Sulfur-Bridged Iron and Molybdenum Catalysts for Electrocatalytic Ammonia Synthesis.

Carbon zero electrocatalytic nitrogen reduction reaction (NRR), converting N to NH under ambient temperature and pressure, offers a sustainable alternative to the energy-intensive Haber-Bosch process. Nevertheless, NRR still faces major challenges due to direct dissociation of the strong N≡N triple bond, poor selectivity, as well as other issues related to the inadequate adsorption, activation and protonation of N. In nature's nitrogen fixation, microorganisms are able to convert N to ammonia at ambient temperature and pressure, and in aqueous environment, thanks to the nitrogenase enzymes.

Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes.

Dinuclear lanthanide complexes [((HB(pz))Dy)(μ-ThAn)] (1Dy) and [((HB(pz))Dy)(μ-ClCNAn)] (2Dy), based on the hydrotris(pyrazol-1-yl)borate (HBpz) scorpionate capping ligand and anilate (An) bridging linkers, namely homosubstituted dithiophene- and heterosubstituted chlorocyanoanilate, bearing electron-donating and withdrawing substituents at the 3,6-positions of the benzoquinone core, are reported. 1Dy shows an octacoordinated {NO} Dy ion within a distorted square antiprismatic coordination, an ideal geometry for Single-Molecule Magnet (SMM) behavior, given its oblate nature, whereas in 2Dy the octacoordinated Dy ion adopts a triangular dodecahedron geometry, while maintaining the same {NO} coordination sphere. Both complexes show field-induced single molecule magnet (SMM) behaviour, with tuning of the slow magnetic relaxation as a function of the nature of the substituents at the 3,6-positions of the anilate moiety.

Memory effect in ferroelectric polyvinylidene fluoride (PVDF) films spin crossover probes.

Ferroelectric polymers are of great interest due to their intrinsic processing capabilities, superior to classic inorganic ferroelectric materials. For example, polyvinylidene fluoride (PVDF) and derivatives have been incorporated into multiple device architectures for information storage and transfer. Here we report an additional advantage of organic ferroelectrics as their flexibility allows for the preparation of composites with spin crossover (SCO) probes to tune their ferroelectric parameters by external stimuli.

Cooperative Effects Drive Water Oxidation Catalysis in Cobalt Electrocatalysts through the Destabilization of Intermediates.

A barrier to understanding the factors driving catalysis in the oxygen evolution reaction (OER) is understanding multiple overlapping redox transitions in the OER catalysts. The complexity of these transitions obscure the relationship between the coverage of adsorbates and OER kinetics, leading to an experimental challenge in measuring activity descriptors, such as binding energies, as well as adsorbate interactions, which may destabilize intermediates and modulate their binding energies. Herein, we utilize a newly designed optical spectroelectrochemistry system to measure these phenomena in order to contrast the behavior of two electrocatalysts, cobalt oxyhydroxide (CoOOH) and cobalt-iron hexacyanoferrate (cobalt-iron Prussian blue, CoFe-PB).

Complementary probes for the electrochemical interface.

The functions of electrochemical energy conversion and storage devices rely on the dynamic junction between a solid and a fluid: the electrochemical interface (EI). Many experimental techniques have been developed to probe the EI, but they provide only a partial picture. Building a full mechanistic understanding requires combining multiple probes, either successively or simultaneously.

Structure and Electronic Properties of Large Oligomeric Heterometallic 3d/Ce Polyoxometalates.

Merging the rich chemistry of Ce(IV) polyoxometalates (POMs) with that of 3d polyanions remains a challenge due to the strong competition between these highly oxophilic lanthanide cations and 3d metallic ions for coordination to lacunary molecular metal oxides. We report herein the characterization of an unprecedented water stable hexameric Ce/Co POM () made of two {(SiW)Ce} units connected to a {(SiW)Co(PO)} core. In addition, the pentameric Ce/Ni compound , where two {PWNiW} and a {PWNi} fragments are grafted on a {(PW)Ce} moiety, has been obtained.

Terbium and Europium Chlorocyananilate-Based 2D Coordination Polymers.

