Search results for "Molecular chemistry"

showing 10 items of 1103 documents

Solution Conformation and Self‐Assembly of Ferrocenyl(thio)ureas

2016

Conformations and (dis)assembly processes of ureas and thioureas are of fundamental importance in supramolecular chemistry, anion binding, or crystal engineering, both in solution and in the solid state. For sensing and switching processes a redox-active unit, such as the ferrocene/ferrocenium couple, is especially suitable. Here, self-assembly processes of redox-active ferrocenyl(thio)ureas FcNHC(X)NHR [X = O, R = Fc (1), Ph (2), 1-naphthyl (3), Me (4), Et (5); X = S, R = Fc (6), 1-anthracenyl (7)] through hydrogen bonds – both in the solid state and in THF and CH2Cl2 solution – are reported. Special emphasis is placed on the impact of nonclassical intramolecular NH···Fe hydrogen bonds in …

010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryThio-010402 general chemistryCrystal engineering01 natural sciencesRedox0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyFerrocenechemistryIntramolecular forceAnion bindingEuropean Journal of Inorganic Chemistry
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Ion-Pair Complexation with Dibenzo[21]Crown-7 and Dibenzo[24]Crown-8 bis-Urea Receptors

2016

Synthesis and ion-pair complexation properties of novel ditopic bis-urea receptors based on dibenzo[21]crown-7 (R(1) ) and dibenzo[24]crown-8 (R(2) ) scaffolds have been studied in the solid state, solution, and gas phase. In a 4:1 CDCl3 /[D6 ]DMSO solution, both receptors clearly show positive heterotropic cooperativity toward halide anions when complexed with Rb(+) or Cs(+) , with the halide affinity increasing in order I(-) <Br(-) <Cl(-) . In solution, the rubidium complexes of both receptors have higher halide affinities compared to the caesium complexes. However, Rb(+) and Cs(+) complexes of R(2) show stronger affinities toward all the studied anions compared to the corresponding catio…

010405 organic chemistryHydrogen bondion-pair receptorscrown ethersOrganic ChemistryInorganic chemistrySupramolecular chemistrychemistry.chemical_elementHalideCooperativityGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesditopic receptorsCatalysis0104 chemical sciencesRubidiumCrystallographychemistryCaesiumbis-urea receptorsSelectivityta116Chemistry - A European Journal
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Herbicidal value of essential oils from oregano-like flavour species

2017

ABSTRACTChemical composition and phytotoxicity of oregano, marjoram and Thymus mastichina essential oils against Portulaca oleracea L., Lolium multiflorum Lam. and Echinochloa crus-galli (L.) Beauv. has been investigated. Seventy-seven compounds reaching 97.3% and 99.4% were identified by gas chromatography–mass spectrometry. Carvacrol (60.42 ± 0.07%), p-cymene (15.52 ± 0.02%) and γ-terpinene (5.19 ± 0.02%) were the main compounds in oregano essential oil, whereas large amounts of 1,8-cineol (59.59 ± 0.85%, 49.49 ± 0.37%), linalool (13.05 ± 0.04%, 5.66 ± 0.01%) and α-terpineol (3.36 ± 0.10%, 5.59 ± 0.01%), followed by β-pinene (4.35 ± 0.39, 5.54 ± 0.01%) and α-pinene (4.11 ± 0.53, 4.28 ± 0.…

010405 organic chemistryImmunologyThymus mastichinaLolium multiflorumBiologyPortulacabiology.organism_classification01 natural sciences0104 chemical scienceslaw.invention010404 medicinal & biomolecular chemistrychemistry.chemical_compoundLinaloolchemistrylawGerminationBotanyCarvacrolPhytotoxicityFood scienceAgronomy and Crop ScienceEssential oilFood ScienceFood and Agricultural Immunology
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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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Solvent effects on the dimensionality of oxamato-bridged manganese(II) compounds

2018

Two new oxamate-containing manganese(II) complexes, [{Mn(H2edpba)(H2O)2}2]n (1) and [Mn(H2edpba)(dmso)2]∙dmso∙CH3COCH3∙H2O (2) (H4edpba = N,N′-ethylenediphenylenebis(oxamic acid) and dmso = dimethylsulfoxide), have been synthesized and the structures of 1 and 2 were characterized by single crystal X-ray diffraction. The structure of 1 consists of neutral honeycomb networks in which each manganese(II) is six-coordinate by one H2edpba2− ligand and two carboxylate–oxygens from two other H2edpba2− ligands building the equatorial plane. Each manganese is connected to its nearest neighbor through two carboxylate(monoprotonated oxamate) bridges in an anti-syn conformation. A dmso solution of singl…

