Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(12), С. 3753 - 3753
Опубликована: Янв. 1, 2024
Язык: Английский
Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(12), С. 3753 - 3753
Опубликована: Янв. 1, 2024
Язык: Английский
Journal of the American Chemical Society, Год журнала: 2024, Номер unknown
Опубликована: Дек. 17, 2024
Recent studies in transition metal catalysis employing chelating phosphines have suggested a role for partial ligand oxidation formation of the catalytically active species, with potentially widespread relevance number catalytic systems. We examine internal redox reaction PdII(bisphosphine)X2 (X = Cl, OAc, etc.) complexes to reveal previously underexplored aspects bisphosphine monoxides (BPMOs), including evaluation structure and development general conditions access collection structurally diverse BPMO precatalysts based on organopalladium oxidative addition complexes. In particular, series PdII(BPMO)(R)(X) (R aryl, alkyl; X I, Br) bearing 24 different ligands were characterized by NMR X-ray crystallography. Comparison performance versus as is demonstrated be an enabling diagnostic tool Pd development. Finally, differences behavior between monoxide rationalized through solid-state parametrization stoichiometric experiments.
Язык: Английский
Процитировано
2Опубликована: Авг. 7, 2024
Recent studies in transition metal catalysis employing chelating phosphines have suggested a role for partial ligand oxidation formation of the catalytically active species, with potentially widespread relevance number cata-lytic systems. We examine internal redox reaction PdII(bisphosphine)X2 (X = Cl, OAc, etc.) complexes to reveal previously underexplored aspects bisphosphine mono-oxides (BPMOs), including evaluation structure and development general conditions access collection structurally diverse BPMO precatalysts based on organopalladium oxidative addition complexes. In particular, series PdII(BPMO)(R)(X) (R=Aryl, Alkyl; X=I, Br) bearing 24 different ligands were characterized by NMR X-ray crystallog-raphy. Comparison catalytic performance phosphine versus bisphos-phine as is demonstrated be an enabling diagnostic tool Pd develop-ment. Finally, differences behavior between mono-oxide rationalized through solid-state parametrization stoichiometric experiments.
Язык: Английский
Процитировано
1ChemCatChem, Год журнала: 2024, Номер 16(22)
Опубликована: Авг. 17, 2024
Abstract Phosphine oxides are an interesting class of compounds possessing tetracoordinate and pentavalent phosphorus atoms have been employed in a wide range applications including reagents organic synthesis, metal extractants, flame retardants, pharmaceuticals, bioactivity studies. Among all, the degree basicity phosphoryl oxygen driven by nature substituents influences electronic properties central complex toward diversified catalytic processes. Further, presence heteroatoms adjacent to atom enhances nucleophilicity atom. In view this, present review covers past two decades remarkable versatility P=O‐based complexes describes governing factors influencing structural resultant coordination behavior. Interestingly, some P=O bond distances either longer or shorter compared their free ligands, indicating activity. These can effectively catalyze chemical reactions polymerizations, C−C Si−C activations, oxidation, reduction, hydroformylation, hydrophosphination, hydrogenation cyclization reactions. Furthermore, this emphasizes impact substituents, solvents, additives, light, temperature on efficiency.
Язык: Английский
Процитировано
1Organic Letters, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 18, 2024
A regioselective radical α,γ-diphosphinylation of allylamines with secondary phosphine oxides by photoinduced cobaloxime catalysis is described. The reaction tolerates a wide range and oxides, affording α-amino diphosphine dioxides in moderate to good yields hydrogen evolution. synthesis new monoxide ligands the promising antitumor activities products demonstrate great potential applications this approach drug discovery. detailed mechanism studies indicate that likely proceeds through dehydrogenative allylic phosphinylation nucleophilic addition process.
Язык: Английский
Процитировано
1Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(12), С. 3753 - 3753
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
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