APPLICATION OF PHOTOLYSIS AND ADSORPTION PRECONCENTRATION TO THE SPECTROPHOTOMETRIC DETERMINATION OF RUTHENIUM AND OSMIUM IN SOLUTIONS OF CARBONYL-COMPLEXES
Ea. Zakharchenko et al., APPLICATION OF PHOTOLYSIS AND ADSORPTION PRECONCENTRATION TO THE SPECTROPHOTOMETRIC DETERMINATION OF RUTHENIUM AND OSMIUM IN SOLUTIONS OF CARBONYL-COMPLEXES, Journal of analytical chemistry, 52(6), 1997, pp. 528-531
The behavior of carbonyl complexes of ruthenium and osmium in chloride
solutions under exposure to UV light was studied by electronic absorp
tion spectra and electron paramagnetic resonance. It was found that, u
nder exposure to UV light, the M-CO bond (M = Ru, Os) breaks according
to the reaction described previously for nitroso complexes. On the ba
sis of electronic absorption spectra measured in solutions of complexe
s during exposure to UV light, it was revealed that the quantum yield
of photoreaction products in hydrochloric acid solutions decreases in
the following order: [RuCOCl5](2-) > [RuNOCl5](2-) > [OsCOCl5](2-). A
procedure for the spectrophotometric determination of ruthenium and os
mium complexes with multiply bonded ligands using exposure to UV light
is developed. The adsorption of carbonyl and nitroso complexes of rut
henium and osmium by various adsorbents was studied as a function of t
he temperature and the concentration of HCl. It was found that the ads
orption proceeds according to the anion-exchange mechanism. Conditions
for preconcentration of nitroso and carbonyl complexes of ruthenium a
nd osmium by the POLIORGS-IV-N adsorbent were chosen. Conditions for q
uantitative desorption of [RuCOCl5](2-) with thiourea used as an eluan
t were determined. A procedure for the adsorption-spectrophotometric d
etermination of carbonyl complexes of ruthenium using exposure to UV l
ight with the detection limit of ruthenium as low as 0.02 mu g/mL and
an analytical range from 0.02 to 0.45 mu g/mL is developed.