Search results for "AGN"

showing 10 items of 28126 documents

Organotin(IV) derivatives containing heteroditopic pyridyl-quinolin-8-olate ligands: Synthesis and structures

2021

Abstract Six novel neutral organotin(IV) complexes, viz. [n-Bu2Sn(L4-PyAQ)2] 1, [Bz2Sn(L4-PyAQ)2] 2, [Ph2Sn(L4-PyAQ)2] 3, [Ph2Sn(L3-PyAQ)2] 4, [Bz3Sn(L4-PyAQ)] 5 and [Ph3Sn(L4-PyAQ)] 6 have been synthesized via reactions of 3/4-pyridyl-quinolin-8-ol pro-ligands, with appropriate diorganotin oxide and triorganotin hydroxide precursors, respectively. The compounds 1-6 were characterized in solution by means of NMR spectroscopy while the solid-state structures of 1, 6, and of the solvates 2·1.5C6H6, 3·0.25C6H6, 2·4·C6H6, and 5·0.5H2O were authenticated by single crystal X-ray diffraction analysis. In the solid-state, the tin centers in 1-2·4·C6H6 are hexacoordinated and reveal a distorted cis-…

010405 organic chemistryChemistryOrganic ChemistryOxidechemistry.chemical_elementNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesBiochemistrySquare pyramidal molecular geometry0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundMaterials ChemistryHydroxidePhysical and Theoretical ChemistryTinSingle crystalJournal of Organometallic Chemistry
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Interactions of a Diplumbyne with Dinuclear Transition Metal Carbonyls to Afford Metalloplumbylenes

2020

The metathesis reactions of the diplumbyne AriPr6PbPbAriPr6 (AriPr6 = −C6H3–2,6-(C6H2–2,4,6-iPr3)2) with the dinuclear metal carbonyls Mn2(CO)10, Fe2(CO)9, and Co2(CO)8 under mild conditions afforded the complexes Mn(CO)5(PbAriPr6) (1), Fe(CO)4(PbAriPr6)2 (2), and Co4(CO)9(PbAriPr6)2 (3), respectively. Complexes 1–3 were structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by 1H, 13C{1H}, 59Co{1H}, and 207Pb{1H} NMR; UV–vis; and IR methods. They are rare examples of species formed by the direct reaction of a group 14 dimetallyne with transition metal carbonyls. Complexes 1 and 2 feature Mn–Pb or Fe–Pb single bonds, whereas in 3 a Co–Pb cluster i…

010405 organic chemistryChemistryOrganic ChemistrycarbonylsmetalsMetal carbonylkompleksiyhdisteetorganometalliyhdisteet010402 general chemistry01 natural sciencescobalttransition metals0104 chemical sciencesInorganic ChemistryTransition metalPolymer chemistrySalt metathesis reactionPhysical and Theoretical Chemistrykarbonyylitnuclear magnetic resonance spectroscopy
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Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine

2017

A p-tert-butylphenyl substituted 4H-dithieno[2,3-b:3′,2′-e][1,4]thiazine was synthesized by twofold Buchwald–Hartwig coupling. The electronic properties (UV/Vis, cyclic voltammetry and spectroelectrochemistry) and the DFT- and TD DFT-calculated electronic structure reveal that the parent system and the radical cation and dication oxidation products are highly polarizable π-systems with strong charge transfer contributions. The radical cation and the dication were prepared by oxidation with antimony(V) pentachloride, giving stable deeply colored salts. EPR spectroscopy of the radical cation furnishes hyperfine coupling constants with the nitrogen nucleus and the α-thienyl protons. The dicati…

010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_elementElectronic structureNuclear magnetic resonance spectroscopy010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionDicationchemistry.chemical_compoundRadical ionAntimonyThiazinelawCyclic voltammetryElectron paramagnetic resonanceOrganic Chemistry Frontiers
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Exploring the Slow Relaxation of the Magnetization in CoIII -Decorated {DyIII 2 } Units

