Search results for "assembly"

showing 10 items of 768 documents

Effects of side chains of oxatub[4]arene on its conformational interconversion, molecular recognition and macroscopic self-assembly.

2017

A series of oxatub[4]arenes with different alkyl side chains have been synthesized. The conformational interconversion, molecular recognition and macroscopic self-assembly behaviour of oxatub[4]arene derivatives were investigated. The difference in side chains slightly changes the binding affinities, but results in different self-assembly morphologies at the solid state.

StereochemistrySolid-state010402 general chemistry01 natural sciencesCatalysisside chainsoxatubarenesMolecular recognitionMaterials ChemistrySide chainta116makromolekyylitAlkylBinding affinitieschemistry.chemical_classification010405 organic chemistryChemistryMetals and Alloysself-assemblyGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCeramics and CompositesSelf-assemblyaromaattiset hiilivedytChemical communications (Cambridge, England)
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An Octanuclear Metallosupramolecular Cage Designed To Exhibit Spin-Crossover Behavior.

2018

By employing the subcomponent self-assembly approach utilizing 5,10,15,20-tetrakis(4-aminophenyl)porphyrin or its zinc(II) complex, 1H-4-imidazolecarbaldehyde, and either zinc(II) or iron(II) salts, we were able to prepare O-symmetric cages having a confined volume of ca. 1300 Å3 . The use of iron(II) salts yielded coordination cages in the high-spin state at room temperature, manifesting spin-crossover in solution at low temperatures, whereas corresponding zinc(II) salts led to the corresponding diamagnetic analogues. The new cages were characterized by synchrotron X-ray crystallography, high-resolution mass spectrometry, and NMR, Mössbauer, IR, and UV/Vis spectroscopy. The cage structures…

Stereochemistrychemistry.chemical_elementZinc010402 general chemistryMass spectrometry01 natural sciencesCatalysislaw.inventionhost-guest systemschemistry.chemical_compoundspin crossoverlawSpin crossoverMössbauer spectroscopySpectroscopyta116010405 organic chemistryChemistryiron(II) complexesGeneral Chemistryself-assemblymetallosupramolecular chemistryPorphyrinSynchrotron0104 chemical sciencesCrystallographyDiamagnetism
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Self-assembly of 1D- and 3D-networks through non-coordination intermolecular forces: synthesis and crystal structures of copper(I) complexes based on…

2007

Reaction of [Cu2(H3CCN)2(μ-pydz)3][PF6]2 (1) with an excess of pyridazine or phthalazine yielded the novel dinuclear complexes [Cu2(μ-pydz)3(pydz)2][PF6]2 (2) and [Cu2 (μ- pydz)(μ-phtz)2(phtz)2][PF6]2 (5), respectively. Depolymerisation of the coordination polymer 1 ∞ {[Cu(μ-pydz)2][PF6]} (3) in dichloromethane by addition of an excess of benzo[c]cinnoline afforded the dinuclear copper(I) salt [Cu2(μ-pydz)2(pydz)2(benzo[c]cinnoline)2][PF6]2 (4). Furthermore, a new route for the preparation of bis(benzonitrile)tris(μ-phthalazine)dicopper(I) bis(trifluoromethanesulfonate), [Cu2(C6H5CN)2(μ-phtz)3][CF3SO3]2 (7), was established from {[Cu(CF3SO3)]2 ・C6H5Me}, phthalazine and benzonitrile via the …

Stereochemistrychemistry.chemical_elementphthalazineCrystal structure010402 general chemistry01 natural sciencesPyridazinechemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistryCinnolineComputingMilieux_MISCELLANEOUS010405 organic chemistryIntermolecular force[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral Chemistrybenzo[c]cinnolineself-assemblyCopper0104 chemical sciencescopper(I)CrystallographyBenzonitrilepyridazinechemistryPhthalazineTrifluoromethanesulfonate
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Self-assembly of metallosupramolecular rhombi from chiral concave 9,9'-spirobifluorene-derived bis(pyridine) ligands.

