Search results for "Phosphinidene"

showing 8 items of 8 documents

Preparation and Characterization of P2 BCh Ring Systems (Ch=S, Se) and Their Reactivity with N-Heterocyclic Carbenes

2018

Four-membered rings with a P2BCh core (Ch = S, Se) have been synthesized via reaction of phosphinidene chalcogenide (Ar*P=Ch) and phosphaborene (Mes*P=BNR2). The mechanistic pathways towards these rings are explained by detailed computational work that confirmed the preference for the formation of P–P, not P–B, bonded systems, which seems counterintuitive given that both phosphorus atoms contain bulky ligands. The reactivity of the newly synthesized heterocycles, as well as that of the known (RPCh)n rings (n = 2, 3), was probed by the addition of Nheterocyclic carbenes, which revealed that all investigated compounds can act as sources of low-coordinate phosphorus species. peerReviewed

BOND COVALENT RADIIChalcogenidePHOSPHINIDENE ADDUCTSSULFURchemistry.chemical_element010402 general chemistryRing (chemistry)ION ABSTRACTION01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundELEMENTSmain-group heterocyclesReactivity (chemistry)N-heterocyclic carbenesMETHYLENEPHOSPHINEta116epäorgaaniset yhdisteetphosphinidene chalcogenidesheterocycleskemiallinen synteesiphosphaborenes010405 organic chemistryPhosphorusOrganic ChemistryGeneral ChemistryREAGENT0104 chemical sciencesCharacterization (materials science)PHOSPHORUSchemistryPhosphinideneinorganic compoundsSULFURIZATIONchemical synthesisX-RAY-STRUCTUREChemistry - A European Journal
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CCDC 224280: Experimental Crystal Structure Determination

2004

Related Article: J.Vicente, J.-A.Abad, R.Clemente, J.Lopez-Serrano, M.C.Ramirez de Arellano, P.G.Jones, D.Bautista|2003|Organometallics|22|4248|doi:10.1021/om0303552

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(NNN'N'-tetramethylethylenediamine)-(2-(2-triphenylphosphinideneamino)phenyl-12-bis(methoxycarbonyl)ethenyl)-palladium(ii) perchlorate deuterochloroform solvateExperimental 3D Coordinates
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CCDC 224279: Experimental Crystal Structure Determination

2004

Related Article: J.Vicente, J.-A.Abad, R.Clemente, J.Lopez-Serrano, M.C.Ramirez de Arellano, P.G.Jones, D.Bautista|2003|Organometallics|22|4248|doi:10.1021/om0303552

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates(NNN'N'-tetramethylethylenediamine)-(2-(triphenylphosphinideneamino)phenyl)-(triphenylphosphine)-palladium(ii) trifluoromethanesulfonate
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CCDC 224276: Experimental Crystal Structure Determination

2004

Related Article: J.Vicente, J.-A.Abad, R.Clemente, J.Lopez-Serrano, M.C.Ramirez de Arellano, P.G.Jones, D.Bautista|2003|Organometallics|22|4248|doi:10.1021/om0303552

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterschloro-(5-methyl-2-triphenylphosphinideneaminophenyl)-mercuryExperimental 3D Coordinates
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Insertion Reactions of Neutral Phosphidozirconocene Complexes as a Convenient Entry into Frustrated Lewis Pair Territory

2016

International audience; Neutral phosphidozirconocene complexes [Cp2Zr(PR2)Me] (Cp=cyclopentadienyl; 1a: R=cyclohexyl (Cy); 1b: R=mesityl (Mes); 1c: R=tBu) undergo insertion into the Zr-P bond by non-enolisable carbonyl building blocks (O=CRR), such as benzophenone, aldehydes, paraformaldehyde or CO2, to give [Cp2Zr(OCRRPR2)Me] (3-7). Depending on the steric bulk around P, complexes 3-7 react with B(C6F5)(3) to give O-bridged cationic zirconocene dimers that display typical frustrated Lewis pair (FLP)/ambiphilic ligand behaviour. Thus, the reaction of {[Cp2Zr(-OCHPhPCy2)][MeB(C6F5)(3)]}(2) (10a) with chalcone results in 1,4 addition of the Zr+/P FLP, whereas the reaction of {[Cp2Zr(-OCHFcPCy…

