JACS: RESOLV PI Prof. G. Clever and his’s group revealed a reversible transformation in azulene-based coordination cages, driven by guest interaction, with potential for diagnostics and catalysis.

Targeted genetic channel modifications can protect hydrogen-producing enzymes from harmful oxygen.

Opt. Mater. Express: RESOLV member Prof. C. Saraceno's review discusses the challenging combination of high repetition rates and high average power simultaneously, focusing on intense ultra-broadband high repetition rate terahertz sources based on organic crystals

Angew. Chem. Int. Ed. : With RESOLV support, Prof. M. Hansmann and his team identified the strongest neutral nucleophiles to date—mesoionic olefins—topping the Mayr scale and opening new paths in catalysis

Water is a major driving force in the formation of separate reaction compartments within cells.

Angew. Chem. Int. Ed. : RESOLV members, Prof. Christian Merten and Prof. Lukas J. Gooßen present a new Pd-catalyzed Schöllkopf-type amino acid synthesis that enables direct conversion of abundant aryl chlorides into valuable arylglycines. Using methylnaphthyl(XPhos)-Pd catalyst, ZnCl₂, and a strong lithium base, the reaction proceeds at room temperature with up to 95% yield and excellent…

ChemSusChem: RESOLV PI, Prof. K. Tschulik, showed how aqueous electrolytes, aldehydes exist in three forms: The non-hydrated aldehyde, the diol, and the diolate. This studi highlights that all three species exhibit electroactivity. Hence, it is possible to formulate approaches for addressing the OH−-induced decomposition of aldehydes during the electrochemical oxidation of aldehydes.

Nat. Commun.: RESOLV PI's, Prof. K. Morgenstern, Prof. W. Sander and Prof. E. Sanchez-Garcia, in collaborative cooperation, show how to alter the chirality dynamics of a single molecule through tip-induced van der Waals interactions.

J. Am. Chem. Soc: The new sensor design resembles a molecular toolbox that can be used to quickly assemble sensors for a variety of purposes.

J. Org. Chem.: Two structurally related isomeric benzazirines show very different tunneling behaviors which demonstrate the influence of position isomerism on quantum tunneling rates.