Kinetic study on bimolecular photochemical quenching of tris(2,2'-bipyridyl)ruthenium(II) complex in water-ethylene glycol binary media.

The bimolecular photochemical quenching of the tris(2,2'-bipyridyl)ruthenium (II) complex by ferricyanide ions in water-ethylene glycol binary media was investigated using a spectrophotometric approach, as previously reported by our research group. Time-resolved spectroscopy revealed that dynamic photochemical quenching occurred via a diffusion-dominated pathway. The static quenching process was found to occur significantly when the concentration of ethylene glycol was greater than 40 wt%.

Elucidating the Quenching Mechanism of Tris(2,2'-bipyridyl)ruthenium(II) Complex in the Water-Glycerol Binary System Based on the Microscopic Structure of the Media.

Kinetic studies on the photochemical quenching reaction of the tris(2,2'-bipyridyl) ruthenium(II) complex ([Ru(bpy)]) in water-glycerol binary media were conducted based on the Einstein-Smoluchowski (E-S) theory. Dynamic and static quenching behaviors were analyzed by comparing results from time-resolved spectroscopy and emission spectroscopy. While the dynamic quenching reaction aligns well with the E-S theory, static quenching was observed, leading to a notable increase in the overall photoquenching reaction rate constant.

Reversible colour/luminescence colour changes of tetracyanoruthenium(II) complexes by sorption/desorption of water molecules in crystals.

We report colour/luminescence colour changes of M[Ru(bpy)(CN)] crystal (M = Ca, Sr, and Ba; bpy = 2,2'-bipyridine). The X-ray crystallographic study revealed that the crystals are constructed from linear-chains of {[Ru(bpy)(CN)][Ca(HO)]}, {[Ru(bpy)(CN)][Sr(HO)]}, and {[Ru(bpy)(CN)][Ba(HO)](μ-HO)}, respectively. Ru(II) complex linear chains and the hydrophilic channels composed of M ion and water along them enable reversible water sorption/desorption without collapse of crystals responsible for the colour change.

Polymorphic crystal approach to changing the emission of [AuCl(PPh3)2], analyzed by direct observation of the photoexcited structures by X-ray photocrystallography.

The photoexcited charge-transferred state of [AuCl(PPh(3))(2)] in a novel polymorphic crystal form was directly observed by X-ray photocrystallographic analysis. Its photoexcited state was completely different from the one generated in the known crystal of [AuCl(PPh(3))(2)]; the photoexcited bond-shrunk state was generated in the known crystal. This difference in the generated photoexcited state was clearly reflected by the difference in emission color.

Photocrystallographic analysis of [AuCl(PPh3)2] for elucidation of the crystal packing effect on the photophysical properties.

A metal-ligand bond shortening of [AuCl(PPh(3))(2)] by photoexcitation was analyzed by the photocrystallographic method in the unsolvated crystal. The gradual structural change of photoexcited and ground-state molecules with cooling explains the temperature dependence of the emission spectrum and the excited-state lifetime. Actually, on cooling, the ground-state molecular structure approached the excited-state structure.

Crystal Structure and Energy Transfer in Double-Complex Salts Composed of Tris(2,2'-bipyridine)ruthenium(II) or Tris(2,2'-bipyridine)osmium(II) and Hexacyanochromate(III).

In crystals of double-complex salts [M(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O (M(2+) = Ru(2+), Os(2+); bpy = 2,2'-bipyridine), luminescence from (3)CT state of [M(bpy)(3)](2+) is partially quenched by [Cr(CN)(6)](3)(-) at 77 K and room temperature (RT). This quenching is attributed to intermolecular excitation energy transfer from the (3)CT state of [M(bpy)(3)](2+) to the (2)E(g) state of [Cr(CN)(6)](3)(-).