98%
921
2 minutes
20
The 4f orbitals of Ce(IV) have shown appreciably enhanced covalent mixing with ligand orbitals relative to those of Ce(III). Here, X-ray spectroscopy, magnetic susceptibility measurements, and theoretical methods are used to investigate 4f covalency in CeF and CeCl. These techniques show covalent mixing between Ce 4f and F 2p orbitals to be about 25% less than mixing between Ce 4f and Cl 3p orbitals, placing CeF among the most ionic Ce(IV) compounds to-date. However, ligand field analysis using the experimental data shows significantly higher 4f orbital overlap with the F 2p orbitals compared to the Cl 3p. This result is counterintuitive since the Ce-F bonds display less 4f covalency despite their higher orbital overlap, and greater overlap is traditionally associated with enhanced bond covalency. The weaker covalency is attributed to the large energy gap between Ce 4f and F 2p orbitals strongly counteracting the higher orbital overlap. These results highlight that only a concerted consideration of both atomic orbital overlap and energy matching in f-element systems leads to an accurate picture of their bonding.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11421006 | PMC |
http://dx.doi.org/10.1021/jacs.4c07459 | DOI Listing |
J Mater Chem B
September 2025
Department of Chemistry, University of Waterloo, 200 University Ave. West, Waterloo, ON N2L 3G1, Canada.
Conjugated polymer nanoparticles (CPNs), especially poly(-phenylene ethynylene) nanoparticles (PPE-NPs), are promising candidates for bio-imaging due to their high photostability, adjustable optical characteristics, and biocompatibility. Despite their potential, the fluorescence mechanisms of these nanoparticles are not yet fully understood. In this work, we modeled a spherical PPE-NP in a water environment using 30 PPE dimer chains.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Department of Nuclear Safety and Environmental Engineering Technology, China Institute of Atomic Energy, Beijing, 102413, P. R. China.
The immobilization of radioactive cesium (Cs) within sodalite frameworks is a critical challenge in nuclear waste management. This study employs density functional theory and molecular dynamics simulations to investigate the structural evolution, thermodynamic stability, and bonding mechanisms of Cs-incorporated sodalite (NaCsAlSiOCl, 0 ≤ ≤ 8). Formation energy calculations reveal a concentration-dependent preference for Cs substitution, with a minimum of 0.
View Article and Find Full Text PDFWater Res
August 2025
Hubei Key Laboratory of Multi-media Pollution Cooperative Control in Yangtze Basin, Key Laboratory of Water & Wastewater Treatment (MOHURD), School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China. Electronic address:
Conventional cobalt spinel oxides, widely employed in advanced oxidation processes, suffer from limited catalytic activity due to competitive overlap of O 2p orbitals between tetrahedral (Co) and octahedral cobalt (Co). Furthermore, their narrow pH activity window near neutrality severely restricts environmental applicability. To address these limits, the theories of covalency competition and microenvironment modulation are introduced to simulate the catalytic process and propose optimization strategies.
View Article and Find Full Text PDFJ Hazard Mater
August 2025
School of Metallurgy and Environment, Central South University, Changsha 410083, China; State Key Laboratory of Advanced Metallurgy for Non-ferrous Metals, Changsha 410083, China; Chinese National Engineering Research Center for Control & Treatment of Heavy Metal Pollution, Changsha 410083, China.
The similar chemical behavior of metal elements in acidic wastewater remains a significant challenge for their deep separation. A key limitation lies in overcoming weak metal selectivity and low separation efficiency. Our study introduced an innovative regulation strategy to enhance the coordination selectivity, enabling the rapid precipitation of Fe and the efficient complexation of Cu.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Department of Chemistry and Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany.
A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-][1]benzothiophene (C-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films.
View Article and Find Full Text PDF