Borafluorene-Mediated Sulfur Activation: Isolation of Boryl-Linked S and S Catenates and Related Chalcogenide Molecules.

Although the activation of elemental sulfur by main group compounds is well-documented in the literature, the products of such reactions are often heterocyclic in nature. However, the isolation and characterization of sulfur catenates (i.e.

Efficient catalyst screening using graph neural networks to predict strain effects on adsorption energy.

Small-molecule adsorption energies correlate with energy barriers of catalyzed intermediate reaction steps, determining the dominant microkinetic mechanism. Straining the catalyst can alter adsorption energies and break scaling relationships that inhibit reaction engineering, but identifying desirable strain patterns using density functional theory is intractable because of the high-dimensional search space. We train a graph neural network to predict the adsorption energy response of a catalyst/adsorbate system under a proposed surface strain pattern.

SELFIES and the future of molecular string representations.

Artificial intelligence (AI) and machine learning (ML) are expanding in popularity for broad applications to challenging tasks in chemistry and materials science. Examples include the prediction of properties, the discovery of new reaction pathways, or the design of new molecules. The machine needs to read and write fluently in a chemical language for each of these tasks.

N-Heterocyclic Carbene-Assisted Reversible Migratory Coupling of Aminoborane at Magnesium.

A combined synthetic and theoretical investigation of N-heterocyclic carbene (NHC) adducts of magnesium amidoboranes is presented, which involves a rare example of reversible migratory insertion within a normal valent s-block element. The reaction of (NHC)Mg(N(SiMe ) ) (1) and dimethylamine borane yields the tris(amide) adduct (NHC-BN)Mg(NMe BH )(N(SiMe ) ) (2; NHC-BN = NHC-BH NMe ). In addition to Me N=BH capture at the C-Mg bond, mechanistic investigations suggest the likelihood of aminoborane migratory insertion from an RMg(NMe BH NMe BH ) intermediate.

Benchmarking the Fluxional Processes of Organometallic Piano-Stool Complexes.

The correlation consistent Composite Approach for transition metals (ccCA-TM) and density functional theory (DFT) computations have been applied to investigate the fluxional mechanisms of cyclooctatetraene tricarbonyl chromium ((COT)Cr(CO)) and 1,3,5,7-tetramethylcyclooctatetraene tricarbonyl chromium, molybdenum, and tungsten ((TMCOT)(CO) ( = Cr, Mo, and W)) complexes. The geometries of (COT)Cr(CO) were fully characterized with the PBEPBE, PBE0, B3LYP, and B97-1 functionals with various basis set/ECP combinations, while all investigated (TMCOT)(CO) complexes were fully characterized with the PBEPBE, PBE0, and B3LYP methods. The energetics of the fluxional dynamics of (COT)Cr(CO) were examined using the correlation consistent Composite Approach for transition metals (ccCA-TM) to provide reliable energy benchmarks for corresponding DFT results.

High-throughput search for magnetic and topological order in transition metal oxides.

The discovery of intrinsic magnetic topological order in MnBiTe has invigorated the search for materials with coexisting magnetic and topological phases. These multiorder quantum materials are expected to exhibit new topological phases that can be tuned with magnetic fields, but the search for such materials is stymied by difficulties in predicting magnetic structure and stability. Here, we compute more than 27,000 unique magnetic orderings for more than 3000 transition metal oxides in the Materials Project database to determine their magnetic ground states and estimate their effective exchange parameters and critical temperatures.

Tailoring Electronic and Optical Properties of MXenes through Forming Solid Solutions.

Alloying is a long-established strategy to tailor properties of metals for specific applications, thus retaining or enhancing the principal elemental characteristics while offering additional functionality from the added elements. We propose a similar approach to the control of properties of two-dimensional transition metal carbides known as MXenes. MXenes (MX) have two sites for compositional variation: elemental substitution on both the metal (M) and carbon/nitrogen (X) sites presents promising routes for tailoring the chemical, optical, electronic, or mechanical properties of MXenes.

Machine Learning-Enabled Design of Point Defects in 2D Materials for Quantum and Neuromorphic Information Processing.

