Search results for "nm"

showing 10 items of 34737 documents

Cis- and trans molybdenum oxo complexes of a prochiral tetradentate aminophenolate ligand : Synthesis, characterization and oxotransfer activity

2020

Abstract Reaction of [MoO2Cl2(dmso)2] with the tetradentate O2N2 donor ligand papy [H2papy = N-(2-hydroxybenzyl)-N-(2-picolyl)glycine] leads to formation of the dioxomolybdenum(VI) complex [MoO2(papy)] (1) as a mixture of cis and trans isomers. Recrystallization from methanol furnishes solid cis-1, whereas the use of a dichloromethane-hexane mixture allows for the isolation of the trans-1 isomer. Both isomers have been structurally characterized by X-ray crystallography and the energy difference between the isomeric pair has been investigated by electronic structure calculations. Optimization of two configurational isomers in the gas phase predicts the trans isomer to lie 2.5 kcal/mol lower…

010405 organic chemistryChemistrycomputational modellingStereoisomerism010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistrySolventvariable temperature NMRTripodal ligandepoxidationMaterials ChemistryTheoretical chemistryProton NMRtripodal ligandPhysical and Theoretical ChemistryIsomerizationOxo Atom TransferCis–trans isomerism
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New crystal structures of fluorinated α-aminophosphonic acid analogues of phenylglycine

2020

The four novel phosphonic acid analogues of phenylglycine with various substituents in phenyl ring (mostly fluorine atoms) have been synthesized by using procedure of amidoalkylation of phosphorus trichloride with aromatic aldehydes and acetamide. The NMR, ESI-MS spectroscopy, and single-crystal X-Ray diffraction methods were used to characterize unusual structures: the amino-(4-trifluoromethylbenzyl)-(1), amino-(3,4-difluorobenzyl)-(2), amino-(2,4,6-trifluorobenzyl)-(3), and amino-(2-fluoro-4-hydroxybenzyl)-(4) phosphonic acids. Since the α-aminophosphonates have a potential for biological activity and could be used as building blocks in medicinal chemistry, it is important to know their d…

010405 organic chemistryCrystal and molecular structureschemistry.chemical_elementBiological activityCrystal structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciencesMedicinal chemistryNMRESI-MS spectra0104 chemical sciencesTurn (biochemistry)chemistry.chemical_compoundchemistryFluorinated α-aminophosphonic acidFluorinePhosphorus trichloridePhysical and Theoretical ChemistrySpectroscopyAcetamideStructural Chemistry
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Strecker reactions with hexacyanoferrates as non-toxic cyanide sources

2019

The Strecker reaction is the most widely applied three-component reaction. Although highly useful for the preparation of α-amino nitriles, α-amino acids, hydantoins and numerous related compounds, the need for the application of toxic sources of HCN limits its application in both academic and industrial settings. Here, we present a facile protocol for Strecker reactions using a mixture of potassium ferri- and ferrocyanides as a non-toxic substitute.

010405 organic chemistryCyanidePotassiumStrecker amino acid synthesischemistry.chemical_element010402 general chemistry01 natural sciencesPollution0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental ChemistryOrganic chemistryFerrocyanideGreen Chemistry
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Hierarchical Beta zeolites as catalysts in a one-pot three-component cascade Prins–Friedel–Crafts reaction

2020

Hierarchical Beta zeolites obtained from concentrated reaction mixtures (H2O/Si = 2.5–7.0) in the presence of CTAB and their conventional and nanosponge analogues were investigated in a one-pot cascade environmentally friendly Prins–Friedel–Crafts reaction of butyraldehyde with 3-buten-1-ol and anisole under mild conditions (60 °C). The highest yields of the desired products with 4-aryltetrahydropyran structure were achieved when using hierarchical zeolites characterised by well-developed mesoporosity (facilitating the formation of bulky intermediates and products) and by an increased fraction of highly accessible (evaluated by TTBPy method) medium-strength Bronsted acid sites. Acid sites w…

010405 organic chemistryEther010402 general chemistryAnisole01 natural sciencesPollutionEnvironmentally friendly0104 chemical sciencesCatalysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistryEnvironmental ChemistryOrganic chemistryButyraldehydeBrønsted–Lowry acid–base theoryFriedel–Crafts reactionComputingMilieux_MISCELLANEOUSGreen Chemistry
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2-Methyltetrahydrofuran: A Green Solvent for Iron-Catalyzed Cross-Coupling Reactions

2018

Iron‐catalyzed cross‐coupling reactions allow sustainable formation of C−C bonds using cost‐effective, earth‐abundant base‐metal catalysis for complex syntheses of pharmaceuticals, natural products, and fine chemicals. The major challenge to maintain full sustainability of the process is the identification of green and renewable solvents that can be harnessed to replace the conventional solvents for this highly attractive reaction. Herein, iron‐catalyzed cross‐coupling of aryl chlorides and tosylates with challenging organometallic reagents possessing β‐hydrogens is found to proceed in good to excellent yields with the green, sustainable, and eco‐friendly 2‐methyltetrahydrofuran (2‐MeTHF) a…

010405 organic chemistryGeneral Chemical EngineeringAryl2-MethyltetrahydrofuranHomogeneous catalysis010402 general chemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesCatalysisSolventchemistry.chemical_compoundGeneral EnergychemistryReagentFunctional groupEnvironmental ChemistryGeneral Materials ScienceChemSusChem
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Protonation of a Spherical Macrotricyclic Tetramine: Water Inclusion, Allosteric Effect, and Cooperativity

