Search results for "phosphine oxides"

showing 5 items of 5 documents

New chiral α-aminophosphine oxides and sulfides: an unprecedented rhodium-catalyzed ligand epimerization

2001

International audience; New chiral α-aminophosphine oxide N,P(O) and sulfide N,P(S) ligands have been prepared in one-pot syntheses by addition of Ph2PH to (S)-PhCH[double bond, length half m-dash]NCH(Ph)CH3, followed by oxidation with O2 or S8. Crystallization from cold methanol leads to the isolation of an enantiomerically pure single N,P(O) diastereomer and to a 1 : 1 mixture of the two N,P(S) diastereomers. The coordination chemistry of these ligands with [RhCl(COD)]2 and [RhCl(CO)2]2 has been investigated under argon and syngas. At high temperatures, a P–C oxidative addition of the N,P(O) ligand followed by imine elimination leads to several hydrido rhodium species. The complexes conta…

AminophosphinesIminechemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisCoordination complexRhodiumCatalysischemistry.chemical_compoundEpimerizationMaterials ChemistryOrganic chemistryRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistrychemistry.chemical_classification010405 organic chemistryLigandPhosphine oxides and sulfidesDiastereomerGeneral ChemistryOxidative addition0104 chemical scienceschemistryHydroformylationHydroformylation
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α-Aminophosphonates, Phosphinates, and Phosphine Oxides as Extraction and Precipitation Agents for Rare Earth Metals, Thorium, and Uranium : A Review

2022

α-Aminophosphonates, -phosphinates, and -phosphine oxides are a group of organophosphorus compounds that were investigated as extraction agents for rare earth (RE) metals and actinoids for the first time in the 1960s. However, more systematic investigations of their extraction properties towards REs and actinoids were not started until the 2010s. Indeed, recent studies have shown that these α-amino-functionalized compounds can outperform the commercial organophosphorus extraction agents in RE separations. They have also proven to be very efficient extraction and precipitation agents for recovering Th and U from RE concentrates. These actinoids coexist with REs in some of the commercially im…

actinoidssaostusseparationα-aminophosphinatesrare earth elementsprecipitationharvinaiset maametallitrecoveryuuttoerotusmenetelmätα-aminophosphine oxidesextractionfosforiα-aminophosphonates
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Applications and stereoselective syntheses of P-chirogenic phosphorus compounds.

2016

International audience; Phosphorus compounds bearing chirality on the P-center are usually qualified as P-chirogenic or P-stereogenic. This chemical class concerns natural products, agrochemistry, molecular materials, biology and pharmacy, although it is certainly in coordination chemistry and in asymmetric catalysis using chiral transition metal complexes that P-chirogenic phosphorus compounds are the most used. The chiral phosphine ligands and their uses in asymmetric metal-catalyzed reactions have been widely reviewed in literature. However, an overview covering the applications as well as the stereoselective syntheses of all classes of phosphorus compounds has not yet been provided. Thi…

chemistry.chemical_elementring-closing metathesis010402 general chemistryenantioselective transfer hydrogenation[ CHIM ] Chemical Sciences01 natural sciencesCoordination complexcatalyzed asymmetric hydrogenationchemistry.chemical_compoundactive phosphine oxides[CHIM]Chemical Scienceschiral diphosphine ligandsOrganic chemistryMolecular materialstransition-metal catalysischemistry.chemical_classificationacyl-transfer catalysts010405 organic chemistryPhosphorusEnantioselective synthesisc migration rearrangementGeneral Chemistry0104 chemical scienceschemistrytert-butylphenylphosphine oxideStereoselectivityray crystal-structureChirality (chemistry)PhosphineChemical Society reviews
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Benson group additivity values of phosphines and phosphine oxides: Fast and accurate computational thermochemistry of organophosphorus species

2018

Composite quantum chemical methods W1X-1 and CBS-QB3 are used to calculate the gas phase standard enthalpy of formation, entropy, and heat capacity of 38 phosphines and phosphine oxides for which reliable experimental thermochemical information is limited or simply nonexistent. For alkyl phosphines and phosphine oxides, the W1X-1, and CBS-QB3 results are mutually consistent and in excellent agreement with available G3X values and empirical data. In the case of aryl-substituted species, different computational methods show more variation, with G3X enthalpies being furthest from experimental values. The calculated thermochemical data are subsequently used to determine Benson group additivity …

organophosphorus speciesEmpirical dataphosphine oxideslämpökemiaThermodynamics010402 general chemistry01 natural sciencesHeat capacitychemistry.chemical_compoundAdditive function0103 physical sciencesThermochemistrythermochemistryta116AlkylQuantum chemicalchemistry.chemical_classification010304 chemical physicsGeneral Chemistrylaskennallinen kemiaStandard enthalpy of formation0104 chemical sciencesComputational MathematicsphosphineschemistryPhosphineJournal of Computational Chemistry
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Benson group additivity values of phosphines and phosphine oxides : Fast and accurate computational thermochemistry of organophosphorus species

2019

Composite quantum chemical methods W1X-1 and CBS-QB3 are used to calculate the gas phase standard enthalpy of formation, entropy and heat capacity of 38 phosphines and phosphine oxides for which reliable experimental thermochemical information is limited or simply nonexistent. For alkyl phosphines and phosphine oxides, the W1X-1 and CBS-QB3 results are mutually consistent and in excellent agreement with available G3X values and empirical data. In the case of aryl-substituted species, different computational methods show more variation, with G3X enthalpies being furthest from experimental values. The calculated thermochemical data are subsequently used to determine Benson group additivity co…

organophosphorus speciesphosphinesphosphine oxideslämpökemialaskennallinen kemia
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