Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 123436 - 123436
Published: Nov. 1, 2024
Language: Английский
Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 123436 - 123436
Published: Nov. 1, 2024
Language: Английский
Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(12), P. 7005 - 7010
Published: March 15, 2023
Tris(bicyclo[1.1.1]pentyl)phosphine can be prepared by radical addition of PH3 to [1.1.1]propellane, giving the smallest tri-tert-alkylphosphine known. PBcp3 is substantially smaller than PCy3 and comparable in electron-donating power PEt3. It gives a bis-ligated Pd(0) complex Pd(PBcp3)2 that exceptionally reactive toward alkyl halide oxidative functions as general ligand for palladium-catalyzed cross-coupling sp3 electrophiles. Radical [1.1.1]propellane phenylphosphine bis(bicyclo[1.1.1]pentyl)phosphine derivative PBcp2Ph, illustrating generality this approach bicyclopentylphosphine synthesis.
Language: Английский
Citations
12Digital Discovery, Journal Year: 2024, Volume and Issue: 3(8), P. 1467 - 1495
Published: Jan. 1, 2024
This review discusses the use of automation for organometallic reactions to generate rich datasets and, with statistical analysis and reaction component parameterisation, how mechanisms can be probed gain understanding.
Language: Английский
Citations
4Journal of Catalysis, Journal Year: 2023, Volume and Issue: 427, P. 115093 - 115093
Published: Aug. 9, 2023
Language: Английский
Citations
7Molecular Catalysis, Journal Year: 2024, Volume and Issue: 564, P. 114326 - 114326
Published: June 21, 2024
Language: Английский
Citations
1Brazilian Journal of Chemical Engineering, Journal Year: 2023, Volume and Issue: 41(1), P. 299 - 308
Published: April 3, 2023
Language: Английский
Citations
1Molecular Catalysis, Journal Year: 2024, Volume and Issue: 569, P. 114491 - 114491
Published: Sept. 6, 2024
Language: Английский
Citations
0ChemCatChem, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 27, 2024
Abstract Controlling the metal geometric and electronic structure is of significance in developing efficient catalysts for heterogeneous hydroformylation. This study examines structural sizes Rh + ‐Rh 0 distribution to construct a highly active catalyst formaldehyde The sites hydroformylation require several n atoms, while single‐atom can solely catalyze hydrogenation. highest activity was achieved on nanoclusters (0.95 nm), giving TOF 191 h −1 selectivity 82% glycolaldehyde formation. tunability properties synergistic interaction between are essential enhanced activity. Pseudo‐ situ FT‐IR analysis elucidated that adsorbed nanocluster prefers produce via hydroformylation, isolated δ+ tends form methanol provides new insight into design guidance understanding reaction mechanism aldehydes/olefins
Language: Английский
Citations
0Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 123436 - 123436
Published: Nov. 1, 2024
Language: Английский
Citations
0