Synergistic Excited State involved Catalytic Reduction of (NH3-trz)[Fe(dipic)2] Complex by SnO2/TiO2 Nanocomposite

The photocatalytic activity of well-fabricated, economical SnO2/TiO2 nanocomposite synthesized via hydrothermal route was validated using the (NH3-trz)[Fe(dipic)2] complex under ultra-violet illumination. The structural features of (NH3-trz)[Fe(dipic)2] complex was explored in detail. The catalysts were systematically examined with XRD, SEM, FT-IR UV-vis, PL, micro-Raman, VSM, AFM, HRTEM. The photoreactivity of the model compound (NH3-trz)[Fe(dipic)2] in water/binary solvent systems was investigated. The rate of photoreaction (k) of nanocomposite (0.1432 sec-1) is higher than the SnO2 (0.0373 sec-1) and TiO2 (0.1422 sec-1) in H2O:PriOH (70:30%) than the rest of the solvents system. The pathways, mechanistic feature of accumulated reactive species on nanocomposite to induce adherent [Fe(dipic)2]- anion and photo-reductive products were studied. The generation of hydroxyl radical on the surface of each catalyst can be identified as 7-hydroxycoumarin and discussed.

Frontier molecular orbital engineering in spiro-based molecules: achieving aggregation induced delayed fluorescence for non-doped OLEDs

Frontier molecular orbital engineering has been demonstrated to achieve aggregation induced delayed fluorescence (AIDF) for non-doped OLEDs. As a proof of concept, a new model compound AT-spiro-DMACF is reported on...

Selective ozone activation of phenanthrene in liquid CO2

Facile phenanthrene (as a polyaromatic model compound) ozonolysis to oxygenated material precursors has been demonstrated in liquid CO2.

Effect of solvent type on the formation rate of benzyl cation intermediate in acidolysis of lignin

The purpose of this study was to examine how the type of solvent among aqueous 1,4-dioxane, tetrahydrofuran, ethanol, iso-propyl alcohol, or ethylene glycol and its content (mol%) affect the formation rate of benzyl cation intermediate (BC) in the acidolysis of lignin, using a simple model compound, 1,2-dimethoxy-4-methoxymethylbenzene. Because the BC forms from the model compound via two steps, i.e., protonation of the benzyl methoxymethyl group as the pre-equilibrium step and liberation of the methanol as the rate-determining step, the observed variation of the formation rate with type of solvent and solvent content originates from the effects on both steps undistinguishably. The formation rate of BC decreased with increasing mol% of any of the organic solvents for a range of relatively low mol%, but increased with it for relatively high mol%. The formation rate varied more in the ether than in the alcohol systems. These results seem to be regulated by the effect of changing the mol% on the pre-equilibrium step, i.e., on the proton activity, rather than on the rate-determining step. Two reaction products, 4-alkoxymethyl-1,2-dimethoxybenzene and 4-hydroxymethyl-1,2-dimethoxybenzene, exclusively formed in the aqueous alcohol systems. The former compound was confirmed to be thermodynamically more stable and kinetically the more favorable product.