Engineered point defects in two-dimensional (2D) materials offer an attractive platform for solid-state devices that exploit tailored optoelectronic, quantum emission, and resistive properties. Naturally occurring defects are also unavoidably important contributors to material properties and performance. The immense variety and complexity of possible defects make it challenging to experimentally control, probe, or understand atomic-scale defect-property relationships.

Planar, Stair-Stepped, and Twisted: Modulating Structure and Photophysics in Pyrene- and Benzene-Fused N-Heterocyclic Boranes.

Because of their rigidity, polycyclic aromatic hydrocarbons (PAHs) have become a significant building block in molecular materials chemistry. Fusion or doping of boron into PAHs is known to improve the optoelectronic properties by reducing the LUMO energy level. Herein, we report a comprehensive study on the syntheses, structures, and photophysical properties of a new class of fused N-heterocyclic boranes (NHBs), pyrene- and benzene-linked in a "Janus-type" fashion (2-4, 6-9, and 11).

Accurate First-Principles Calculation of the Vibronic Spectrum of Stacked Perylene Tetracarboxylic Acid Diimides.

π-stacked organic electronic materials are tunable light absorbers with many potential applications in optoelectronics. The optical properties of such molecules are highly dependent on the nature and energy of electron-hole pairs or excitons formed upon light absorption, which in turn are determined by intra- and intermolecular electronic and vibrational excitations. Here, we present a first-principles approach for describing the optical spectrum of stacked organic molecules with strong vibronic coupling.

Synthesis of MoVAlC MAX Phase and Two-Dimensional MoVC MXene with Five Atomic Layers of Transition Metals.

MXenes are a family of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides with a general formula of MXT, in which two, three, or four atomic layers of a transition metal (M: Ti, Nb, V, Cr, Mo, Ta, etc.) are interleaved with layers of C and/or N (shown as X), and T represents surface termination groups such as -OH, ═O, and -F. Here, we report the scalable synthesis and characterization of a MXene with five atomic layers of transition metals (MoVCT), by synthesizing its MoVAlC MAX phase precursor that contains no other MAX phase impurities.

Extremely twisted and bent pyrene-fused N-heterocyclic germylenes.

The first examples of pyrene-fused Janus-type N-heterocyclic germylenes (NHGe) are reported. Remarkably, the pyrene linker and the germanium containing rings are extremely twisted, with "twist angles" up to 64°. Coordination of a Lewis base modifies the twisting of pyrene to an overall bent core (141° bend angle).

Engineering Magnetic Phases in Two-Dimensional Non-van der Waals Transition-Metal Oxides.

The family of 2D magnetic materials is continuously expanding because of the rapid discovery of exfoliable van der Waals magnetic systems. Recently, the synthesis of non-van der Waals magnetic "hematene" from common iron ore has opened an unconventional route to 2D material discovery. These non-van der Waals 2D systems are chemically stable and easily available and may have different or enhanced properties compared to their van der Waals counterparts.

Engineering Zero-Dimensional Quantum Confinement in Transition-Metal Dichalcogenide Heterostructures.

Achieving robust, localized quantum states in two-dimensional (2D) materials like graphene is desirable for optoelectronics and quantum information yet challenging due to the difficulties in confining Dirac fermions. Traditional colloidal nanoparticle and epitaxially grown quantum dots are also impractical for solid-state devices, due to either complex surface chemistry, unreliable spatial positioning, or lack of electrical and optical access. In this work, we design and optimize nanoscale monolayer transition-metal dichalcogenide (TMD) heterostructures to natively host massive Dirac fermion bound states.

Prediction of Synthesis of 2D Metal Carbides and Nitrides (MXenes) and Their Precursors with Positive and Unlabeled Machine Learning.

Growing interest in the potential applications of two-dimensional (2D) materials has fueled advancement in the identification of 2D systems with exotic properties. Increasingly, the bottleneck in this field is the synthesis of these materials. Although theoretical calculations have predicted a myriad of promising 2D materials, only a few dozen have been experimentally realized since the initial discovery of graphene.

Universal fluctuations in growth dynamics of economic systems.

