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Metal hexafluorides hydrolyze at ambient temperature to deposit compounds having fluorine-to-oxygen ratios that depend upon the identity of the metal. Uranium-hexafluoride hydrolysis, for example, deposits uranyl fluoride (UO2F2), whereas molybdenum hexafluoride (MoF6) and tungsten hexafluoride deposit trioxides. Here, we pursue general strategies enabling the prediction of depositing compounds resulting from multi-step gas-phase reactions. To compare among the three metal-hexafluoride hydrolyses, we first investigate the mechanism of MoF6 hydrolysis using hybrid density functional theory (DFT). Intermediates are then validated by performing anharmonic vibrational simulations and comparing with infrared spectra [McNamara et al., Phys. Chem. Chem. Phys. 25, 2990 (2023)]. Conceptual DFT, which is leveraged here to quantitatively evaluate site-specific electrophilicity and nucleophilicity metrics, is found to reliably predict qualitative deposition propensities for each intermediate. In addition to the nucleophilic potential of the oxygen ligands, several other contributing characteristics are discussed, including amphoterism, polyvalency, fluxionality, steric hindrance, dipolar strength, and solubility. To investigate the structure and composition of pre-nucleation clusters, an automated workflow is presented for the simulation of particle growth. The workflow entails a conformer search at the density functional tight-binding level, structural refinement at the hybrid DFT level, and computation of a composite free-energy profile. Such profiles can be used to estimate particle nucleation kinetics. Droplet formation is also considered, which helps to rationalize the different UO2F2 particle morphologies observed under varying levels of humidity. Development of predictive methods for simulating physical and chemical deposition processes is important for the advancement of material manufacturing involving coatings and thin films.
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http://dx.doi.org/10.1063/5.0176552 | DOI Listing |
Phys Chem Chem Phys
September 2025
College of Ecology and Environment, Inner Mongolia University, Hohhot, 010021, China.
This investigation explores the impact of an external electric field (EEF) in the normal-direction on cyclo[18]carbon, scrutinizing changes in molecular conformation, electronic structure, reactivity, and spectroscopic properties. Utilizing Gaussian16 and Multiwfn, we modeled the molecule under EEF conditions. The EEF induced an expansion of the cyclo[18]carbon ring and increased bond lengths.
View Article and Find Full Text PDFRSC Adv
August 2025
Laboratory of Applied Physics, Department of Physics, Faculty of Sciences of Sfax, University of Sfax Sfax Tunisia.
The mechanistic pathway of the (3 + 2) cycloaddition (32CA) between azomethine ylide 1 and dimethyl acetylenedicarboxylate 2, affording 4-isoxazoline derivatives, was elucidated Density Functional Theory (DFT) calculations employing the B3LYP-D3 functional and the 6-311++G(d,p) basis set in 1,4-dioxane. Reactivity insights derived from Conceptual DFT (CDFT) demonstrated that compound 1 behaves as an ambiphilic species with significant nucleophilic and electrophilic tendencies, whereas compound 2 functions predominantly as an electrophile. These electronic features reveal a marked polarity in the cycloaddition and align with a forward electron density flux (FEDF) governing the reaction process.
View Article and Find Full Text PDFInorg Chem
August 2025
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Moscow 119991, Russia.
Malonate ligands demonstrate versatility for intercalating metal complexes into layered rare-earth hydroxides (LREHs), enabling controlled tuning of coordination geometry and composition. As a proof of concept, a series of copper(II) malonate complexes with various substituents was synthesized and successfully intercalated into layered yttrium, europium, or terbium hydroxide at room temperature via anion-exchange reactions. The copper content in these hybrid materials increased in the order: butylmalonate < benzylmalonate < cyclopropanedicarboxylate < dimethylmalonate.
View Article and Find Full Text PDFUltrason Sonochem
September 2025
College of Mining Engineering, North China University of Science and Technology, Tangshan 063210, China. Electronic address:
Blast furnace dust (BFD) represents a significant processing residue in the steel manufacturing. The clean and efficient utilization of BFD could not only alleviate zinc resource shortage but also hold great significance for the resource recycling of steel enterprises. This study investigated the behavior and kinetics of zinc leaching from BFD with crotonic acid as a novel reagent under ultrasonic conditions.
View Article and Find Full Text PDFArtif Photosynth
July 2025
Department of Physics and Astronomy, Purdue University, West Lafayette, Indiana 47907, United States.
Optimization of water oxidation reaction (WOR) catalysts is critical for the development of clean energy technology based on the concept of artificial photosynthesis. Deep mechanistic insights at the molecular and electronic levels are required. Theoretically, the radical coupling (RC) mechanism should allow for a virtually barrier-less process of O-O bond formation in the WOR.
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