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showing 10 items of 55700 documents

The substituent effect of π-electron delocalization in N-methylamino-nitropyridine derivatives: crystal structure and DFT calculations

2020

AbstractThe crystal and molecular structures of 3-(N-methylamino)-2-nitropyridine, 5-(N-methylamino)-2-nitropyridine and 2-(N-methylamino)-5-nitropyridine have been characterized by X-ray diffraction. To perform conformational analysis, the geometries of the compounds as well as their conformers and rotamers were optimized at the B3LYP/6-311++G(3df,3pd) level. The resulting data were used to analyze the π-electron delocalization effect in relation to the methylamino group rotation in ortho-, meta- and para-substitution positions. Quantitative aromaticity indices were calculated based on which we estimated the electronic structures of the analyzed compounds. The substituent effect of the met…

010405 organic chemistryAromaticityCrystal structureSubstituentAromaticityCrystal structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)DFT calculations01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundDelocalized electronSubstituent effectchemistryCharge of the substituent active regionIntramolecular forcePyridineSubstituent effect stabilization energyPhysical and Theoretical ChemistryConformational isomerismStructural Chemistry
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Cooperative N–H bond activation by amido-Ge(ii) cations

2020

N-heterocyclic carbene (NHC) and tertiary phosphine-stabilized germylium-ylidene cations, [R(L)Ge:]+, featuring tethered amido substituents at R have been synthesized via halide abstraction. Characterization in the solid state by X-ray crystallography shows these systems to be monomeric, featuring a two-coordinate C,N- or P,N-ligated germanium atom. The presence of the strongly Lewis acidic cationic germanium centre and proximal amide function allows for facile cleavage of N-H bonds in 1,2-fashion: the products resulting from reactions with carbazole feature a tethered secondary amine donor bound to a three-coordinate carbazolyl-GeII centre. In each case, addition of the components of the N…

010405 organic chemistryCarbazoleHydrogen bondCationic polymerizationchemistry.chemical_elementGermaniumSubstrate (electronics)010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAmideAmine gas treatingCarbeneDalton Transactions
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Dual role of silver in a fluorogenic N-squaraine probe based on Ag(i)–π interactions

2021

In the presence of Ag(I), the monoanion of cyano-N-squaraine (I) generates an intense fluorescence turn-on response. Experimental evidence and DFT calculations reveal a sequence of deprotonation-coordination events in which the Ag(I) ions play a dual role as a Lewis acid and coordinating metal. The observed effect is highly selective for Ag(I) compared to other metals.

010405 organic chemistryChemistry010402 general chemistryHighly selective01 natural sciences0104 chemical sciencesIonInorganic ChemistryMetalCrystallographyDual rolevisual_artIntense fluorescencevisual_art.visual_art_mediumLewis acids and basesSequence (medicine)Dalton Transactions
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An aryl-fused redox-active tetrathiafulvalene with enhanced mixed-valence and radical-cation dimer stabilities.

2018

Molecular recognition of stable organic radicals is a relatively novel, but important structural binding motif in supramolecular chemistry. Here, we report on a redox-switchable veratrole-fused tetrathiafulvalene derivative VTTF which is ideally suited for this purpose and for the incorporation into stimuli-responsive systems. As revealed by electrochemistry, UV/Vis measurements, X-ray analysis, and electrocrystallisation, VTTF can be reversibly oxidised to the corresponding radical-cation or dication which shows optoelectronic and structural propterties similar to tetrathiafulvalene and tetrakis(methylthio)tetrathiafulvalene. However, theoretical calculations, variable temperature EPR, and…

010405 organic chemistryChemistryArylDimerRadicalOrganic ChemistrySupramolecular chemistry010402 general chemistry01 natural sciencesBiochemistrysupramolecular chemistry0104 chemical scienceslaw.inventionDicationchemistry.chemical_compoundCrystallographyRadical ionlawsupramolekulaarinen kemiaPhysical and Theoretical ChemistryElectron paramagnetic resonanceta116TetrathiafulvaleneOrganicbiomolecular chemistry
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Syntheses, Properties and Structures of [{(C 5 Me 5 ) 2 Nb} 2 NiTe 4 ] and [( t BuC 5 H 4 Nb) 2 Ni 5 Te 7 (Ph 2 PCH 2 PPh 2 ) 2 ]: The Quest for Tetr…

2007

The reaction of [Ni(COD) 2 ] with [Cp* 2 NbTe 2 H] (1; Cp * = η-C 5 Me 5 ) in the presence of Ph 2 PCH 2 PPh 2 (dppm) in boiling toluene gives black-violet [(Cp * 2 Nb) 2 NiTe 4 ] (3). If [Cp' 2 NbTe 2 H] (2; Cp' = tBuC 5 H 4 ) is used under similar conditions dark-brown [(Cp'Nb)2Ni5Te7(dppm)2] (4) is formed. The structures of 3 and 4 have been determined crystallographically. Complex 3 contains a severely distorted NiTe 4 tetrahedron to which two niobocene groups are coordinated. Density functional analysis of the electronic structure of the NiTe 4 building block shows that it is best described as an [Ni(η 2 -Te 2 ) 2 ] 2- fragment. The structure of 4 reveals the presence of two Ni 5 and T…

010405 organic chemistryChemistryCationic polymerizationchemistry.chemical_elementElectronic structure010402 general chemistryElectrochemistry01 natural sciencesRedox0104 chemical sciencesInorganic ChemistryParamagnetismCrystallographyNickelTetragonal crystal systemTelluriumEuropean Journal of Inorganic Chemistry
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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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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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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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Practical Syntheses of Terrylene Chromophores from Naphthalene and Perylene Building Blocks

2017

A facile and efficient method to synthesize terrylene imides, a unique class of chromophores, and their derivatives from commercially available naphthalene and perylene building blocks is reported. We developed an extremely efficient Suzuki/C-H-arylation coupling cascade with Pd2(dba)3/PCy3 (dba = dibenzylidenacetone, Cy = cyclohexyl) as the catalyst and highly soluble naphthalene derivatives as starting materials. This efficiency allows purification via precipitation and crystallization, avoiding time-consuming column chromatography. For the first time, the highly soluble 3,4,11,12-terrylene tetraester was prepared in gram scale with yields up to 75 % which thus becomes a versatile startin…

010405 organic chemistryChemistryGeneral ChemistryChromophore010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionCatalysischemistry.chemical_compoundColumn chromatographylawOrganic chemistryCrystallizationPeryleneNaphthaleneAdvanced Synthesis & Catalysis
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