Search results for "Nation"

showing 10 items of 16428 documents

Palladium-catalyzed amination of aryl dibromides with secondary amines: synthetic and mechanistic aspects

1999

Abstract Diaminobenzenes are obtained starting from m- and p-dibromobenzenes and secondary amines in the presence of Pd(dba)2/P(o-tolyl)3and sodium tert-butoxide in moderate to good yields. Reductive dehalogenation of aryl dibromides is a major side reaction under these conditions. The study of this reaction has shown that the formation of reductive dehalogenation products occurs according to two independent ways. The first one proceeds via the well-known β-hydride elimination from amido-coordinated palladium complexes. The second one involves the formation of hydrido palladium complexes from amino-coordinated derivatives. Although our results do not allow us to propose a detailed mechanist…

010405 organic chemistryChemistryArylOrganic ChemistrySide reactionHalogenationchemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundDeprotonationDrug Discovery[CHIM]Chemical SciencesOrganic chemistryComputingMilieux_MISCELLANEOUSAminationPalladiumTetrahedron Letters
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Two bimetallic layered materials with “Cu4Fe3” defective cubane units: syntheses, structures and magnetic properties of {[CuII(tn)]2[FeII(CN)6]}3·[Na…

2005

Abstract Reactions of the [Fe III (CN) 6 ] 3− anion with the [Cu II (tn)] 2+ ion (tn = 1,3-diaminopropane) afford the compounds {[Cu II (tn)] 2 [Fe II (CN) 6 ]}3·[Na 3 Fe III (CN) 6 ]·12H 2 O (1) and {[Cu n (tn)] 2 [Fe II (CN) 6 ]}·KCl·5H 2 O (2). Despite the differences concerning their asymmetric units, both structures present strong similar features: in both structures, the Cu(II) ion presents a square-base pyramidal CuN 5 environment and each [Fe II (CN) 6 ] 4− anion is linked to six Cu(II) ions through its six N atoms leading to infinite [Cu II (tn)] 2 [Fe II (CN) 6 ] layers which can be viewed as 2-D layered arrangement generated by the defective cubane units Cu 4 Fe 3 involving Fe-CN…

010405 organic chemistryChemistryCoordination polymerMechanical EngineeringInorganic chemistryMetals and AlloysCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsParamagnetismchemistry.chemical_compoundCrystallographyTransition metalMechanics of MaterialsCubaneMaterials ChemistryMoleculeAntiferromagnetismBimetallic stripSynthetic Metals
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Spin crossover (SCO) iron(II) coordination polymer chain: Synthesis, structural and magnetic characterizations of [Fe(abpt)2(μ-M(CN)4)] (M=PtII and N…

2013

Abstract New iron(II) coordination polymeric neutral chain of formula [Fe(abpt) 2 (μ-M(CN) 4 )], with M = Pt II ( 1 ), Ni II ( 2 ) and abpt = 4-amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole, have been synthesized and characterized by infrared spectroscopy, X-ray diffraction and magnetic measurements. The two compounds are isostructural as deduced from a Rietveld analysis of X-ray powder diffraction data of 2 simulated from the single crystal structure of 1 . The crystal packing of 1 is formed by regular chains running along the crystallographic [−1 0 1] direction where the planar [Pt(CN) 4 ] 2− anion acts as a μ 2 -bridging ligand via two nitrogen atoms of two different trans cyano groups, whi…

010405 organic chemistryChemistryCoordination polymerRietveld refinementInorganic chemistryBridging ligand010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographySpin crossoverMaterials Chemistry[CHIM.CRIS]Chemical Sciences/CristallographyPhysical and Theoretical ChemistryIsostructuralSingle crystalPowder diffraction
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A versatile rigid binucleating ligand for Rh2(μ-Cl)2 moieties: its application as a catalyst in hydrogenation and cyclopropanation

2003

A rigid non-deforming "MCl 2 M" binucleating ligand [7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 ] - able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + . Hydrogenation of 1-hexene is 10 times faster with [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + than with [Rh 2 (C 5 Me 5 ) 2 Cl 4 ]. A hydrogenation mechanism has been proposed which assumes that [Rh 2 (C 5 Me 5 ) 2 (Cl)(H){7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + is the first generated species in the process.

010405 organic chemistryChemistryCyclopropanationStereochemistryOrganic Chemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryRhodium compounds0104 chemical sciencesCatalysisRhodiumInorganic ChemistryMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Exploring the Chemoselectivity towards Cysteine Arylation by Cyclometallated Au III Compounds: New Mechanistic Insights

2020

To gain more insight into the factors controlling the efficient cysteine arylation by cyclometalated Au(III) complexes, the reaction between selected gold compounds and different peptides was investigated by high‐resolution liquid chromatography electrospray ionization mass spectrometry (HR‐LC‐ESI‐MS). The deducted mechanisms of C–S cross‐coupling, also supported by density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations, evidenced the key role of secondary peptidic gold binding sites in favouring the process of reductive elimination.

