Molecular Models of Atomically Dispersed Uranium at MoS2 Surfaces Reveal Cooperative Mechanism of Water Reduction.

Single atoms of uranium supported on molybdenum sulfide surfaces (U@MoS2) have been recently demonstrated to facilitate the hydrogen evolution reaction (HER) through electrocatalysis. Theoretical calculations have predicted uranium hydroxide moieties bound to edge-sulfur atoms of MoS2 as a proposed transition state involved in the HER process. However, the isolation of relevant intermediates involved in this process remains a challenge, rendering mechanistic hypotheses unverified. The present work describes the isolation and characterization of a uranium-hydroxide intermediate on molybdenum sulfide surfaces using [(Cp*3Mo3S4)UCp*], a molecular model of a reduced uranium center supported at MoS2. Mechanistic investigations highlight the metalloligand cooperativity with uranium involved in the water activation pathway. The corresponding uranium-oxo analogue, [(Cp*3Mo3S4)Cp*U(═O)], was also accessed from the hydroxide cluster via hydrogen atom transfer and from [(Cp*3Mo3S4)UCp*] through an alternative direct oxygen atom transfer. These results provide an atomistic perspective on the reactivity of low-valent uranium at molybdenum sulfide surfaces toward water, modeling key intermediates associated with the HER of U@MoS2 catalysts.

Molybdenum sulphide clusters as redox-active supports for low-valent uranium.

The preparation of an actinide substituted cubane cluster, (Cp*3Mo3S4)Cp*UI2, and its reduced derivatives are reported. Structural and spectroscopic investigations provide insight into the unique interactions between the actinide and its redox-active molybdenum sulphide metalloligand, serving as a model to study atomically-dispersed, low-valent actinide ions on MoS2 surfaces. To probe the ability of the assembly to facilitate multielectron small molecule activation, the reactivity of the fully-reduced cluster, (Cp*3Mo3S4)Cp*U, with azobenzene was investigated. Addition of the substrate results in the formation of a cis-bis-imido cluster, (Cp*3Mo3S4)Cp*U(NPh)2. Cooperative reactivity between the actinide and redox-active support facilitates the 4e--reduction of substrate.

A Proton-Responsive Pyridyl(benzamide)-Functionalized NHC Ligand on Ir Complex for Alkylation of Ketones and Secondary Alcohols.

A Cp*Ir(III) complex (1) of a newly designed ligand L1 featuring a proton-responsive pyridyl(benzamide) appended on N-heterocyclic carbene (NHC) has been synthesized. The molecular structure of 1 reveals a dearomatized form of the ligand. The protonation of 1 with HBF4 in tetrahydrofuran gives the corresponding aromatized complex [Cp*Ir(L1 H)Cl]BF4 (2). Both compounds are characterized spectroscopically and by X-ray crystallography. The protonation of 1 with acid is examined by 1 H NMR and UV-vis spectra. The proton-responsive character of 1 is exploited for catalyzing α-alkylation of ketones and ß-alkylation of secondary alcohols using primary alcohols as alkylating agents through hydrogen-borrowing methodology. Compound 1 is an effective catalyst for these reactions and exhibits a superior activity in comparison to a structurally similar iridium complex [Cp*Ir(L2 )Cl]PF6 (3) lacking a proton-responsive pendant amide moiety. The catalytic alkylation is characterized by a wide substrate scope, low catalyst and base loadings, and a short reaction time. The catalytic efficacy of 1 is also demonstrated for the syntheses of quinoline and lactone derivatives via acceptorless dehydrogenation, and selective alkylation of two steroids, pregnenolone and testosterone. Detailed mechanistic investigations and DFT calculations substantiate the role of the proton-responsive ligand in the hydrogen-borrowing process.

Solvent- and Temperature-Dependent Assembly in Monolayer Films of a Ferrocene-Naphthyridine Hybrid on HOPG.

The formation of a monolayer film of bis-naphthyridyl ferrocene on highly oriented pyrolytic graphite (HOPG) at ambient conditions is demonstrated. The films are prepared by drop casting from different solvents. The microscopic structure of the films is understood using atomic force microscopy (AFM) and scanning tunnelling microscopy (STM). The analysis reveals two different types of Phases (I and II) in the films and the relative percentage of these phases depends on the nature of the solvents used for the preparation and the thermodynamical condition. Solvents like methanol, acetonitrile and DMF exclusively select Phase-I, whereas acetone and ethanol show a mix of both phases at room temperature. The different phases are formed by different conformers of the molecule. We also show that the selectivity of one of the phases over the other is related to the difference in the energetics for the formation of these phases.