieckmann1, Kristin Springfeld, Sebastian Eicke
1Department of Physics, University of Osnabrück, Barbarastr 7, 49069 Osnabrück, Germany. vdieckma@uos.de
Abstract:
The influence of ligand substitution on the photochromic properties of [Ru(bpy)(2)(OSOR)]∙PF(6) compounds (bpy = 2,2'-bipyridine, OSO = 2-methylsulfinylbenzoate) dissolved in propylene carbonate is studied by UV/VIS laser-spectroscopy as a function of temperature and exposure. The group R is either Bn (CH(2)C(6)H(5)), BnCl or BnMe. The photochromic properties originate from a phototriggered linkage isomerization located at the SO ligand. It is shown that the thermal stability of the studied compounds can be varied by ligand substitution in the range of 1.6 × 10(3) s to 3.9 × 10(4) s. In contrast, absorption spectra of ground and metastable states as well as the characteristic exposure of the photochromic response remain unchanged. The results are explained in the frame of photoinduced linkage isomerization located at the SO ligand.
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