The growth of business firms is an example of a system of complex interacting units that resembles complex interacting systems in nature such as earthquakes. Remarkably, work in econophysics has provided evidence that the statistical properties of the growth of business firms follow the same sorts of power laws that characterize physical systems near their critical points. Given how economies change over time, whether these statistical properties are persistent, robust, and universal like those of physical systems remains an open question.

Surface-Engineered MXenes: Electric Field Control of Magnetism and Enhanced Magnetic Anisotropy.

Controlling magnetism in two-dimensional (2D) materials via electric fields and doping enables robust long-range order by providing an external mechanism to modulate magnetic exchange interactions and anisotropy. In this report, we predict that transition metal carbide and nitride MXenes are promising candidates for controllable magnetic 2D materials. The surface terminations introduced during synthesis act as chemical dopants that influence the electronic structure, enabling controllable magnetic order.

Tuning Noncollinear Spin Structure and Anisotropy in Ferromagnetic Nitride MXenes.

Recent experimental success in the realization of two-dimensional magnetism has invigorated the search for low-dimensional material systems with tunable magnetic anisotropy that exhibit intrinsic long-range ferromagnetic order. Here we report that modifying the surface termination and transition metal in monolayer MNT nitride MXenes gives rise to a rich diversity of noncollinear spin structures and finely tunable magnetocrystalline anisotropy. Based on first-principles simulations, we predict that manipulating the strength of the spin-orbit interaction and electron localization via the chemical degrees of freedom can induce sufficient anisotropy to counteract thermal fluctuations that suppress long-range magnetic order.

Prediction of Enhanced Catalytic Activity for Hydrogen Evolution Reaction in Janus Transition Metal Dichalcogenides.

Significant efforts have been made in improving the hydrogen evolution reaction (HER) catalytic activity in transition metal dichalcogenides (TMDs), which are promising nonprecious catalysts. However, previous attempts have exploited possible solutions to activate the inert basal plane, with little improvement. Among them, the most successful modification requires a careful manipulation of vacancy concentration and strain simultaneously.

Prediction of optimal structural water concentration for maximized performance in tunnel manganese oxide electrodes.

Crystal water has been shown to stabilize next-generation energy storage electrodes with structural tunnels to accommodate cation intercalation, but the stabilization mechanism is poorly understood. In this study, we present a simple physical model to explain the energetics of interactions between the electrode crystal lattice, structural water, and electrochemically cycled ions. Our model is applied to understand the effects of crystal water on sodium ion intercalation in a tunnel manganese oxide structure, and we predict that precisely controlling the crystal water concentration can optimize the ion intercalation voltage and capacity and promote stable cycling.

Tunable Magnetism and Transport Properties in Nitride MXenes.

Two-dimensional materials with intrinsic and robust ferromagnetism and half-metallicity are of great interest to explore the exciting physics and applications of nanoscale spintronic devices, but no such materials have been experimentally realized. In this study, we predict several MNT nitride MXene structures that display these characteristics based on a comprehensive study using a crystal field theory model and first-principles simulations. We demonstrate intrinsic ferromagnetism in MnNT with different surface terminations (T = O, OH, and F), as well as in TiNO and CrNO.

Heparinoids activate a protease, secreted by mucosa and tumors, via tethering supplemented by allostery.

Activation by glycosaminoglycans (GAGs) is an emerging trend among extracellular proteases important in disease. ProMMP-7, the zymogen of a matrix metalloproteinase secreted by mucosal epithelial and tumor cells, is activated at their surfaces by sulfated GAGs, but how? ProMMP-7 is activated in trans by representative heparin oligosaccharides in a length-dependent manner, with a large jump in activation at lengths of 16 monosaccharides. Imaging by atomic force microscopy visualized small complexes of proMMP-7 molecules linked by 8-mer lengths of heparinoids and extended assembles formed with 16-mer lengths of heparin.

Dynamic structure of the translocon SecYEG in membrane: direct single molecule observations.

Purified SecYEG was reconstituted into liposomes and studied in near-native conditions using atomic force microscopy. These SecYEG proteoliposomes were active in translocation assays. Changes in the structure of SecYEG as a function of time were directly visualized.