Search results for "STRUCTURAL-CHARACTERIZATION"

showing 6 items of 6 documents

Input of P, N-(phosphanyl, amino)-ferrocene hybrid derivatives in late transition metals catalysis

2018

International audience; Unequally functionalized ferrocenes give access to valuable hemilabile reactivity in catalytic reaction. We address the synthesis of hybrid (P, N)-ferrocenyl compounds for which recent catalytic breakthrough applications have been reported, transversely in late transition metals chemistry. Palladium, nickel, rhodium, iridium, and emerging iron and gold catalysis are illustrated from selected examples, which include CC bond formation from cross-coupling and polymerization, allylic substitution, cyanation, hydroformylation, CH arylation and silylation and hydrogenation reactions.

Allylic rearrangementnickel-complexesAminophosphinesethylene oligomerizationchemistry.chemical_elementHomogeneous catalysispbeta-ketoestersCyanation[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryn ligands01 natural sciencesRhodiumCatalysisInorganic ChemistryPolymer chemistryoxazoline-containing ligandsMaterials ChemistryOrganic chemistry[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryPolyfunctionalized ligandsferrocenyl ligands010405 organic chemistryasymmetric catalysisHemilabile hybridsHomogeneous catalysischiral ligandssimple ketones0104 chemical scienceschemistrystructural-characterizationFerroceneHydroformylationPalladiumLate transition metals
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Direct experimental observation of mesoscopic fluorous domains in fluorinated room temperature ionic liquids

2017

Fluorinated room temperature ionic liquids (FRTILs) represent a class of solvent media that are attracting great attention due to their IL-specific properties as well as features stemming from their fluorous nature. Medium-to-long fluorous tails constitute a well-defined apolar moiety in the otherwise polar environment. Similarly to the case of alkyl tails, such chains are expected to result in the formation of self-assembled fluorous domains. So far, however, no direct experimental observation has been made of the existence of such structural heterogeneities on the nm scale. We report here the first experimental evidence of the existence of mesoscopic spatial segregation of fluorinated dom…

General Physics and AstronomyNanotechnology02 engineering and technologyNeutron scattering010402 general chemistryLAYER CAPACITOR APPLICATIONS; PERFLUOROALKYL SIDE-CHAINS; ANGLE NEUTRON-SCATTERING; PARTICLE MESH EWALD; PHYSICOCHEMICAL PROPERTIES; FORCE-FIELD; CATION SYMMETRY; STRUCTURAL-CHARACTERIZATION; AMMONIUM TETRAFLUOROBORATE; MOLECULAR SIMULATION01 natural sciencesionic liquidsionic liquids SANS nanostructuration fluorous domains NMR NOEchemistry.chemical_compoundMolecular dynamicsPhysics and Astronomy (all)nanostructurationMoietyPhysical and Theoretical ChemistryAlkylNOEchemistry.chemical_classificationfluorous domainsMesoscopic physicsSANSNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyNMR0104 chemical sciencesfluorinated ionic liquids neutron scattering x-ray diffraction structurechemistryChemical physicsIonic liquidPolar0210 nano-technology
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Copper(I) Complexes of Bis(2-(diphenylphosphino)phenyl) Ether:  Synthesis, Reactivity, and Theoretical Calculations

2007

The tricoordinated cationic Cu-I complex [Cu(kappa(2)-P,P'-DPEphos)(kappa(1)-P-DPEphos)][BF4] (1) (DPEphos = bis(2-(diphenylphosphino)phenyl) ether) containing a dangling phosphorus center was synthesized from the reaction of [Cu(CH3CN)(4)][BF4] with DPEphos in a 1:2 molar ratio in dichloromethane. When complex 1 is treated with MnO2, elemental sulfur, or selenium, the uncoordinated phosphorus atom undergoes oxidation to form a PE bond resulting in the formation of complexes of the type [Cu(kappa(2)-P,P'-DPEphos)(kappa(2)-P,E-DPEphos-E)][BF4] (2, E = O; 3, E = S; 4, E = Se) containing a Cu-E bond. The zigzag polymeric Cu-I complex [Cu(kappa(2)-P,P'-DPEphos)(mu-4,4'-bpy)](n)[BF4](n) (5) was …

Inorganic chemistryCu-I ComplexesBite AngleEtherEmitting Electrochemical-CellsBite angleMedicinal chemistryTransition-Metal ChemistryInorganic Chemistrychemistry.chemical_compounddifenyylifosfinoMoleculeReactivity (chemistry)Staudinger reactionPhysical and Theoretical ChemistryMonooxidized Bis(Phosphino)AminesMolecular-StructureStructural-CharacterizationDichloromethaneChemistryCationic polymerizationPlatinum(Ii) Complexeskupari(I) kompleksitWilliamson ether synthesisState Methodcopper(I) complexStaudinger ReactiondiphenylphosphinoInorganic Chemistry
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Potential anticancer heterometallic Fe-Au and Fe-Pd agents: Initial mechanistic insights

