RESUMO
We have studied the photoreaction of 1,2-diarylethenes under aerobic conditions in the presence of various amines to prevent side processes promoted by singlet oxygen. It has been found that the most amines quite effectively deactivate processes associated with singlet oxygen, but primary and secondary amines unlike tertiary ones, react with substrates resulting in various side products. Among the studied amines, the most effective additive for preventing side processes, including those associated with singlet oxygen is imidazole, which is practically not consumed in photoreaction. It was shown that imidazole can also prevents the photodegradation of organic photochromes in solutions. The results obtained can be used in various branches of science, technology and medicine to improve the photostability of photosensitive organics (dyes).
RESUMO
Thermal and photoinduced processes accompanying complexation of photochromic spiropyrans (SPP) with Zn ions in acetone solution were characterized by means of UV-vis and X-ray absorption spectroscopies in operando regime. SPP ligands are usually transparent at λ > 350 nm, but after mixing with Zn ions, they produce a stable colored (ε = 32 000-38 000 M-1 cm-1) complex with maximum absorption at 525 nm, which makes them a powerful tool for monitoring metal-ion concentration in solution. The complex revealed fluorescence and photochromic behavior under static irradiation with visible light with constant photoreaction quantum yield across its characteristic absorption band. Zn K-edge X-ray absorption spectra show prominent changes in Zn local atomic structure between free Zn ions and Zn complex. The pump-flow-probe scheme was adapted to measure operando changes in Zn coordination upon light irradiation. Within experimental time resolution, we have determined that 20 µs after light irradiation, Zn ion is released out of the complex. This is the first example of the direct spectroscopic probe of the Zn photorelease from the spiropyran complex.