2014

Two new 9,9’-spirobifluorene-based bis(4-pyridines) were synthesised in enantiopure and one also in racemic form. These ligands act as concave templates and form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. The self-assembly process of the racemic ligand preferably occurs in a narcissistic self-recognising manner. Hence, a mixture of all three possible stereoisomers [(dppp)2M2{(R)-L}2](OTf)4, [(dppp)2M2{(S)-L}2](OTf)4, and [(dppp)2M2{(R)-L}{(S)-L}](OTf)4 was obtained in an approximate 1.5:1.5:1 ratio which corresponds to an amplification of the homochiral assemblies by a factor of approximately three as evidenced by NMR spectroscopy and m…

Stereochemistryconcave templatesSupramolecular chemistrymetal complexesFull Research Paperself-sortingsupramolecular chemistrylcsh:QD241-441lcsh:Organic chemistrysupramolekulaarinen kemialcsh:Scienceta1169LigandChemistryOrganic ChemistryNuclear magnetic resonance spectroscopyself-assemblyPyridine ligandCrystallographyChemistrySelf sortingEnantiopure drug99’-spirobifluorenelcsh:QSelf-assembly9’-spirobifluoreneSingle crystalBeilstein journal of organic chemistry
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Self-Sorting Effects in the Self-Assembly of Metallosupramolecular Rhombi from Chiral BINOL-Derived Bis(pyridine) Ligands

2013

Four BINOL-based bis(4-pyridyl) ligands were synthesised in enantiopure and racemic form. These ligands form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. In principle, racemic ligands can self-assemble into three stereoisomeric rhombi. The degree of self-sorting in the self-assembly process crucially depends on the substitution pattern and the resulting bend angle of the V-shaped ligands as well as the degree of steric crowding within the assembly when racemic ligands are used. Thus, these processes either lead to homochiral assemblies in a narcissistic self-recognition manner, to heterochiral assemblies in a social self-discriminating ma…

Steric effectsAtropisomerEnantiopure drugChemistryStereochemistryOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementSelf-assemblyNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryPlatinumPalladiumEuropean Journal of Organic Chemistry
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Unexpected self-assembly of a homochiral metallosupramolecular M4L4 catenane

2014

Two enantiomerically pure 9,9'-spirobifluorene-based bis(pyridine) ligands 1 and 2 were prepared to study their self-assembly behavior upon coordination to cis-protected palladium(II) ions. Whereas the sterically more demanding ligand, 2, gave rise to the expected dinuclear metallosupramolecular M2L2 rhombi, the sterically less demanding ligand, 1, acts as a template to give rise to a homochiral metallosupramolecular M4L4 catenane.

Steric effectsLigandStereochemistryOrganic ChemistryCatenanechemistry.chemical_elementGeneral ChemistryCatalysischemistry.chemical_compoundchemistryPyridinePolymer chemistrySelf-assemblyta116PalladiumChemistry: A European Journal
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Spontaneous Self-Assembly of a 1,8-Naphthyridine into Diverse Crystalline 1D Nanostructures: Implications on the Stimuli-Responsive Luminescent Behav…

2014

The previously reported organic solid-state fluorophore 7-(3,4-dimethoxyphenyl)-2-ethoxy-4-phenyl-1,8-naphthyridine-3-carbonitrile 1 was found to spontaneously self-organize into diverse 1D crystalline nanostructures by choosing appropriate liquid phase self-assembly conditions. Experimental results, as well as DFT quantum calculations (at the M06-2X/6-31+G(d) level), shed light on the aggregation mechanism. This was found in good agreement with molecules being primarily joined together through intermolecular alignment caused by electrostatic interactions, as well as minimization of the steric repulsions. This alignment provokes the preferential growth of the crystalline materials into 1D a…

