Search results for "Spectroscopy"

showing 10 items of 10293 documents

The Taming of Redox‐Labile Phosphidotitanocene Cations

2019

International audience; Tame d0 phosphidotitanocene cations stabilized with a pendant tertiary phosphane arm are reported. These compounds were obtained by one-electron oxidation of d1 precursors with [Cp2Fe][BPh4]. The electronic structure of these compounds was studied experimentally (EPR, UV/Vis, and NMR spectroscopy, X-ray diffraction analysis) and through DFT calculations. The theoretical analysis of the bonding situation by using the electron localization function (ELF) shows the presence of π-interactions between the phosphido ligand and Ti in the d0 complexes, whereas dπ–pπ repulsion prevents such interactions in the d1 complexes. In addition, CH–π interactions were observed in seve…

010402 general chemistry01 natural sciencesRedoxTransition metal phosphidesCatalysisFrustrated Lewis pairlaw.inventionchemistry.chemical_compoundFrustrated Lewis Pair (FLP)[CHIM.ANAL]Chemical Sciences/Analytical chemistrylaw[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphorus LigandsElectron paramagnetic resonanceDiphenylacetyleneComputingMilieux_MISCELLANEOUSTitanium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandOrganic Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyElectron localization function0104 chemical sciencesHomolysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryDensity Functional Theory (DFT)Crystallographychemistry[CHIM.CHEM]Chemical Sciences/CheminformaticsChemistry – A European Journal
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Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support

2020

Abstract Controlling the size and uniformity of metal clusters with atomic precision is essential for fine‐tuning their catalytic properties, however for clusters deposited on supports, such control is challenging. Here, by combining X‐ray absorption spectroscopy and density functional theory calculations, it is shown that supports play a crucial role in the evolution of monolayer‐protected clusters into catalysts. Based on the acidic nature of the support, cluster‐support interactions lead either to fragmentation of the cluster into isolated Au–ligand species or ligand‐free metallic Au0 clusters. On Lewis acidic supports that bind metals strongly, the latter transformation occurs while pre…

010402 general chemistry01 natural sciencesgold clustersNanomaterials | Hot PaperCatalysiskultaCatalysisNanomaterialsmonolayer-protected clustersMetalklusteritnoncovalent interactionskatalyytitMonolayerCluster (physics)Non-covalent interactionschemistry.chemical_classificationX-ray absorption spectroscopyFull Paper010405 organic chemistryOrganic ChemistryX-ray absorption spectroscopyGeneral ChemistryFull Papersgold0104 chemical sciencesX-Ray Absorption SpectroscopychemistryChemical physicsvisual_artdensity functional calculationsvisual_art.visual_art_mediumDensity functional theorynanohiukkasetcluster-support interactionChemistry (Weinheim an Der Bergstrasse, Germany)
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Unveiling the Occurrence of Co(III) in NiCo Layered Electroactive Hydroxides: The Role of Distorted Environments

2020

Co- and Ni-based layered hydroxides constitute a unique class of two-dimensional inorganic materials with exceptional chemical diversity, physicochemical properties and outstanding performance as supercapacitors and overall water splitting catalysts. Recently, the occurrence of Co(III) in these phases has been proposed as a key factor that enhance their electrochemical performance. However, the origin of this centers and control over its contents remains as an open question. We employed the Epoxide Route to synthesize a whole set of α-NiCo layered hydroxides. The PXRD and XAS characterization alert about the occurrence of Co(III) as a consequence of the increment in the Ni content. DFT+U si…

010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysisCatalysis//purl.org/becyt/ford/1 [https]symbols.namesake//purl.org/becyt/ford/1.4 [https]LAYERED HYDROXIDESX-ray absorption spectroscopy2D MATERIALS010405 organic chemistryChemistryOrganic ChemistryFermi levelGeneral Chemistry0104 chemical sciencesCharacterization (materials science)Chemical engineeringOctahedronWATER SPLITTINGsymbolsWater splittingENERGY STORAGESUPERCAPACITANCEChemistry – A European Journal
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Phosphasalen group IV metal complexes: synthesis, characterization and ring opening polymerization of lactide.