Steric effectsChalconeStereochemistryzirconiumc-h activation010402 general chemistry01 natural sciencesMedicinal chemistry[ CHIM ] Chemical SciencesCatalysisFrustrated Lewis pairinsertionchemistry.chemical_compoundCyclopentadienyl complexx-ray structuresphosphinidene complexesBenzophenone[CHIM]Chemical SciencesParaformaldehydezr-p bondzirconocene-phosphido complexesmolecular-structure010405 organic chemistryLigandphosphidesOrganic ChemistryCationic polymerizationcrystal-structureGeneral Chemistry0104 chemical sciencesfunctionalized ligandsbis(trimethylsilyl)phosphido complexeschemistryfrustrated Lewis pairsphosphinoaryloxide complexesambiphilic ligands
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Trapping Rare and Elusive Phosphinidene Chalcogenides

2017

Four-membered rings with a P2Ch2 core (Ch=S, Se) and phosphorus in the +3 oxidation state have been synthesized. The utility of these rings as a source of monomeric phosphinidene chalcogenides was probed by the addition of an N-heterocyclic carbene, resulting in a base-stabilized phosphinidene sulfide. Similarly, persistence of the phosphinidene selenide in solution was shown through cycloaddition chemistry with 2,3-dimethylbutadiene at elevated temperatures. The observed reactivity was explained by detailed computational work that established the conditions upon which the P2Ch2 rings can liberate phosphinidene chalcogenides. peerReviewed

chemistry.chemical_classificationSulfide010405 organic chemistryGeneral MedicineGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisCycloaddition0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPhosphinideneOxidation stateSelenidephosphinidenesReactivity (chemistry)ta116CarbeneAngewandte Chemie International Edition
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Phosphorus-Chalcogen Ring Expansion and Metal Coordination

2017

The reactivity of 4-membered (RPCh)2 rings (Ch = S, Se) that contain phosphorus in the +3 oxidation state is reported. These compounds undergo ring expansion to (RPCh)3 with the addition of a Lewis base. The 6-membered rings were found to be more stable than the 4-membered precursors, and the mechanism of their formation was investigated experimentally and by density functional theory calculations. The computational work identified two plausible mechanisms involving a phosphinidene chalcogenide intermediate, either as a free species or stabilized by a suitable base. Both the 4- and 6-membered rings were found to react with coinage metals, giving the same products: (RPCh)3 rings bound to the…

metal coordination010405 organic chemistryChemistryInorganic chemistryCoinage metals010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesInorganic ChemistryMetalCrystallographyChalcogenring expansionOxidation statePhosphinidenevisual_artvisual_art.visual_art_mediumReactivity (chemistry)Lewis acids and basesPhysical and Theoretical Chemistryphosphorus-chalcogenta116
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Proton reduction by phosphinidene-capped triiron clusters

2021

Bis(phosphinidene)-capped triiron carbonyl clusters, including electron rich derivatives formed by substitution with chelating diphosphines, have been prepared and examined as proton reduction catalysts. Treatment of the known cluster [Fe3(CO)9(µ3-PPh)2] (1) with various diphosphines in refluxing THF (for 5, refluxing toluene) afforded the new clusters [Fe3(CO)7(µ3-PPh)2(κ2-dppb)] (2), [Fe3(CO)7(µ3-PPh)2(κ2-dppv)] (3), [Fe3(CO)7(µ3-PPh)2(κ2-dppe)] (4) and [Fe3(CO)7(µ3-PPh)2(µ-κ2-dppf)] (5) in moderate yields, together with small amounts of the corresponding [Fe3(CO)8(µ3-PPh)2(κ1-Ph2PxPPh2)] cluster (x = -C4H6-, -C2H2-, -C2H4-, -C3H6-, -C5H4FeC5H4-). The molecular structures of complexes 3 a…

rautaphosphinidine010402 general chemistryElectrochemistry01 natural sciencesBiochemistryMedicinal chemistryRedoxproton reductionDFTCatalysisInorganic Chemistrychemistry.chemical_compoundkatalyytitelektrokatalyysiDiphosphinesMaterials ChemistryCluster (physics)electrocatalysisPhysical and Theoretical Chemistryfosfori010405 organic chemistryLigandOrganic ChemistrytiheysfunktionaaliteoriakompleksiyhdisteettriironToluene0104 chemical scienceschemistryPhosphinidene
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