Steric effectsMaterials scienceFluorophoreIntermolecular forceNanowireGeneral ChemistryCondensed Matter PhysicsFluorescenceCrystallographychemistry.chemical_compoundchemistryChemical physicsMoleculeGeneral Materials ScienceSelf-assemblyLuminescenceCrystal Growth & Design
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Noncovalent assembly of functional groups on calix[4]arene molecular boxes

1997

Calix[4]arenes diametrically substituted at the upper rim with two melamine units spontaneously form well-defined box-like assemblies in the presence of two equivalents of 5,5-diethylbarbituric acid. These assemblies, consisting of nine different components, are held together by 36 hydrogen bonds and are stable in apolar solvents at concentrations of up to 10-4M. This paper reports the first X-ray crystal structure, and the MALDI TOF mass spectra together with the complete 1H NMR spectroscopic characterization of these hydrogen-bonded assemblies. The crystal structure clearly shows that the assemblies are stereogenic, as a result of the antiparallel orientation of the two rosette motifs. Fu…

Steric effectsNoncovalent assemblyMolecular boxesChemistryHydrogen bondStereochemistryOrganic ChemistrySupramolecular chemistryGeneral ChemistryAntiparallel (biochemistry)CatalysisSupramolecular ChemistryStereocenterHydrogen bondsCrystallographyIntramolecular forceCalixareneProton NMRCalixarenesChemistry : a European journal
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Self-assembly in surfactant-based mixtures driven by acid–base reactions: bis(2-ethylhexyl) phosphoric acid–n-octylamine systems

2013

Structural and dynamic features of bis(2-ethylhexyl) phosphoric acid (HDEHP)-n-octylamine (NOA) mixtures as a function of the NOA mole fraction (X-NOA) have been investigated by SAXS, WAXS, IR, dielectric spectroscopy and polarized optical microscopy. In the 0 <= X-NOA < 0.5 range, mixtures are transparent liquids, while the abrupt formation of a waxy solid characterized by an hexagonal bidimensional structure occurs at X-NOA = 0.5. Such a composition-induced phase transition results from the synergetic effect of the progressive increase in number density of ordered HDEHP-NOA nanodomains with X-NOA. Mainly driven by an HDEHP to NOA proton transfer, the increase of structural order with X-NO…

Steric effectsPhase transitionself-assembly surfactant mixtures nanostructures dynamical propertiesReversed micelles liquid crystals phosphate dielectric spectroscopyChemistrySmall-angle X-ray scatteringGeneral Chemical EngineeringReversed micellesGeneral ChemistryMole fractionDielectric spectroscopychemistry.chemical_compoundCrystallographyliquid crystalsChemical engineeringPulmonary surfactantSelf-assemblydielectric spectroscopyPhosphoric acidSettore CHIM/02 - Chimica FisicaphosphateRSC Advances
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Molecular Mechanisms Controlling the Self-Assembly Process of Polyelectrolyte Multilayers

1998

The distance dependent interaction between polyelectrolyte-covered mica surfaces in aqueous solution was investigated with the surface forces apparatus. We find the following:  (i) The surface charge changes sign, when an oppositely charged polyelectrolyte from a concentrated polyelectrolyte solution is adsorbed. (ii) Tails and loops of the adsorbed polyions dangle into the bulk phase, inducing a small steric force. If polycations and poyanions are adsorbed on top of each other, a strong short range attractive force is seen due to ion-pair formation after crossing a large repulsive electrostatic/steric barrier. (iii) Obviously, after polyelectrolyte adsorption, there are still nonoccupied b…

Steric effectsPolymers and PlasticsChemistryOrganic ChemistrySurface forces apparatusPolyelectrolyteInorganic ChemistryAdsorptionPolyelectrolyte adsorptionChemical physicsPhase (matter)Polymer chemistryMaterials ChemistrySelf-assemblySurface chargeMacromolecules
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