Two-dimensional layered coordination polymers based on the hetero-substituted 3-chloro-6-cyano-2,5-dihydroxybenzoquinone ligands, hereafter ClCNAn anilate, and Ln ions (Tb and Eu) are reported. Compounds and , formulated as Ln(ClCNAn)(DMSO) (Ln = Tb, ; Eu, ), and their related intermediates and , formulated as Ln(ClCNAn)(HO)·yHO (x + y likely = 12, Ln = Tb, ; and Eu, ), were prepared by a conventional one-pot reaction (the latter) and recrystallized from DMSO solvent (the former). Polyhydrated intermediates and show very similar XRPD patterns, while, despite their common stoichiometry, and are not isostructural.

as a Versatile and Predictable Chiral Stationary Phase for the Resolution of Racemic Mixtures.

Metal-organic frameworks (MOFs) have become promising materials for multiple applications due to their controlled dimensionality and tunable properties. The incorporation of chirality into their frameworks opens new strategies for chiral separation, a key technology in the pharmaceutical industry as each enantiomer of a racemic drug must be isolated. Here, we describe the use of a combination of computational modeling and experiments to demonstrate that high-performance liquid chromatography (HPLC) columns packed with as the chiral stationary phase are efficient, versatile, robust, and reusable with a wide array of mobile phases (polar and non-polar).

Manipulating Intermetallic Charge Transfer for Switchable External Stimulus-Enhanced Water Oxidation Electrocatalysis.

Electrocatalytic processes involving the oxygen evolution reaction (OER) present a kinetic bottleneck due to the existence of linear-scaling relationships, which bind the energies of the different intermediates in the mechanism limiting optimization. Here, we offer a way to break these scaling relationships and enhance the electrocatalytic activity of a Co-Fe Prussian blue modified electrode in OER by applying external stimuli. Improvements of ≈11 % and ≈57 % were achieved under magnetic field (0.

Synthesis and characterization of highly diluted polyanionic iron(II) spin crossover systems.

Spin crossover (SCO) complexes, through their reversible spin transition under external stimuli, can work as switchable memory materials. Here, we present a protocol for the synthesis and characterization of a specific polyanionic iron SCO complex and its diluted systems. We describe steps for its synthesis and the determination of crystallographic structure of the SCO complex in diluted systems.

A quantum spin liquid candidate isolated in a two-dimensional CoRh bimetallic oxalate network.

A quantum spin liquid (QSL) is an elusive state of matter characterized by the absence of long-range magnetic order, even at zero temperature, and by the presence of exotic quasiparticle excitations. In spite of their relevance for quantum communication, topological quantum computation and the understanding of strongly correlated systems, like high-temperature superconductors, the unequivocal experimental identification of materials behaving as QSLs remains challenging. Here, we present a novel 2D heterometallic oxalate complex formed by high-spin Co(ii) ions alternating with diamagnetic Rh(iii) in a honeycomb lattice.

Separation of Volatile Organic Compounds in TAMOF-1.

Separation of volatile organic compounds is one of the most studied processes in industry. TAMOF-1 is a homochiral metal-organic framework with a crystalline network of interconnected ≈1 nm channels and has high thermal and chemical stability. Thanks to these features, it can resolve racemic mixtures of chiral drugs as a chiral stationary phase in chromatography.

Enhancement of electrocatalytic oxygen evolution by chiral molecular functionalization of hybrid 2D electrodes.

A sustainable future requires highly efficient energy conversion and storage processes, where electrocatalysis plays a crucial role. The activity of an electrocatalyst is governed by the binding energy towards the reaction intermediates, while the scaling relationships prevent the improvement of a catalytic system over its volcano-plot limits. To overcome these limitations, unconventional methods that are not fully determined by the surface binding energy can be helpful.

Lowering the Water Oxidation Overpotential by Spin-Crossover in Cobalt Hexacyanoferrate.

The oxygen evolution reaction (OER) is limited by the inherent linear scaling relationships of its reaction intermediates. Manipulating the spin configuration of the water oxidation intermediates allows us to overcome these constraints. Cobalt hexacyanoferrate (CoFe-PB) is an efficient and robust water oxidation catalyst and further known as a magnetic switch.

Synergic Bistability between Spin Transition and Fluorescence in Polyfluorene Composites with Spin Crossover Polymers.

