Synthesis of some fluorinated thiazolopyridine from pentafluoropyridine and 4-phenylsulfonyl tetrafluoropyridine [PDF]
In this study, the reaction of pentafluoropyridine and 4-phenylsulfonyl tetrafluoropyridine with difunctional nitrogen and sulfur nucleophiles such as thiourea, thioamide derivatives, and unsymmetrical bidentate nitrogen nucleophiles such as diamino ...
Danesteh, Roghayeh +2 more
core +1 more source
2,3,5,6-Tetrafluoro-[N-(3-aminopropyl)-ε-caprolactam]-4-pyridine
The title compound was synthesized at a near-quantitative yield using the nucleophilic aromatic substitution of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) with perfluoropyridine (PFP). The purity and structure were determined by NMR (1H, 13C, 19F), GC-EIMS,
Chadron M. Friesen +2 more
doaj +1 more source
Dialkylamino compounds of group 14 elements (Si, Ge, Sn) in the +2 oxidation state supported by benzamidinate ligands were synthesized and treated with pentafluoropyridine.
Amit Pratap Singh (1958941) +6 more
core +1 more source
Transient isomerisation and inverse electronic relaxation of infrared multiple-photon excited Pentafluoropyridine [PDF]
Pentafluoropyridine (PFP) undergoes fast structural isomerisation to fulvenes when irradiated with 9R(16) CO2 laser line in the fluence range 0.5-1.5 J/cm2. The unstable fulvenes slowly decay back to PFP in ms time scale.
Chowdhury, P. K. +2 more
core +1 more source
Influence of the Diphosphine Coordinated to Molybdenum and Tungsten Triangular M3S4 Cluster Hydrides in the Catalytic Hydrodefluorination of Pentafluoropyridine [PDF]
Hydrido molybdenum and tungsten(IV) cluster cations of formula [M3S4H3(dppe)3]+ (dppe = 1,2-(bis)dimethylphosphinoethane), [Mo-1]+ (M = Mo) and [W-1]+ (M = W), have been isolated by reacting their halide precursors with borohydride.
Llusar, Rosa +3 more
core +1 more source
Amine‐Ligated Boryl Radicals Enables Direct C─F Borylation and Cross‐Couplings of Polyfluoroarenes
We present a synergistic strategy combining photocatalytic direct C─F borylation of polyfluoroarenes with Suzuki–Miyaura cross‐coupling. The high nucleophilicity of amine‐ligated boryl radicals enables efficient homolytic aromatic substitution of polyfluoroarenes, forming stable amine–borane adducts that resist protodeboronation and can be directly ...
Naoki Yasukawa +8 more
wiley +2 more sources
Speciation‐Controlled C–F Bond Functionalization Enabled by Zwitterionic Pnictinidenes
Zwitterionic pnictinidenes turn C–F activation into C–X bond construction, enabling broad defluorinative functionalization of polyfluoro(hetero)arenes under mild conditions. Rather than following a metallomimetic Sb(I)/Sb(III) redox turnover, catalysis is redirected by ligand scrambling into a redox‐neutral manifold, revealing catalyst speciation as a ...
Irene Sánchez‐Sordo +4 more
wiley +1 more source
Main Group Metals in Redox Catalysis
Main group metal redox catalysis is emerging as a credible alternative to transition metal chemistry. Elements from groups 13 to 15 now enable diverse catalytic manifolds, driven by ligand design and control of electronic structure. This review highlights recent advances, key design principles, and remaining challenges, positioning main group metals as
Olympia Mouriki +2 more
wiley +1 more source
Trigonal Phosphine Umpolung: Electrophilicity Driven by a Redox‐Active Boron Cluster
Coupling of a phosphine to a redox‐active cluster enables polarity reversal, or umpolung, at phosphorus. Phosphines are classically known for their nucleophilicity, and while electrophilic reactivity has been observed in geometrically constrained, non‐trigonal systems, similar behavior in ordinary trigonal phosphines is rare.
Bryce C. Nussbaum +2 more
wiley +1 more source
In this study, novel polymer/graphene oxide (GO) composites were engineered for the adsorption and recovery of phenolic compounds from olive mill wastewater.
Naila Mraieh +9 more
doaj +1 more source

