We explore chemical reactions within pnictogens with an example of bismuth and nitrogen under extreme conditions. Understanding chemical reactions between Bi and N, elements representing the first and the last stable elements of the nitrogen group, and the physical properties of their compounds under ambient and high pressure is far from being complete. Here, we report the high-pressure high-temperature synthesis of orthorhombic BiN (S.G. #60) from Bi and N precursors at pressures above 40 GPa. Using synchrotron single-crystal X-ray diffraction on the polycrystalline sample, we solved and refined the compound's structure and studied its behavior and compressibility on decompression to ambient pressure. We confirm the stability of BiN to pressures as low as 12.5(4) GPa. Below that pressure value, a group-subgroup phase transformation occurs, resulting in the formation of a non-centrosymmetric BiN solid with a space group 2 (S.G. #29). We use calculations to characterize the polymorphs of BiN. They also provide support and explanation for our experimental observations, in particular those corresponding to peculiar Bi-N bond evolution under pressure, resulting in a change in the coordination numbers of Bi and N as a function of pressure within the explored stability field of BiN.
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http://dx.doi.org/10.3389/fchem.2023.1257942 | DOI Listing |
J Phys Chem A
December 2024
College of Chemistry and Materials Science, Hebei Key Laboratory of Inorganic Nano-Materials, Hebei Normal University, Shijiazhuang 050024, China.
Halogen, chalcogen, pnictogen, and tetrel bonds in organocatalysis have gained noticeable attention. In this work, carbon-bromide bond activation in the Ritter reaction by bidentate imidazole-type halogen, chalcogen, pnicogen, and tetrel bond donors was studied by density functional theory. All of the above four kinds of catalysts exhibited excellent catalytic performance.
View Article and Find Full Text PDFChem Rec
December 2024
Department of Chemistry, Universidade Federal de Minas Gerais (UFMG), 31.270-901, Belo Horizonte, MG, Brazil.
Alkylation reactions and their products are considered crucial in various contexts. Synthetically, the alkylation of a nucleophile is usually promoted using hazardous alkyl halides. Here, we aim to highlight the potential of pnictogen (ammonium or phosphonium) and chalcogen salts (sulfonium, selenonium, and telluronium) to function as alkylating agents.
View Article and Find Full Text PDFChemistry
January 2025
Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada.
Two homologous series of pnictogen(III) dications, stabilized by 2,6-bis(benzimidazole-2-yl)pyridine ligands have been prepared. Both series contain Pn-X moieties (Pn = P, As, Sb, Bi; X = Cl or Ph) and have been fully characterized using spectroscopic methods including X-ray crystallography. The Lewis acidity of these compounds has also been probed by computational methods; the results suggest that the dictations are strong Lewis acids, with the PnCl compounds being more acidic than the PnPh compounds, and with Lewis acidity increasing from P to Bi, in both series.
View Article and Find Full Text PDFChem Commun (Camb)
October 2024
Department of Chemistry, Brock University, 1812 Sir Isaac Brock Way, St., Catharines, ON, L2S 3A1, Canada.
Organochlorophosphonium P(V) species are strong Lewis acids deriving from a low-lying σ* orbital at P opposite to Cl. Herein, applying this strong acidity to heterogenous reactivity, we introduce polymer-supported phosphorus(V)-mediated Lewis acid catalysis. Key to this innovation is the use of a recyclable solid support Merrifield resin P(V) Lewis acid catalyst with demonstrated utility for the one-pot synthesis of sydnones.
View Article and Find Full Text PDFOrganometallics
June 2024
Department of Chemistry, Texas A&M University, PO Box 30012, College Station, Texas 77842-3012, United States.
Photolyses of -Fe(CO)(As((CH) )As) ( = , 10; , 12; , 14) in the presence of PMe, or reactions of -[Fe(CO)(NO)(As((CH) )As)] BF and -BuN Cl, afford the air stable title complexes As((CH) )As (-) in 79-34% yields. With , the , and , isomers are separable and each is crystallographically characterized. With ,, the isomers rapidly interconvert by homeomorphic isomerization, but each crystallizes (contrathermodynamically) as an , isomer.
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