Isolation and characterization of the dimetal decacarbonyl dication [Ru(CO)] and the metal-only Lewis-pair [Ag{Ru(CO)}] .

The reaction of Ag with Ru(CO) in a CO atmosphere under concommittant irradiation with UV-light yields a salt of the metal-only Lewis-pair [Ag{Ru(CO)}]. Switching the silver cation for a more process-selective deelectronator yields a salt of the homoleptic transition metal carbonyl cation [Ru(CO)], which fills the gap between the known cations [Ru(CO)] and [Ru(CO)]. The amount of π-backdonation in this series was studied by a combination of vibrational spectroscopy and computed relaxed force constants.

Pushing redox potentials to highly positive values using inert fluorobenzenes and weakly coordinating anions.

While the development of weakly coordinating anions (WCAs) received much attention, the progress on weakly coordinating and inert solvents almost stagnated. Here we study the effect of strategic F-substitution on the solvent properties of fluorobenzenes CFH (xFB, x = 1-5). Asymmetric fluorination leads to dielectric constants as high as 22.

OCT1 (SLC22A1) transporter kinetics and regulation in primary human hepatocyte 3D spheroids.

3D spheroids of primary human hepatocytes (3D PHH) retain a differentiated phenotype with largely conserved metabolic function and proteomic fingerprint over weeks in culture. As a result, 3D PHH are gaining importance as a model for mechanistic liver homeostasis studies and in vitro to in vivo extrapolation (IVIVE) in drug discovery. However, the kinetics and regulation of drug transporters have not yet been assessed in 3D PHH.

Synthesis and Characterization of a Copper Dinitrogen Complex Supported by a Weakly Coordinating Anion.

We report the synthesis and full characterization of the copper dinitrogen complex [(η-N)Cu{Al(OR)}] 2 (R=C(CF)) prepared by a cascade metathesis reaction of Ag[Al(OR)] with CuI-excess in iso-perfluorohexane (i-pfh) under N atmosphere. Title compound 2 features an extraordinarily high N stretching frequency at 2313/2314 cm (IR/Raman) and was characterized by single-crystal and powder X-ray diffractometry. Quantum chemical charge displacement analysis based on natural orbitals of chemical valence (CD-NOCV) indicates that the copper-dinitrogen interaction is still governed by weak π-backdonation, but is significantly reduced compared to all literature-known transition metal dinitrogen complexes.

Utilizing the Perfluoronaphthalene Radical Cation as a Selective Deelectronator to Access a Variety of Strongly Oxidizing Reactive Cations.

A selective deelectronation reagent with very high potential of +2.00 (solution)/+2.41 V (solid-state) vs.