Search results for " macrocycles"

showing 9 items of 9 documents

Polyfunctional Tetraaza-Macrocyclic Ligands: Zn(II), Cu(II) Binding and Formation of Hybrid Materials with Multiwalled Carbon Nanotubes

2017

The binding properties of HL1, HL2, and HL3 ligands toward Cu(II) and Zn(II) ions, constituted by tetraaza-macrocyclic rings decorated with pyrimidine pendants, were investigated by means of potentiometric and UV spectrophotometric measurements in aqueous solution, with the objective of using the related HL-M(II) (HL = HL1–HL3; M = Cu, Zn) complexes for the preparation of hybrid MWCNT-HL-M(II) materials based on multiwalled carbon nanotubes (MWCNTs), through an environmentally friendly noncovalent procedure. As shown by the crystal structure of [Cu(HL1)](ClO4)2, metal coordination takes place in the macrocyclic ring, whereas the pyrimidine residue remains available for attachment onto the s…

Aqueous solutionMaterials sciencePyrimidine010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryPotentiometric titrationStackingGeneral ChemistryCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesArticle0104 chemical sciencesMetallcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999visual_artPolymer chemistryvisual_art.visual_art_mediumHybrid materialcarbon nanotubes copper zinc macrocycles hybrid materials functionalized carbon nanotubesACS Omega
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Partitioning of macrocyclic compounds in a cationic and an anionic micellar solution: a small-angle neutron scattering study.

2004

Following a previous investigation on partitioning of some macrocycle compounds in sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) aqueous solutions and their effect on the micellar structure, a small-angle neutron scattering (SANS) study has been performed at fixed surfactant content (0.20 mol/L) and varying macrocycle concentrations from 0.20 up to 1.0 mol/L. Conductivity measurements have been also performed in order to evaluate the effect of the presence of macrocycles on the critical micellar concentration (cmc) of the two surfactants. SANS experimental data were fitted successfully by means of a core-plus-shell monodisperse prolate ellipsoid model. It has been…

Aqueous solutionChemistryCationic polymerizationSurfactants Macrocycles SANSSurfaces and InterfacesNeutron scatteringCondensed Matter PhysicsMicelleSmall-angle neutron scatteringCrystallographychemistry.chemical_compoundPulmonary surfactantCritical micelle concentrationElectrochemistryPhysical chemistryGeneral Materials ScienceSodium dodecyl sulfateSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Solid state halogen bonded networks vs. dynamic assemblies in solution: explaining N⋯X interactions of multivalent building blocks

2015

Tetrapyridine functionalized resorcinarene macrocycles were used as multivalent building blocks for the construction of halogen bonded networks with aryl halide linkers. In the solid state, resorcinarene macrocycles and aryl halide linker molecules assembled into interpenetrated, multidimensional halogen bonded networks with porous structure caused by the 3D block scaffold of the resorcinarenes. 19F NMR spectroscopy proved halogen bond formation also in solution, as either upfield or downfield shifts were observed depending on the bivalent or monovalent halogen bond binding mode. The binding mode in solution was explained by density functional theory computations. peerReviewed

chemistry.chemical_classificationHalogen bondta114ChemistryStereochemistryAryl halideSolid-stateGeneral ChemistryResorcinareneCondensed Matter PhysicsCrystallographyhalogen bonded networksHalogenMoleculeGeneral Materials ScienceDensity functional theoryta116Linkerresorcinarene macrocyclesaryl halide linkers
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Equipping metallo-supramolecular macrocycles with functional groups: Assemblies of pyridine-substituted urea ligands

2012

A series of di-(m-pyridyl)-urea ligands were prepared and characterized with respect to their conformations by NOESY experiments and crystallography. Methyl substitution in different positions of the pyridine rings provides control over the position of the pyridine N atoms relative to the urea carbonyl group. The ligands were used to self-assemble metallo-supramolecular M(2)L(2) and M(3)L(3) macrocycles which are generated in a finely balanced equilibrium in DMSO and DMF according to DOSY NMR experiments and ESI FTICR mass spectrometry. Again, crystallography was used to characterize the assemblies. Methyl substitution in positions next to the pyridine nitrogen prevents coordination, while …

