Overcoming Pd Catalyst Deactivation in the C-H Coupling of Tryptophan Residues in Water Using Air as the Oxidant.

The Pd-catalyzed C-H activation of natural tryptophan residues has emerged as a promising approach for their direct synthetic modification. While using water as the solvent and harnessing air as the oxidant is enticing, these conditions induce catalyst deactivation by promoting the formation of inactive Pd(0) clusters. In this work, we have studied optimized Pd-based catalytic systems via nonsteady state kinetic analysis and in situ X-ray absorption spectroscopy (XAS) to overcome catalyst deactivation, which enables the effective use of lower Pd loadings.

Adsorption of PFAS by All-Silica Zeolite ß: Insights into the Effect of the Water Matrix, Regeneration of the Material, and Continuous PFAS Adsorption.

Per- and polyfluoroalkyl substances (PFAS) are man-made organic compounds ubiquitously present in the environment. Due to their persistency and bioaccumulative nature, and because of increasingly stringent regulations of PFAS, their removal from the environment is necessary. Our initial study identified all-silica zeolite ß as an alternative adsorbent with a high selectivity, affinity, and capacity for perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) removal. Here, we study the influence of the PFAS chain length on the affinity and capacity of a novel material, all-silica zeolite ß, showing that the *BEA zeolite is an ideal sorbent for the removal of PFAS with 8 carbons. The solution pH and the addition of cations or natural organic substances to the water matrix have minimal influence on PFOA/PFOS removal with the zeolite. Next, regeneration of a PFOS-loaded zeolite was assessed; besides thermal, solvent-driven regeneration of the zeolite is also possible, using well-selected combinations of non-noxious solvents. Lastly, continuous adsorption experiments show that zeolite can be used for larger-scale applications.