010405 organic chemistryLigandSupramolecular chemistrychemistry.chemical_elementManganese010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryX-ray crystallographyMaterials ChemistryMoleculeCarboxylatePhysical and Theoretical ChemistrySolvent effectsSingle crystal
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Self‐Assembly and Characterisation of Grid‐Type Iron( II ), Cobalt( II ) and Zinc( II ) Complexes

2003

The reaction of the ligands 5 and 6, containing two tridentate binding units, with iron(II), cobalt(II) and zinc(II) leads to the self-assembly of supramolecular architectures of [2 × 2] grid type containing four ions in octahedral coordination sites. The grid-type structures have been assigned on the basis of the spectroscopic data in solution, and confirmed in the solid state in the case of complexes 6b and 6c by X-ray crystallography. The latter study revealed that each metal ion is situated in a distorted octahedral coordination environment comprising two N,N,O ligand donor sets. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

010405 organic chemistryLigandSupramolecular chemistrychemistry.chemical_elementZinc010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryMetalCrystallographychemistryOctahedronvisual_artvisual_art.visual_art_mediumSelf-assemblyCobaltEuropean Journal of Inorganic Chemistry
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Solid-State Molecular Nanomagnet Inclusion into a Magnetic Metal-Organic Framework: Interplay of the Magnetic Properties.

2015

Single-ion magnets (SIMs) are the smallest possible magnetic devices and are a controllable, bottom-up approach to nanoscale magnetism with potential applications in quantum computing and high-density information storage. In this work, we take advantage of the promising, but yet insufficiently explored, solid-state chemistry of metal-organic frameworks (MOFs) to report the single-crystal to single-crystal inclusion of such molecular nanomagnets within the pores of a magnetic MOF. The resulting host-guest supramolecular aggregate is used as a playground in the first in-depth study on the interplay between the internal magnetic field created by the long-range magnetic ordering of the structur…

010405 organic chemistryMagnetismChemistryOrganic ChemistrySupramolecular chemistryPhysics::OpticsNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesNanomagnetCatalysis0104 chemical sciencesMagnetic fieldMagnetMetal-organic frameworkNanoscopic scaleQuantum computerChemistry (Weinheim an der Bergstrasse, Germany)
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Size‐Selective Encapsulation of Hydrophobic Guests by Self‐Assembled M 4 L 6 Cobalt and Nickel Cages

2012

Subtle differences in metal-ligand bond lengths between a series of [M(4)L(6)](4-) tetrahedral cages, where M = Fe(II), Co(II), or Ni(II), were observed to result in substantial differences in affinity for hydrophobic guests in water. Changing the metal ion from iron(II) to cobalt(II) or nickel(II) increases the size of the interior cavity of the cage and allows encapsulation of larger guest molecules. NMR spectroscopy was used to study the recognition properties of the iron(II) and cobalt(II) cages towards small hydrophobic guests in water, and single-crystal X-ray diffraction was used to study the solid-state complexes of the iron(II) and nickel(II) cages.

010405 organic chemistryOrganic ChemistryInorganic chemistrySupramolecular chemistrychemistry.chemical_elementmacromolecular substancesGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesMetalBond lengthCrystallographyNickelchemistryTransition metalvisual_artvisual_art.visual_art_mediumMoleculeta116CobaltChemistry – A European Journal
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Supramolecular assemblies and photophysical properties of ionic homo- and heteronuclear metallophilic complexes

2019

Abstract The synthesis of two dinuclear ionic complexes with chemical formula [Au(PR 3 ) 2 ][Au(C ≡ CC 5 H 4 N-4) 2 ] that contain the water soluble phosphines, PR 3 , PTA (1, 3,5-triaza-7-phosphaadamantane, 1 ) and DAPTA (3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane, 2 ) is herein described. The differences on their intermolecular reorganization have been analyzed and compared with the previously reported for the neutral complexes [Au(PR 3 )(C ≡ CC 5 H 4 N-4)]. It has been evidenced that the reorganization of the ligands giving rise to the dinuclear ionic complexes produces a complete change in the properties giving rise to Au⋯Au intermolecular assemblies. These aurophilic conta…

010405 organic chemistryOrganic ChemistryIntermolecular forceSupramolecular chemistryIonic bondingOr010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryHeteronuclear moleculeHexafluorophosphateCompostos d'orMaterials ChemistryGoldPhysical and Theoretical ChemistryNonaneLuminescenceTrifluoromethanesulfonateGold compounds
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A new polyketide from the bark of Hypericum roeperianum Schimp. (Hypericaceae)

2019

The isolation and spectroscopic data of a hitherto undescribed polyketide (1) from Hypericum roeperianum Schimp. (Hypericaceae) together with six known compounds (2–7) is herein reported. The struc...

010405 organic chemistryOrganic ChemistryPlant ScienceBiologyHypericaceaebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryPolyketideHypericum roeperianumvisual_artBotanyvisual_art.visual_art_mediumBarkNatural Product Research
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