010405 organic chemistryHydrogen bondChemistryStereochemistrySupramolecular chemistryurea ligands; metallo-supramolecular macrocycles; X-ray structure; hydrogen-bonding010402 general chemistryMass spectrometry01 natural sciencesFourier transform ion cyclotron resonance0104 chemical sciencesInorganic ChemistrySubstituted ureaCrystallographychemistry.chemical_compoundPyridineUreaTwo-dimensional nuclear magnetic resonance spectroscopyta116Dalton Transactions
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Bis-urea macrocycles with a deep cavity

2015

bis-urea macrocycleskemiamolecule recognitiondeep cavity
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Large Azobenzene Macrocycles : Formation and Detection by NMR and MS Methods

2023

Azobenzene macrocycles are widely investigated as potential drug delivery systems and as part of molecular machines due to their photo-responsive properties. Herein, we detect the formation of a series of new azobenzene macrocycles that feature up to eight switchable repeating units. High-resolution mass spectrometry and ion mobility (IM) mass spectrometry experiments and 1H and diffusion-ordered spectroscopy (DOSY) NMR are used to detect the presence of the macrocycles that contain 10 to 40 aromatic rings in the gas phase and solution, respectively. The responsiveness of the Z-to-E photo-switching of the smallest of the macrocycles, exhibiting two azobenzene units and in total 10 aromatic …

large azobenzene-containing macrocyclesresponsive moleculesmassaspektrometriaspektroskopiaatsobentseeniphotoisomerizationmolekyylitmakrosyklitESI-MS and IM detection
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Guest-Induced Folding and Self-Assembly of Conformationally Adaptive Macrocycles into Nanosheets and Nanotubes

2017

A conformationally adaptive macrocycle is presented, namely zorb[4]arene, which exists in multiple conformations in the uncomplexed state. The binding cavity of zorb[4]arene is concealed, either due to a collapsed conformation or by self-inclusion. The zorb[4]arene with long alkyl chains manifests itself with surprisingly low melting point and thus exist as an oil at room temperature. Binding of a guest molecule induces the folding and conformational rigidity of zorb[4]arene and leads to well-defined three-dimensional structures, which can further self-assemble into nanosheets or nanotubes upon solvent evaporation, depending on guest molecules and the conformations they can induce.

chemistry.chemical_classificationadaptive macrocyclesnanosheets010405 organic chemistryStereochemistryOrganic ChemistryLow melting pointGeneral Chemistry010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryguest-induced folding0104 chemical sciencesnanotubesFolding (chemistry)Solvent evaporationchemistryMoleculeSelf-assemblyta116AlkylChemistry: A European Journal
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Gold nanostars co-coated with the Cu(II) complex of a tetraazamacrocyclic ligand

2015

The twelve-membered tetraazamacrocyclic ligand L1 bears an appended lipoic acid unit, whose disulphide ring is an efficient grafting moiety for the surface of gold nanostars (GNS). The GNS that were used featured a localized surface plasmon resonance (LSPR) absorption at ∼800 nm, i.e. in the near infrared (NIR). We investigated different approaches for coating them with the Cu(2+) complex of L1. While the direct reaction of [CuL1](2+) with as-prepared GNS led to aggregation, an initial coating step with polyethyleneglycol-thiol (PEG-SH) was found to be advantageous. Displacement reactions were carried out on pegylated GNS either with [CuL1](2+), directly generating [Cun(L1@GNS)](2n+), or wi…

LuminescenceLuminescent AgentsMacrocyclic CompoundsGole nanoparticelle Cooper macrocyclesStereochemistryChemistryKineticsMetal NanoparticlesPet imagingSurface Plasmon Resonanceengineering.materialPhotothermal therapyCyclamsInorganic ChemistryCrystallographyTransmetalationCoatingCoordination ComplexesHeterocyclic CompoundsengineeringMoietyGoldSurface plasmon resonanceLuminescenceCopper
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Bis-urea macrocycles with a deep cavity.

2015

Two configurational isomers of bis-urea macrocycles have been synthesized, and their neutral molecule recognition was studied by X-ray crystallography and (1)H NMR experiments. Cooperative action between the deep cavity and the urea groups and the influence of dipole alignments on molecular recognition are discussed.

bis-urea macrocyclesChemistryStereochemistryMetals and AlloysStereoisomerismGeneral ChemistrychemistryCatalysisdeep cavitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDipolechemistry.chemical_compoundMolecular recognitionComputational chemistryMaterials ChemistryCeramics and CompositesProton NMRUreata116molecule recognitionNeutral moleculeChemical communications (Cambridge, England)
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