In recent years, several examples of materials combining the molecular bistability of spin crossover (SC) and fluorescent moieties have flourished in the literature. Fluorescence is a sensitive probe, and SC may provide modulation of the signal, thus affording systems in which physicochemical changes in the environment of the SC centers could be effectively detected. On the contrary, organic semiconductor polymers are of great interest and, furthermore, have been successfully applied in different optoelectronic devices, such as transistors, solar cells, and light-emitting devices.

Crystal Structure and Magnetic Properties of Trinuclear Transition Metal Complexes (Mn, Co, Ni and Cu) with Bridging Sulfonate-Functionalized 1,2,4-Triazole Derivatives.

Here we present the synthesis, structure and magnetic properties of complexes of general formula (Mn)(MeNH)][Mn(μ-L)(HO)] and (MeNH)[M(μ-L)(HO)] (M = Co, Ni and Cu); L = 4-(1,2,4-triazol-4-yl) ethanedisulfonate). The trinuclear polyanions were isolated as dimethylammonium salts, and their crystal structures determined by single crystal and powder X-ray diffraction data. The polyanionic part of these salts have the same molecular structure, which consists of a linear array of metal(II) ions linked by triple N1-N2-triazole bridges.

Benchmarking Catalysts for Formic Acid/Formate Electrooxidation.

Energy production and consumption without the use of fossil fuels are amongst the biggest challenges currently facing humankind and the scientific community. Huge efforts have been invested in creating technologies that enable closed carbon or carbon neutral fuel cycles, limiting CO emissions into the atmosphere. Formic acid/formate (FA) has attracted intense interest as a liquid fuel over the last half century, giving rise to a plethora of studies on catalysts for its efficient electrocatalytic oxidation for usage in fuel cells.

Understanding polyoxometalates as water oxidation catalysts through iron cobalt reactivity.

Cobalt polyoxometalates (Co-POMs) have emerged as promising water oxidation catalysts (WOCs), with the added advantage of their molecular nature despite being metal oxide fragments. In comparison with metal oxides, that do not offer well-defined active surfaces, POMs have a controlled, discrete structure that allows for precise correlations between experiment and computational analyses. Thus, beyond highly active WOCs, POMs are also model systems to gain deeper mechanistic understanding on the oxygen evolution reaction (OER).

Differentiation of Epoxide Enantiomers in the Confined Spaces of an Homochiral Cu(II) Metal-Organic Framework by Kinetic Resolution.

TAMOF-1, a homochiral metal-organic framework (MOF) constructed from an amino acid derivative and Cu(II), was investigated as a heterogeneous catalyst in kinetic resolutions involving the ring opening of styrene oxide with a set of anilines. The branched products generated from the ring opening of styrene oxide with anilines and the unreacted epoxide were obtained with moderately high enantiomeric excesses. The linear product arising from the attack on the non-benzylic position of styrene oxide underwent a second kinetic resolution by reacting with the epoxide, resulting in an amplification of its final enantiomeric excess and a concomitant formation of an array of isomeric aminodiols.

Redefining the Mechanistic Scenario of Carbon-Sulfur Nucleophilic Coupling via High-Valent Cp*Co Species.

The potential access to Co species for promoting transformations that are particularly challenging at Co still remains underexploited in the context of Cp*Co-catalyzed C-H functionalization reactions. Herein, we disclose a combined experimental and computational strategy for uncovering the participation of Cp*Co species in a Cp*Co-mediated C-S bond-reductive elimination. These studies support the intermediacy of high-valent Cp*Co species in C-H functionalization reactions, under oxidative conditions, when involving nucleophilic coupling partners.

Nanostructured Photocatalysts for the Production of Methanol from Methane and Water.

The direct photocatalytic conversion of methane into methanol with water at room temperature and pressure has attracted particular attention in recent decades. Valuable insight has been obtained into the reaction mechanisms and the key descriptors that control photoactivity and selectivity. This Minireview highlights the different efforts that have been undergone on the design of nanostructured photocatalytic systems to enhance the selectivity to methanol.

Push-Pull Electronic Effects in Surface-Active Sites Enhance Electrocatalytic Oxygen Evolution on Transition Metal Oxides.

Sustainable electrocatalysis of the oxygen evolution reaction (OER) constitutes a major challenge for the realization of green fuels. Oxides based on Ni and Fe in alkaline media have been proposed to avoid using critical raw materials. However, their ill-defined structures under OER conditions make the identification of key descriptors difficult.