2016

We have prepared and structurally characterized a new member of the butterfly-like {CoIII 2DyIII 2} single-molecule magnets (SMMs) through further CoIIIdecoration, with the formula [CoIII 4DyIII 2(OH)2(teaH)2(tea)2(Piv)6] (teaH3=triethanolamine; Piv=trimethylacetate or pivalate). Direct current (DC) susceptibility and magnetization measurements were performed allowing the extraction of possible crystal-field parameters. A simple electrostatic modeling shows reasonable agreement with experimental data. Alternating current (AC) susceptibility measurements under a zero DC field and under small applied fields were performed at different frequencies (i.e., 10–1500 Hz) and at low temperatures (i.…

010405 organic chemistryChemistryOtras Ciencias QuímicasOrganic ChemistryCiencias QuímicasAnalytical chemistryGeneral ChemistryCOORDINATION COMPLEXLANTHANIDESMAGNETIC PROPERTIES010402 general chemistry01 natural sciencesSINGLE-MOLECULE MAGNETSCatalysisDYSPROSIUM0104 chemical sciencesMagnetizationRelaxation (physics)Physical chemistryCIENCIAS NATURALES Y EXACTASChemistry - A European Journal
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A rare polymeric azido-bridged copper(II) chain with a pentameric repeating unit: Synthesis, structure and magnetic properties

2013

International audience; The novel polymeric chain copper(II) complex [Cu4(μ-Mesalpn)2(μ1,1,1-N3)2(μ1,1-N3)2Cu]n (1) was prepared by the reaction of Cu(NO3)2·3H2O with Mesalpn in the presence of an excess of NaN3. A single-crystal X-ray diffraction study showed an unusual 1D polymeric chain based on pentanuclear Cu5 units with both μ1,1,1-N3 and μ1,1-N3 bridges, and with three independent Cu(II) ions presenting three different coordination numbers (4, 5 and 6). The magnetic susceptibility data show the presence of dominant anti-ferromagnetic interactions.

010405 organic chemistryChemistryPentanuclearCoordination numberchemistry.chemical_elementSingle-crystal010402 general chemistry01 natural sciencesMagnetic susceptibilityCopper0104 chemical sciences3. Good healthIonInorganic ChemistryCrystallographyChain (algebraic topology)Copper(II) complexMaterials Chemistry[CHIM]Chemical Sciences1D polymeric chainPhysical and Theoretical ChemistrySingle crystal
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Formation of dibutyl carbonate and butylcarbamate via CO2 insertion in titanium(IV) butoxide and reaction with n-butylamine

2016

Abstract The species resulting from insertion of 12CO2 and 13CO2 into titanium(IV) butoxide is for the first time fully characterized by means of infrared and nuclear magnetic resonance spectroscopy. Results show formation of Ti-monobutylcarbonate, that easily undergoes nucleophilic attack by an aliphatic amine. The hydrolysis of the resulting species produces butylcarbamate and dibutylcarbonate as the only main products. Characterization results of the carbonate-like adduct, along with its reactivity with amine molecules open the route to new ways of CO2 utilization as building block for valuable organic compounds.

010405 organic chemistryChemistryProcess Chemistry and Technologyn-Butylaminechemistry.chemical_elementNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesAdductHydrolysischemistry.chemical_compoundNucleophilePolymer chemistryChemical Engineering (miscellaneous)Organic chemistryReactivity (chemistry)Amine gas treatingSettore CHIM/07 - Fondamenti Chimici Delle TecnologieWaste Management and DisposalTitaniumDibutyl carbonate CO2 insertion Titanium alkoxides Carbamate
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Probing the guest-binding preference of three structurally similar and conformationally adaptive macrocycles.

2019

A hybrid macrocycle was synthesized by combining the repeat units in oxatub[4]arene and zorb[4]arene, and its recognition behavior and conformational analysis were studied. Three structurally similar and conformationally adaptive macrocycles show different guest-binding selectivities and preferences even in a complex mixture containing three macrocycles and three guests.

