Search results for "Pyridine ligands"

showing 5 items of 5 documents

Synthesis and photophysical properties of dansyl-based polyamine ligands and their Zn(II) complexes

2007

The synthesis, potentiometric studies and photophysical properties of two new polyamine ligands (L1 and L2) possessing the dansyl chromophore were studied in aqueous 0.15 M NaCl. The compounds show the absorption and emissions bands characteristic of the dansylamide fluorophore and both present intramolecular excited state proton transfer at intermediate pH ranges. One of the ligands (L2) strongly coordinates Zn(II) leading to fluorescence quenching. A model compound (L3) of the dansyl moiety was also investigated. http://www.sciencedirect.com/science/article/B6TG5-4MB4DV1-2/1/45cafbcee9a8df7daddd765512437ca3

ChemosensorsFluorophoreAqueous solutionPyridine ligands010405 organic chemistryChemistryPotentiometric titrationChromophore010402 general chemistryPhotochemistry01 natural sciencesFluorescenceFluorescence3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundIntramolecular forceMaterials ChemistryMoietyPhysical and Theoretical ChemistryPolyamineZn(II) complexesPolyamine ligandsInorganica Chimica Acta
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Nickel precursors based on diamagnetic and paramagnetic di(imine)pyridine ligands for magnetic materials: Synthesis, X-ray structures and magnetic st…

2018

International audience; Structural characterization and spectroscopic studies of the (2-acetyl-6-(1-TEMPO-imino)ethyl)pyridine (pat) and the 2,6-bis(1-TEMPO-imino)ethyl)pyridine (pbtMe) ligands are presented. Their electrochemical properties are also discussed. Two new nickel complexes, [NiII(dip)(CH3CN)(H2O)2](BF4)2 (1) (dip = 2,6-(di-iminepyridine)) and [NiII(pbtMe)(CH3CN)3](BF4)2 (2) have been characterized by X-ray diffraction. The reaction of 1 with the tetraethyl ammonium pentacyanopropenide salt (Et4N)(pcp) affords the new compound [NiII(pcp)(dip)(CH3CN)](pcp) (3) for which X-ray diffraction studies evidence an usual bridging μ2 coordination mode for the pentacyanopropenide anion, le…

Iminechemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciencesIonInorganic ChemistryParamagnetismchemistry.chemical_compoundMagnetic interactions[CHIM.ANAL]Chemical Sciences/Analytical chemistryPyridineMaterials ChemistryAntiferromagnetism[CHIM]Chemical SciencesCoordination polymerPhysical and Theoretical ChemistryNickel complexes010405 organic chemistryChemistry[CHIM.MATE]Chemical Sciences/Material chemistryDi(imine)pyridine ligands0104 chemical sciencesNickelCrystallographyDiamagnetism
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Synthesis and application of new iminopyridine ligands in the enantioselective palladium-catalyzed allylic alkylation

2014

A variety of iminopyridines were obtained by condensation of chiral amines with pyridine-2-carboxaldehyde and quinoline-8-carbaldehyde, or of aminoalkylpyridine derivatives with chiral ketones. These ligands were assessed in the enantioselective palladium catalyzed allylic substitution of 1,3-diphenylprop-2-enyl acetate with dimethyl malonate affording the product dimethyl 1,3-diphenylprop-2-enylmalonate in good yields and moderate enantioselectivities (up to 62% ee). Catalytic activity and enantioselectivity were found to be highly dependent upon the steric properties of the ligands. The best enantioselectivity (62% ee) was obtained by an iminopyridine based on a camphane skeleton. © 2014 …

Steric effectsAllylic rearrangementChemistryProcess Chemistry and TechnologyIminopyridine ligandsEnantioselective synthesischemistry.chemical_elementQuímicaDimethyl malonateMedicinal chemistryAllylic substitutionPalladium catalysisCatalysisCatalysischemistry.chemical_compoundTsuji–Trost reactionOrganic chemistryEnantioselective catalysisPhysical and Theoretical ChemistryPalladium
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Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes

2021

Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes. Financial support from the Deutsche Forschungsge-meinschaft [DFG, Priority Program SPP 2102] "Light-controlled reactivity of metal complexes" (BA 4467/7-1, LO 714/11-1, …

TrisDenticitysynthesisPyridinepyridine derivativecarbenoidIron compoundsCatalysisexperimental studychemistry.chemical_compoundPyridineMaterials Chemistryphysical chemistrycontrolled studyChemistrySinglet oxygenPyridine ligandsSinglet oxygenMetals and AlloysMesoionicGeneral ChemistryNanosecondPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsunclassified drugCrystallographyPhotophysicsiron complexisomerCeramics and CompositesCarbeneschemical structurephotodynamicsphysicsExcitationchemical parameters
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Transition metal ion induced hydrogelation by amino-terpyridine ligands

2014

Hydrogelation behavior of two amino-terpyridine ligands in the presence of divalent metal ions in water was studied in detail. The effect of ligand structure and different counter anions on the gel morphologies was also explored. peerReviewed

hydrogelationamino-terpyridine ligandstransition metal ion
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