Elemental boron has evoked substantial interest owing to its chemical complexity in nature. It can form multicenter bonds due to its electron deficiency, which induces the formation of various stable and metastable allotropes. The search for allotropes is attractive for finding functional materials with fascinating properties. Using first-principles calculations with evolutionary structure search, we have explored boron-rich K-B binary compounds under pressure. A series of dynamically stable structures (2 KB, KB, KB, and KB) containing boron framework with open channels are predicted, which can possibly be synthesized under high pressure and high temperature conditions. After the removal of K atoms, we obtain four novel boron allotropes, -B, -B, -B, and -B, which exhibit dynamical, thermal, and mechanical stability at ambient pressure. Among them, -B contains an unusual B pentagonal bipyramid and appears in a bonding combination of seven-center-two-electron (7c-2e) B-B π bonds, which is the first time to be identified in three-dimensional boron allotropes. Interestingly, our calculation reveals that -B can act as a superconductor with a value of 29.1 K under ambient conditions.
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http://dx.doi.org/10.1039/d3cp00692a | DOI Listing |
Chemistry
January 2025
Departamento de Química Inorgánica, -, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universidad de Zaragoza - CSIC, 50009, Zaragoza, Spain.
Hexahydride OsH(PPr) (1) releases H to form the isomeric tetrahydrides 2 a and 2 b of general formula OsH(PPr). Tetrylenes E{N(SiMe)} (E=Ge, Sn) are able to selectively trap these isomers distinguishing between them. Tetrylene Ge{N(SiMe)} catches 2 b to generate OsH{Ge[N(SiMe)]}(PPr) (3), which has a piano stool geometry, while Sn{N(SiMe)} captures 2 a to give OsH{Sn[N(SiMe)]}(PPr) (4) with the donor atoms defining a pentagonal bipyramid around the osmium center.
View Article and Find Full Text PDFChem Asian J
January 2025
Department of Chemistry, Indian Institute of Technology, Bombay, Powai, 400076, Mumbai, India.
Isostructural Dy(III) and Er(III) complexes [L Ln(HO)][I] ⋅ L ⋅ (CHCl) (Ln=Dy (1), Er (3)) and [L Ln(HO)][I] ⋅ L ⋅ (CHCl) (Ln=Dy (2), Er (4)), with distorted pentagonal bipyramidal geometry (D) around the central metal were synthesized by utilizing two bulky phosphonamide ligands, adamantyl phosphonamide, (Ad)P(O)(NHPr) (L) and carbazolyl phosphoramide (Cz)P(O)(NHPr) (L). The resultant complexes were investigated for their magnetic properties in order to elucidate the impact of modification of the coordinating P-O bond environment either by increasing steric bulk and/or introduction of a third P-N bond at the central phosphorus atom. Magnetic studies revealed substantial energy barriers (U) of 640 K and 491 K for Dy compounds 1 and 2, respectively, rendering them as some of the best-performing air-stable SIMs amongst the class of SIMs with D symmetry.
View Article and Find Full Text PDFInorg Chem
December 2024
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Bldg 4, 31 Leninsky Prosp., Moscow 119071, Russian Federation.
Four new Np(V) perchlorate complexes of the composition [NpO(HO)]ClO (orthorhombic) (), [(NpO)(ClO)(HO)]ClO·HO (), [(NpO)(UO)(HO)](ClO) (), and [(NpO)Cl(HO)]ClO·2HO () have been synthesized and structurally characterized. The structure of previously known monoclinic modification of NpOClO·4HO () has been determined at 100 K. The coordination environment of Np and U atoms in compounds - is pentagonal bipyramids.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, Institute of Green Chemistry and Molecular Engineering, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, Sun Yat-Sen University, Guangzhou, 510006, P. R. China.
A photochromic dysprosium-based single-molecule magnet [Dy(CyPhPO)(HO)](PMoO) ⋅ 3CyPhPO⋅HO (1-Dy) is synthesized via cocrystal engineering of a polyoxomolybdate (POMo) anion and an Ising-type cation with pseudo pentagonal bipyramidal geometry. Upon ultraviolet irradiation, Mo-to-Mo single-electron photoreduction occurs in the POMo moiety, resulting in significant changes of optical and magnetic properties. The emergence of intervalence charge-transfer transitions in heteropoly blue state 1-Dy* facilitates photothermal conversion in near-infrared region.
View Article and Find Full Text PDFDysprosium single-molecule magnets (SMMs) with two mutually -anionic ligands have shown large crystal field (CF) splitting, giving record effective energy barriers to magnetic reversal ( ) and hysteresis temperatures ( ). However, these complexes tend to be bent, imposing a transverse field that reduces the purity of the projections of the CF states and promotes magnetic relaxation. A complex with only one charge-dense anionic ligand could have more pure CF states, and thus high and .
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