Boosting the Formation of Brønsted Acids on Flame-made WOx/ZrO2 for Glucose Conversion.

WOx/ZrO2 with a higher concentration of Brønsted acid sites (BAS) and a bigger ratio of Brønsted to Lewis acid sites (B/L) than achievable by conventional impregnation (IM) were synthesized using flame spray pyrolysis (FSP). The rapid quenching and short residence time inherent to FSP prevent the accumulation of W atoms on the ZrO2 support and thus provide an excellent surface dispersion of WOx species. As a result, FSP-made WOx/ZrO2 (FSP-WOx/ZrO2) has a much higher surface concentration of three-dimensional Zr-WOx clusters than corresponding materials prepared by conventional impregnation (IM-WOx/ZrO2). The coordination of W-OH to the unsaturated Zr4+ sites in these clusters results in a remarkable decrease of the concentration of Lewis acid sites (LAS) on the surface of ZrO2 and promotes the formation of bridging W-O(H)-Zr hydroxyl groups acting as BAS. FSP-WOx/ZrO2 possesses ~80% of BAS and a B/L ratio of around 4, while IM-WOx/ZrO2 exhibits ~50% BAS and a B/L ratio of around 1. These catalysts were evaluated in the dehydration of glucose to HMF. The catalytic study demonstrated that B/L ratio plays a crucial role in glucose conversion. The best catalyst, FSP-WOx/ZrO2 with a W/Zr ratio of 1/10 affords nearly 100% glucose conversion and an HMF selectivity of 56-69%.

Modeling and Experimental Study of the Electron Transfer Kinetics for Non-ideal Electrodes Using Variable-Frequency Square Wave Voltammetry.

The knowledge of nonequilibrium electron transfer rates is paramount for the design of modern hybrid electrocatalysts. Herein, we propose a general simulation-based approach to interpret variable-frequency square wave voltammetry (VF-SWV) for heterogeneous materials featuring reversible redox behavior. The resistive and capacitive corrections, inclusion of the frequency domain, and statistical treatment of the surface redox kinetics are used to account for the non-ideal nature of electrodes. This approach has been validated in our study of CoII/CoI redox transformation for Co tetraphenylporphyrin (CoTPP) immobilized on carbon cloth and multiwalled carbon nanotubes (CNTs) - one of the most active heterogeneous molecular catalysts in carbon dioxide (CO2) electroreduction. It is demonstrated that the modeling of experimental data furnishes the capacitance of the surface double layer C, uncompensated resistance Ru, symmetry coefficients α, kinetic constants k0, and equilibrium redox potentials E0 in one experiment. Moreover, the proposed method yields a stochastic map of the redox kinetics rather than a single value, thus exposing the inhomogeneous nature of the electrochemically active layer. The computed parameters are in excellent agreement with the results of the classic methods such as cyclic voltammetry and fall in line with the reported CoTPP catalytic activity. Thus, VF-SWV is suitable for the study of high-level composites such as covalent organic frameworks and organometallic-CNT mixtures. The resulting insights into the electron transfer mechanisms are especially useful for the rational development of the catalyst-support interfaces and immobilization methods.

Substrate-Selective C-H Functionalization for the Preparation of Organosulfur Compounds from Crude Oil-Derived Components.

The direct utilization of a natural feedstock in organic synthesis is an utmost challenge because the selective production of one product from a mixture of starting materials requires unprecedented substrate selectivity. In the present study, a simple and convenient procedure is evaluated for the substrate-selective alkenylation of a single component in a mixture of organosulfur compounds. Pd-catalyzed alkenylation of two-, three-, four-, and five-component mixtures of crude oil-derived sulfur species led to the exclusive C-H functionalization of only one compound. The observed remarkable substrate selectivity opens new opportunities for sustainable organic synthesis.