2020

International audience; We report the synthesis of a series of Zr and Ti complexes bearing phosphasalen which differs from salen by the incorporation of two P atoms in the ligand backbone. The reaction of phosphasalen proligands (1a-1c)H2 with Zr(CH2Ph)4 led to different products depending on the nature of the N,N-linker in the ligand. In case of ethylene-linked phosphasalen, octahedral Zr complex 2a formed as a single stereoisomer in trans geometry. With the phenylene linker, it was shown by dynamic NMR spectroscopy that complex 2b exists as a mixture of trans and cis-β isomers in solution, both enantiomers (Δ and Λ) of the cis-β isomer being in fast equilibrium with respect to the NMR tim…

010402 general chemistryLIGANDS SYNTHESIS01 natural sciencesRing-opening polymerizationCoordination complexInorganic ChemistryINDIUM COMPLEXESOctahedral molecular geometry[CHIM]Chemical SciencesSALALEN COMPLEXESCYCLIC ESTERSCOORDINATION CHEMISTRYZIRCONIUM COMPLEXES; COORDINATION CHEMISTRY; SALALEN COMPLEXES; LIGANDS SYNTHESIS; INDIUM COMPLEXES; SALEN LIGANDS; CYCLIC ESTERS; INITIATORS; CATALYSIS; ALUMINUMchemistry.chemical_classification010405 organic chemistryLigandCATALYSISCationic polymerizationNuclear magnetic resonance spectroscopyALUMINUM0104 chemical sciencesCrystallographychemistrySALEN LIGANDSAlkoxy groupINITIATORS[CHIM.OTHE]Chemical Sciences/OtherIsomerizationZIRCONIUM COMPLEXESDalton transactions (Cambridge, England : 2003)
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High-resolution rovibrational spectroscopy of c-C3H2+: The ν7 C–H antisymmetric stretching band

2020

Abstract The ν 7 antisymmetric C–H stretching fundamental of c- C 3 H 2 + has been characterized in a cryogenic 22-pole ion trap by a novel type of action spectroscopy, in which the rovibrational excitation of c- C 3 H 2 + is detected as a slowing down of the low-temperature reaction c- C 3 H 2 +  + H2 → C 3 H 3 + + H. Ninety-one rovibrational transitions with partly resolved fine structure doublets were measured in high resolution. Supported by high-level quantum chemical calculations, spectroscopic parameters were determined by fitting the observed lines with an effective Hamiltonian for an asymmetric rotor in a doublet electronic ground state, X ˜ A 1 2 , yielding a band origin at 3113.6…

010405 organic chemistryAntisymmetric relationChemistryOrganic ChemistryRotational–vibrational spectroscopy010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciencesAnalytical ChemistryInorganic Chemistrysymbols.namesakesymbolsMoleculeIon trapGround stateHamiltonian (quantum mechanics)SpectroscopySpectroscopyExcitationJournal of Molecular Structure
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Tuning the Electronic Properties of Nonplanar exTTF-Based Push–Pull Chromophores by Aryl Substitution

2012

International audience; A new family ofπ-extended tetrathiafulvalene (exTTF) donor−acceptorchromophores has been synthesized by [2 + 2] cycloaddition of TCNE with exTTF-substituted alkynes and subsequent cycloreversion. X-ray data and theoretical calculations,performed at the B3LYP/6-31G**level, show that the new chromophores exhibit highlydistorted nonplanar molecular structures with largely twisted 1,1,4,4-tetracyanobuta-1,3-diene (TCBD) units. The electronic and optical properties, investigated by UV/visspectroscopy and electrochemical measurements, are significantly modified when theTCBD acceptor unit is substituted with a donor phenyl group, which increases the twistingof the TCBD unit…

010405 organic chemistryBand gap[CHIM.ORGA]Chemical Sciences/Organic chemistryArylOrganic ChemistryChromophore010402 general chemistryPhotochemistry01 natural sciencesAcceptorCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPhenyl groupSpectroscopyTetrathiafulvaleneComputingMilieux_MISCELLANEOUS
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Structural studies of homoisoflavonoids: NMR spectroscopy, X-ray diffraction, and theoretical calculations