2013

A series of gold(III) and palladium(II) heterometallic complexes with new iminophosphorane ligands derived from ferrocenylphosphanes [{Cp-P(Ph2)═N-Ph}2Fe] (1), [{Cp-P(Ph2)═N-CH2-2-NC5H4}2Fe] (2), and [{Cp-P(Ph2)═N-CH2-2-NC5H4}Fe(Cp)] (3) have been synthesized and structurally characterized. Ligands 2 and 3 afford stable coordination complexes [AuCl2(3)]ClO4, [{AuCl2}2(2)](ClO4)2, [PdCl2(3)], and [{PdCl2}2(2)]. The complexes have been evaluated for their antiproliferative properties in human ovarian cancer cells sensitive and resistant to cisplatin (A2780S/R), in human breast cancer cells (MCF7) and in a nontumorigenic human embryonic kidney cell line (HEK-293T). The highly cytotoxic trimeta…

STRUCTURAL-CHARACTERIZATIONARENE-RUTHENIUM COMPLEXESStereochemistryANTITUMOR-ACTIVITYchemistry.chemical_elementGOLD COMPOUNDSAntineoplastic AgentsCYTOTOXIC ACTIVITYArticleCoordination ComplexesCell Line TumorDrug DiscoveryOrganometallic CompoundsmedicineHumansCytotoxic T cellFerrous CompoundsBIOLOGICAL-PROPERTIESGroup 2 organometallic chemistryCisplatinHEK 293 cellsIn vitroPLATINUM(II) COMPLEXESHEK293 CellschemistryCELL-DEATHCell cultureCancer cellMolecular MedicineMETAL-COMPLEXESCisplatinOrganogold CompoundsPalladiumX-RAY-STRUCTUREPalladiummedicine.drug
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Phenoxyamidine Zn and Al Complexes: Synthesis, Characterization, and Use in the Ring-Opening Polymerization of Lactide

2019

International audience; Herein we report the synthesis of new ditopic ligands, which consist of a phenoxy group and N,N,N'trisubstituted amidines linked by a methylene spacer (L1-L4). Their coordination chemistry has been studied/investigated with Zn(II) and Al(III). Alkane elimination route between the phenol-amidine proligands (L1H-L4H) and Et2Zn led to dinuclear complexes [(L1-L4)ZnEt]2 (1a-4a) in which the Zn centers are chelated by phenoxyamidine ligands and bridged through the oxygen atom of the phenoxy groups. Salt metathesis reaction between two equivalents of the sodium amidine phenate L1Na and ZnCl2 led to a bis-chelate chiral spiro-complex (L12Zn) 1a'. Analogous alkane eliminatio…

STRUCTURAL-CHARACTERIZATIONchemistry.chemical_elementCATALYSTSZinc010402 general chemistryLIGANDS SYNTHESIS01 natural sciencesRing-opening polymerizationCoordination complexCatalysisInorganic Chemistrychemistry.chemical_compoundZINCIMINE LIGANDSGroup (periodic table)Polymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMethyleneCYCLIC ESTERSALUMINUM COMPLEXESchemistry.chemical_classificationEPSILON-CAPROLACTONELactide010405 organic chemistryOrganic ChemistryGROUP-4 METAL-COMPLEXES[CHIM.CATA]Chemical Sciences/CatalysisImine ligands0104 chemical scienceschemistryINITIATORSGROUP-4 METAL-COMPLEXES; ALUMINUM COMPLEXES; EPSILON-CAPROLACTONE; LIGANDS SYNTHESIS; IMINE LIGANDS; STRUCTURAL-CHARACTERIZATION; CYCLIC ESTERS; ZINC; CATALYSTS; INITIATORS
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Electrochemistry of Bis(pyridine)cobalt (Nitrophenyl)corroles in Nonaqueous Media

2018

International audience; A series of bis(pyridine)cobalt corroles with one or three nitrophenyl groups on the meso positions of the corrole macrocycle were synthesized and characterized as to their electrochemical and spectroscopic properties in dichloromethane, benzonitrile, and pyridine. The potentials for each electrode reaction were measured by cyclic voltammetry and the electron-transfer mechanisms evaluated by analysis of the electrochemical data combined with UV-visible spectra of the neutral, electroreduced, and electroxidized forms of the corroles. The proposed electronic configurations of the initial compounds and the prevailing redox reactions involving the electroactive central c…

[SPI.OTHER]Engineering Sciences [physics]/Otherelectronic-structuremanganese corroleschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistryConjugated system010402 general chemistryElectrochemistry01 natural sciencesInorganic Chemistryporphyrin-corrole dyadschemistry.chemical_compoundcopper corroleswater-oxidationPyridinePolymer chemistryacid-media[CHIM]Chemical Sciencesaryl-substituted corrolesredox potentialsPhysical and Theoretical ChemistryCorrole010405 organic chemistry0104 chemical sciencesSolventBenzonitrilechemistrystructural-characterizationefficient synthesisCyclic voltammetryCobaltInorganic Chemistry
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