A new iridium boride, β-IrB, was synthesized under high-pressure/high-temperature conditions of 10.5 GPa and 1500 °C in a multianvil press with a Walker-type module. The new modification β-IrB crystallizes in a new structure type in the orthorhombic space group Pnma (no. 62) with the lattice parameters a = 10.772(2) Å, b = 2.844(1) Å, and c = 6.052(2) Å with R1 = 0.0286, wR2 = 0.0642 (all data), and Z = 2. The structure was determined by single-crystal X-ray and neutron powder diffraction on samples enriched in B. The compound is built up by an alternating stacking of boron and iridium layers with the sequence ABA'B'. Additionally, microcalorimetry, hardness, and compressibility measurements of the binary iridium borides α-IrB, β-IrB, IrB, hexagonal IrB and orthorhombic IrB were carried out and theoretical investigations based on density function theory (DFT) were employed to complement a comprehensive evaluation of structure-property relations. The incorporation of boron into the structures does not enhance the compressibility but leads to a significant reduction of the bulk moduli and elastic constants in comparison to elemental iridium.
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http://dx.doi.org/10.1021/acs.inorgchem.8b01541 | DOI Listing |
Inorg Chem
December 2024
Department of Chemistry, Texas A&M University, College Station, Texas 77842, United States.
This work reports the synthesis of a bis(pyrrolylphosphino)phenyl borane (PBP)Ph () and its incorporation of Ir by metal insertion into B-Ph to afford the dipyrrolylboryl/bis(phosphine) pincer complex (PBP)Ir(Ph)Cl (). Hydrogenolysis of afforded (PBP)Ir(H)Cl (). Compound was converted into (PBP)IrCl () via reaction with -chlorosuccinimide, and exposure of to CO produced (PBP)IrCl(CO) ().
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering South China University of Technology, Wushan Rd-381, Guangzhou 510641, P.R. China.
Despite their significant importance, the challenges in direct and diverse synthesis of N-heterocyclic γ-amino acids/esters/ketones hamper exploration of their applications. Herein, by developing a multifunctional heterogeneous iridium single-atom catalyst composed of silica-confined iridium species and a boron-doped ZrO support (Ir-SAs@B-ZrO/SiO), we describe its utility in establishing a new reductive coupling reaction of N-heteroarenes and 1,2-dicarbonyls for selective and diverse construction of the as-described compounds in a straightforward manner. The striking features, including good substrate and functionality tolerance, high step and atom economy, exceptional catalyst reusability, and diversified product post-transformations, highlight the practicality of the developed chemistry.
View Article and Find Full Text PDFHeliyon
September 2024
Department of Environmental, Biological and Pharmaceutical Science and Technologies, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Dalton Trans
October 2024
Institute of Solid State Physics, TU Wien, A-1040 Vienna, Austria.
The binary boron-rich compounds α-IrB and β-IrB, formerly denoted as α- and β-IrB, were synthesized both arc melting followed by annealing at 800 °C (900 °C) and high-temperature thermal treatment of mixtures of the elements. X-ray structure analysis of α-IrB was performed on a single crystal (space group 2/, = 10.5515(11) Å, = 2.
View Article and Find Full Text PDFOrg Biomol Chem
July 2024
School of Pharmacy, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, UK.
The synthesis of the ethyl ester analogue of the ultrapotent antitumour antibiotic seco-duocarmycin SA has been achieved in eleven linear steps from commercially available starting materials. The DSA alkylation subunit can be made in ten linear steps from the same precursor. The route involves C-H activation at the equivalent of the C7 position on indole leading to a borylated intermediate 9 that is stable enough for peptide coupling reactions but can be easily converted to the free hydroxyl analogue.
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