010405 organic chemistryChemistryElectrospray ionizationOrganic Chemistrycyclometallated gold complexes010402 general chemistryMass spectrometry01 natural sciencesBiochemistryCombinatorial chemistryMolecular mechanicsReductive elimination0104 chemical sciencesddc:cysteine arylationGold CompoundschemoselectivitySettore CHIM/03 - Chimica Generale E InorganicapeptidesMolecular MedicineDensity functional theoryChemoselectivityMolecular BiologyCysteinemass spectrometry
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Photochemically Produced Singlet Oxygen: Applications and Perspectives

2018

This Review aims to provide early stage researchers with an updated guide to applications of photochemically produced singlet oxygen and, at the same time, widen the experienced researcher's perspectives in a holistic approach to singlet oxygen chemistry. Without being exhaustive, literature between 2010 and early 2018 has been surveyed by focusing on a critical evaluation of new knowledge and applications. After an introductory section concerning singlet oxygen production, detection, and interactions with biological systems, subsequent sections describe current applications of singlet-oxygen-enabled technology. Besides strictly chemical synthesis applications, attention has been given to t…

010405 organic chemistryChemistryEnvironmental remediationSinglet oxygenmedicine.medical_treatmentOrganic ChemistryPhotodynamic therapySettore CHIM/06 - Chimica Organica010402 general chemistryPhotochemistry01 natural sciencessinglet oxygen0104 chemical sciencesAnalytical Chemistryphotooxygenation reactionchemistry.chemical_compoundphotodynamic therapymedicinePhysical and Theoretical Chemistryenvironmental remediationphototherapy
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TiO2 Nanoparticles Functionalized with Non-innocent Ligands Allow Oxidative Photocyanation of Amines with Visible/Near-Infrared Photons

2018

Photosynthesis is an efficient mechanism for converting solar light energy into chemical energy. We report on a strategy for the aerobic photocyanation of tertiary amines with visible and near-infrared (NIR) light. Panchromatic sensitization was achieved by functionalizing TiO2 with a 2-methylisoquinolinium chromophore, which captures essential features of the extended π-system of 2,7-diazapyrenium (DAP2+) dications or graphitic carbon nitride. Two phenolic hydroxy groups make this ligand highly redox-active and allow for efficient surface binding and enhanced electron transfer to the TiO2 surface. Non-innocent ligands have energetically accessible levels that allow redox reactions to chang…

010405 organic chemistryChemistryGraphitic carbon nitrideGeneral ChemistryCyanationChromophore010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisNon-innocent ligand0104 chemical sciencesCatalysisElectron transferchemistry.chemical_compoundColloid and Surface ChemistryPhotocatalysisJournal of the American Chemical Society
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Photochemistry and Redox Chemistry of an Unsymmetrical Bimetallic Copper(I) Complex

2016

The bimetallic copper(I) complex Cu2L2 (cis-1) is formed with high diasteroselectivity from [Cu(NCCH3)4][BF4] and HL (4-tert-butyl phenyl(pyrrolato-2-yl-methylene)amine) in a kinetically controlled reaction. cis-1 features a rather short Cu···Cu distance of 2.4756(6) A and is weakly emissive at room temperature in solution. Oxidatively triggered disproportionation of cis-1 yields elemental copper and the mononuclear copper(II) complex CuL2 (trans-2). One-electron reduction of trans-2 gives cuprate [2]– with a bent bis(pyrrolato) coordinated copper(I) entity. The imine donor atoms of [2]– can insert an additional copper(I) ion giving exclusively the bimetallic complex cis-1 closing the oxida…

010405 organic chemistryChemistryIminechemistry.chemical_elementDisproportionation010402 general chemistryPhotochemistry01 natural sciencesRedoxCopper0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundAmine gas treatingCupratePhysical and Theoretical ChemistryBimetallic stripInorganic Chemistry
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Electrochemical, Spectroelectrochemical, and Structural Studies of Mono- and Diphosphorylated Zinc Porphyrins and Their Self-Assemblies

2019

International audience; Three series of porphyrins containing a Zn(II) central metal ion and zero, one or two phosphoryl groups at the meso-positions of the macrocycle were characterized as to their electrochemical, spectroscopic and structural properties in non-aqueous media. The investigated compounds are represented as 5,15-bis(4'-R-phenyl)porphyrinatozinc, 10-(diethoxyphosphoryl)-5,15-bis(4'-R-phenyl)porphyrinatozinc and 5,15-bis(diethoxyphosphoryl)-10,20-bis(4'-R-phenyl)porphyrinatozinc, where R = OMe, Me, H or CN. Linear-free energy relationships are observed between the measured redox potentials at room temperature and the electronic nature of the substituents at the 5 and 15 meso-ph…

010405 organic chemistryChemistryInorganic chemistrychemistry.chemical_elementZinc010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetal[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryvisual_artvisual_art.visual_art_medium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry
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An investigation of photo- and pressure-induced effects in a pair of isostructural two-dimensional spin-crossover framework materials

2014

International audience; Two new isostructural iron(II) spin-crossover (SCO) framework (SCOF) materials of the type [Fe(dpms)2 (NCX)2 ] (dpms=4,4'-dipyridylmethyl sulfide; X=S (SCOF-6(S)), X=Se (SCOF-6(Se))) have been synthesized. The 2D framework materials consist of undulating and interpenetrated rhomboid (4,4) nets. SCOF-6(S) displays an incomplete SCO transition with only approximately 30 % conversion of high-spin (HS) to low-spin iron(II) sites over the temperature range 300-4 K (T1/2 =75 K). In contrast, the NCSe(-) analogue, SCOF-6(Se), displays a complete SCO transition (T1/2 =135 K). Photomagnetic characterizations reveal quantitative light- induced excited spin-state trapping (LIES…

010405 organic chemistryChemistryIronOrganic ChemistrySpin transitionMineralogyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryAtmospheric temperature range010402 general chemistrySpin crossover01 natural sciencesCatalysisLIESST0104 chemical sciencesCoordination polymersChalcogenCrystallographySpin crossoverExcited stateMetastabilityMagnetic propertiesChalcogensIsostructural
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