2017

The spherical macrotricyclic cryptand tetramine "C24" (1) displays remarkable protonation behaviour. It undergoes protonation in four successive steps for which pKa values of 11.17±0.05, 10.28±0.04, 6.00±0.06 and 3.08±0.08 have been determined at 298 K. The unusually close values for the first two protonations provide evidence for the encapsulation of a water molecule serving as effector for the second protonation, which is consistent with earlier observations that the exchange of protons bound in the diprotonated species with solvent protons is unusually slow and that 17 O NMR spectra show the presence of an oxygen centre in the same species quite distinct from that of solvent water. Encap…

010405 organic chemistryHydrogen bondprotonationPicrateCryptandProtonationCooperativityGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesSolventNMR spectra databasechemistry.chemical_compoundCrystallographymacrocycleschemistrysupramolekulaarinen kemiaMoleculeta116tetraminesChemPlusChem
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Hexanuclear manganese(III) single-molecule magnets based on oxime and azole-type ligands

2019

Abstract Two novel hexanuclear manganese(III) complexes belonging to the Mn6 family of single-molecule magnets (SMMs), of formulae [Mn6(μ3-O)2(H2N-sao)6(bta)2(EtOH)6]·2EtOH·4H2O (1) and [Mn6(μ3-O)2(H2N-sao)6(pta)2(EtOH)6]·4EtOH (2) [H2N-saoH2 = salicylamidoxime, bta = 1,2,3-benzotriazolate anion, pta = 5-phenyl-tetrazolate anion], have been synthesized and characterized structurally and magnetically. Both compounds crystallize in the triclinic system with space group P 1 ¯ (1 and 2). In their crystal packing, adjacent Mn6 complexes are connected through non-coordinating solvent molecules, which are H-bonded to N atoms of azole rings and –NH2 groups of salicylamidoxime ligand. The study of t…

010405 organic chemistryLigandMetal ions in aqueous solutionRelaxation (NMR)chemistry.chemical_elementManganeseTriclinic crystal system010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographyMagnetizationchemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryPolyhedron
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Highly Stable Neutral and Positively Charged Dicarbollide Sandwich Complexes

2005

Novel sandwich metallacarboranes commo-[3,3'-Ni(8-SMe2-1,2-C2B9H10)2] (1), commo-[3,3'-Co(8-SMe2-1,2-C2B9H10)2]+ (2+), commo-[3,3'-Ru(8-SMe2-1,2-C2B9H10)2] (4) and commo-[3,3'-Fe(8-SMe2-1,2-C2B9H10)2] (5) have been prepared by reaction of [10-SMe2-7,8-nido-C2B9H10]- with NiCl2 x 6 H2O, CoCl2, [RuCl2(dmso)4] and [FeCl2(dppe)], respectively. Reduction of 2+ with metallic Zn leads to the neutral and isolable complex commo-[3,3'-Co(8-SMe2-1,2-C2B9H10)2] (3). Theoretical calculations using the ZINDO/1 semiempirical method show three energy minima for complexes 1-3 and 5 that agree with the presence of three different rotamers in solution at low temperature, while four relative energy minima have…

010405 organic chemistryLigandOrganic ChemistryGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesMetalNMR spectra databasechemistry.chemical_compoundCrystallographyFerrocenechemistryComputational chemistryvisual_artvisual_art.visual_art_mediumMoleculeZINDOConformational isomerismChemistry - A European Journal
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Design of bimetallic magnetic chains based on oxalate complexes: towards single chain magnets

2009

We describe the synthesis, structure and magnetic characterization of several oxalate-based bimetallic 1D systems. We will exemplify how by suitable choice of the molecular building blocks and strict control of their arrangement in the solid state, the magnetic properties of these low-dimensional materials can be tuned to finally obtain bimetallic oxalate chains behaving as single-chain magnets (SCM). First, we will focus on compounds [K(18-crown-6)][MII(bpy)Cr(ox)3] (1, 2; MII = Mn, Co; bpy = C10N2H8). The MnCr derivative behaves as a 1D ferromagnet down to 2 K, the lowest investigated temperature. The lack of magnetic ordering in this chain prompted us to prepare the more anisotropic MnCo…

010405 organic chemistryLigandRelaxation (NMR)Supramolecular chemistryGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryFerromagnetismMagnetGeneral Materials ScienceBimetallic stripDerivative (chemistry)CrystEngComm
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Oxygen Transfer from Trimethylamine N ‐Oxide to Cu I Complexes Supported by Pentanitrogen Ligands

2020

[N,N-bis(1-methyl-2-benzimidazolyl)methyl-N-(bis-2-pyridylmethyl)amine] (L1) and [N,N-bis(2-quinolylmethyl)-N-bis(2-pyridyl)methylamine] (L2) were employed to prepare CuII and CuI complexes for spectroscopic and structural characterization. [L1CuII(H2O)](NO3)2 and [L2CuII(NO3)]NO3 have Jahn–Teller distorted octahedral geometries and give rise to isotropic EPR spectra in frozen solution. [L1CuI(CH3CN)]OTf and [L2CuI(CH3CN)]OTf have distorted trigonal bipyramidal and tetrahedral solid-state structures, respectively. The N-donors display labile behavior in solution, based on variable-temperature 1H NMR studies. Addition of trimethylamine N-oxide (Me3NO) to solutions of [L1CuI(CH3CN)]OTf and [L…

010405 organic chemistryMethylamineTrimethylamine010402 general chemistry01 natural sciences0104 chemical sciencesAdductlaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistryOctahedronlawProton NMRElectron paramagnetic resonanceAcetonitrileEuropean Journal of Inorganic Chemistry
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