010405 organic chemistryChemistryStereochemistryMetals and AlloysGeneral Chemistry010402 general chemistry01 natural sciencesCatalysisPreference0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Conformational Switching of Multi-Responsive Ferrocenyl-Phenol Conjugates

2016

Multifunctional conformational switches based on the ferrocenyl-salicylic acid amide motif with increasing additional complexity at the Fc moiety (R = COOMe, CONHEt, CONHFc; H-2–H-4; Fc = ferrocenyl) have been prepared and their preferred secondary structures in solution have been elucidated by NMR and IR spectroscopy in combination with conformational searches based on DFT calculations. Their distinct conformational responses to deprotonation ([2]––[4]–) and oxidation ([H-2]+·–[H-4]+·) have been revealed by IR, EPR, and UV/Vis spectroscopy as well as by DFT calculations. Deprotonation inverts all amide units (double amide twist) whereas oxidation selectively flips the terminal amide unit (…

010405 organic chemistryChemistryStereochemistryOrganic ChemistryInfrared spectroscopy010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundDeprotonationlawAmideMoietyPhenolPhenolsPhysical and Theoretical ChemistryElectron paramagnetic resonanceSpectroscopyEuropean Journal of Organic Chemistry
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Diferratricarbaboranes of thesubcloso-[(η5-C5H5)2Fe2C3B8H11] Type, the First Representatives of the 13-Vertex Dimetallatricarbaborane Series

2003

Treatment of the [2-Cp-9-tBuNH-closo-2,1,7,9-FeC 3 B 8 H 1 0 ] (1) ferratricarbollide (Cp = η 5 -C 5 H 5 -) with Na + C 1 0 H 8 - in 1,2-dimethoxyethane (DME) at room temperature produced an air-sensitive transient anion with a tentatively identified nido-[tBUNH-CpFeC 3 B 8 H 1 0 ] 2 - constitution. In-situ reaction of this low-stability ion with [CpFe(CO) 2 I] or [CpFe(CO) 2 ] 2 generated three violet diferratricarbaboranes identified as paramagnetic subcloso complexes [4,5-Cp 2 - -4,5,1,6,7-Fe 2 C 3 B 8 H 1 1 ] (2; yield 2%), [4,5-Cp 2 - -4,5,1,7,12-Fe 2 C 3 B 8 H 1 1 ] (3; yield 2%), and [7-tBuNH-4,5-Cp 2 - -4,5,1,7,12-Fe 2 C 3 B 8 H 1 0 ] (4; yield 14%). These first representatives of t…

010405 organic chemistryChemistryStereochemistryOrganic ChemistryInfrared spectroscopyBoranesGeneral Chemistry010402 general chemistryMass spectrometry01 natural sciencesCatalysis3. Good health0104 chemical sciencesIonlaw.inventionVertex (geometry)CrystallographyParamagnetismlawYield (chemistry)Electron paramagnetic resonanceChemistry - A European Journal
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A hybrid magnet with coexistence of ferromagnetism and photoinduced Fe(iii) spin-crossover

2011

International audience; The insertion of a [Fe(sal2-trien)]+ complex cation into a 2D oxalate network results in a hybrid magnet with coexistence of magnetic ordering and photoinduced spin-crossover (LIESST effect) in compound [FeIII(sal2-trien)][MnIICrIII(ox)3]*(CH2Cl2) (1). A complete photomagnetic characterization together with a detailed structural analysis of the low-spin (LS) and high-spin (HS) structures of 1 is presented in order to understand such unusual behavior. This very rare and unexpected property in a FeIII spin-crossover complex, has been attributed to the strong distortion exhibited by the metastable HS state. Furthermore, 1 has shown that, in contrast to what has been pre…

010405 organic chemistryChemistryStereochemistry[CHIM.MATE]Chemical Sciences/Material chemistryGeneral Chemistry010402 general chemistry01 natural sciencesLIESSTOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographyFerromagnetismSpin crossoverMetastabilityMagnetSpin (physics)Chemical Science
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