2010

Abstract In this article we present a detailed structural investigation for five homoisoflavonoids, molecules important from the pharmacological point of view. For studying the electron distribution as well as its influence on the physicochemical properties, NMR spectroscopy, X-ray diffraction, and theoretical calculations have been used. Nuclear magnetic shieldings obtained by using DFT calculations for optimized molecular geometries are correlated with the experimentally determined chemical shifts. The theoretical data are well in agreement with the experimental values. The single crystal X-ray structures of homoisoflavonoid derivatives 1, 3, and 4 have been solved. The molecular geometri…

010405 organic chemistryChemistryChemical shiftOrganic ChemistryIntermolecular forceNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystalMolecular geometryComputational chemistryX-ray crystallographyPhysical chemistryMoleculeSingle crystalSpectroscopyJournal of Molecular Structure
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Novel Stannatrane N(CH2CMe2O)2(CMe2CH2O)SnO-t-Bu and Related Oligonuclear Tin(IV) Oxoclusters. Two Isomers in One Crystal

2016

The syntheses of the alkanolamine N(CH2CMe2OH)2(CMe2CH2OH) (1), of the stannatrane N(CH2CMe2O)2(CMe2CH2O)SnO-t-Bu (2), and of the trinuclear tin oxocluster 3 consisting of the two isomers [(μ3-O)(O-t-Bu){Sn(OCH2CMe2)(OCMe2CH2)2N}3] (3a) and [(μ3-O)(μ3-O-t-Bu){Sn(OCH2CMe2)(OCMe2CH2)2N}3] (3b) as well as the isolation of a few crystals of the hexanuclear tin oxocluster [LSnOSn(OH)3LSnOH]2 [L = N(CH2CMe2O)2(CMe2CH2O)] (4) are reported. The compounds were characterized by 1H, 13C, 15N, and 119Sn (1–3) nuclear magnetic resonance and infrared spectroscopy, electrospray ionization mass spectrometry, and single-crystal X-ray diffraction analysis (1–4). A graph set analysis was performed for compoun…

010405 organic chemistryChemistryElectrospray ionizationAnalytical chemistryInfrared spectroscopychemistry.chemical_element010402 general chemistry01 natural sciencesGraph0104 chemical sciencesInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundDensity functional theoryAlkanolaminePhysical and Theoretical ChemistryTinInorganic Chemistry
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Interplay of hydrogen bonding and π–π interactions in the molecular complex of 2,6-lutidine N-oxide and water

2006

Abstract The crystal and molecular structure of 2,6-lutidine N-oxide monohydrate (1) has been determined by X-ray diffraction analysis. Each water molecule is acting as bridging ligand between the N→O moieties of two 2,6-lutidine N-oxide molecules through moderate strong intermolecular hydrogen bonding (O–H⋯O, O⋯O distances are 2.787(2) and 2.832 (2) A) giving rise to a one-dimensional (1D) polymeric helical chain. A two-dimensional (2D) layered network is then formed by self-assembly of 1D helical chains via strong π–π interactions of the aromatic rings (interplanar distances 3.385 A). The molecular structure of 1 is compared with that for the already reported molecular structures of 2-ace…

010405 organic chemistryChemistryHydrogen bondOrganic ChemistryIntermolecular forceAromaticityBridging ligand010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundPyridineMolecule26-LutidineSpectroscopyJournal of Molecular Structure
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Structural Tuning and Conformational Stability of Aromatic Oligoamide Foldamers

2017

A series of aromatic oligoamide foldamers with two or three pyridine-2,6-dicarboxamide units as their main folding motifs and varying aromatic building blocks as linkers have been synthetized to study the effects of the structural variation on the folding properties and conformational stability. Crystallographic studies showed that in the solid state the central linker unit either elongates the helices and more open S-shaped conformations, compresses the helices to more compact conformations or acts as a rigid spacer separating the pyridine-2,6-dicarboxamide units, which for their part add the predictability of the conformational properties. Multidimensional NMR studies showed that, even in…

010405 organic chemistryChemistryHydrogen bondOrganic ChemistrySolid-stateGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesstructuresCatalysis0104 chemical sciencesFolding (chemistry)Crystallographyaromatic oligoamide foldamersConformational stabilityLinkerta116Chemistry: A European Journal
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