98%
921
2 minutes
20
The crystal structure of many inorganic compounds can be understood as a metallic matrix playing the role of a host lattice in which the nonmetallic atomic constituents are located, the Anions in Metallic Matrices (AMM) model stated. The power and utility of this model lie in its capacity to anticipate the actual positions of the guest atoms in inorganic crystals using only the information known from the metal lattice structure. As a pertinent test-bed for the AMM model, we choose a set of common metallic phases along with other nonconventional or more complex structures (face-centered cubic (fcc) and simple cubic Ca, CsCl-type BaSn, hP4-K, and fcc-Na) and perform density functional theory electronic structure calculations. Our topological analysis of the chemical pressure (CP) scalar field, easily derived from these standard first-principles electronic computations, reveals that CP minima appear just at the precise positions of the nonmetallic elements in typical inorganic crystals presenting the above metallic subarrays: CaF, rock-salt and CsCl-type phases of CaX (X = O, S, Se, Te), BaSnO, KS, and NaX (X = F, Cl, Br, I). A theoretical basis for this correlation is provided by exploring the equivalence between hydrostatic pressure and the oxidation (or reduction) effect induced by the nonmetallic element on the metal structure. Indeed, our CP analysis leads us to propose a generalized stress-redox equivalence that is able to account for the two main observed phenomena in solid inorganic compounds upon crystal formation: (i) the expansion or contraction experienced by the metal structure after hosting the nonmetallic element while its topology is maintained and (ii) the increasing or decreasing of the effective charge associated with the anions in inorganic compounds with respect to the charge already present in the interstices of the . We demonstrate that a rational explanation of this rich behavior is provided by means of Pearson-Parr's electronegativity equalization principle.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.inorgchem.9b01470 | DOI Listing |
J Phys Chem C Nanomater Interfaces
September 2025
Institute of Inorganic Chemistry of the Czech Academy of Sciences, Husinec-Řež 1001, 250 68 Řež, Czech Republic.
Coordination polymers (CPs) are versatile materials formed by metal ions and organic ligands, offering a broad range of structural and functional possibilities. Phosphonates and phosphinates are particularly attractive ligands for CPs due to their multiple binding sites, varied coordination geometries, and ability to form robust network structures. Phosphonates, considered harder ligands, form strong bonds with hard metals such as Fe, while phosphinates offer additional versatility due to the varied pendant groups on phosphorus.
View Article and Find Full Text PDFChem Sci
August 2025
Inorganic Solid State Chemistry, Saarland University Campus C4.1 66123 Saarbrücken Germany
Intermetallic compounds belong to an important class of materials, not only due to the sheer number of compounds known but also due to their application in everyday life. These compounds possess their very own peculiarities, especially when it comes to chemical bonding. To address this point, bonding analyses based on Crystal Orbital Bond Index (COBI) values, Löwdin charges, and - for the first time - oxidation numbers (ON ) were conducted, all extracted from delocalized plane-wave functions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK.
Organic molecular glasses are attractive matrices to disperse active ingredients in pharmaceuticals or electronic devices. Typically, they i) have lower glass transition temperatures than inorganic or polymeric glasses, making them easier to process, and ii) are less prone to phase segregation from other organic active materials. However, there is a dearth of functional groups that are known to induce glass formation in preference to crystallization.
View Article and Find Full Text PDFDalton Trans
September 2025
Section for Solid State and Theoretical Inorganic Chemistry, Institute of Inorganic Chemistry, Auf der Morgenstelle 18, 72076 Tübingen, Germany.
A series of niobium oxyiodide compounds has recently been identified using a non-conventional reduction method. The continuation of these studies of heterogeneous solid-state reactions in a closed system has led to the crystallization and structural analysis of two novel compounds LiNbOI and NbOI(NbI). Both crystal structures are derived from the pentanuclear [NbO] cluster core and are expanded through the incorporation of additional niobium atoms, forming new [NbO] and [NbO] cluster cores.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemistry, Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK.
Topochemical reduction of the n = 2 Ruddlesden-Popper oxide, LaSrCoRuO, yields LaSrCoRuO, a phase containing (Co/Ru)O squares which share corners to form 1D infinite double-chains. In contrast, fluorination of LaSrCoRuO yields the oxyfluoride LaSrCoRuOF, which can then be reduced to form LaSrCoRuOF. This reduced oxyfluoride is almost isoelectronic with LaSrCoRuO, but LaSrCoRuOF has a crystal structure in which the (Co/Ru)O squares are connected into 2D infinite sheets.
View Article and Find Full Text PDF