Search results for "Supramolecular"

showing 10 items of 830 documents

Supramolecular Polymers: Flexible Chirality in Self-Assembled N -Annulated Perylenedicarboxamides (Small 20/2017)

2017

BiomaterialsSupramolecular polymerschemistry.chemical_classificationCircular dichroismCrystallographyMaterials scienceConvective flowchemistryGeneral Materials ScienceGeneral ChemistryChirality (chemistry)BiotechnologySelf assembledSmall
researchProduct

How Ionic Liquid Gels Work on the Removal of Bisphenol A from Wastewater

2022

The occurrence of emerging pollutants in water bodies is a pressing issue of modern society and identifying materials to remove them is the main target of current research. In this work, we prepared and characterized supramolecular gels of 1,3:2,4-dibenzylidene-d-sorbitol (DBS) in ionic liquids differing for the anion and the aliphatic or aromatic nature of the cation. We characterized our gels for their thermal stability and mechanical properties. We also found that all gels self-heal in 24 h after being cut by a razor blade. We then used our gels as sorbents to remove bisphenol A, an endocrine disruptor compound, from aqueous solutions. All gels adsorb BPA with high removal efficiencies, …

Biomaterialsionic liquidsPolymers and Plasticsadsorptionemergent pollutantsMaterials Chemistrysupramolecular gelsSettore CHIM/06 - Chimica OrganicaBPAElectronic Optical and Magnetic Materials
researchProduct

Long-Living Emitting Electrochemical Cells Based on Supramolecular π-π Interactions

2009

AbstractThe complex [Ir(ppy)2(dpbpy)][PF6] (Hppy = 2-phenylpyridine, dpbpy = 6,6'-diphenyl-2,2'-bipyridine) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs). The complex exhibits two intramolecular face-to-face π-stacking interactions and long-lived LECs have been constructed; the device characteristics are not significantly improved in comparison to analogous LECs with 6-phenyl-2,2'-bipyridine with only one π-stacking interaction.

Bipyridinechemistry.chemical_compoundMaterials sciencechemistryIntramolecular forceSupramolecular chemistryElectroluminescenceLuminescencePhotochemistryElectrochemical cellMRS Proceedings
researchProduct

Segregation of lipid in Ir-dye/DMPA mixed monolayers as strategy to fabricate 2D supramolecular nanostructures at the air–water interface

2008

A novel pseudospherical fluorinated iridium(III) derivative, Ir-dye/PF6, [Ir(F2-ppy)2(bpy)]PF6 (F2-ppy = 2-(2,4-difluoro)phenylpyridine, bpy = 2,2′-bipyridine), has been organized by using a lipid matrix, DMPA (dimyristoyl-phosphatidic acid), in several molar ratios at the air–water interface. The molecular organization of both components and the degree of miscibility in the different mixed films have been inferred by surface techniques such as π–A isotherms, ellipsometry, reflection spectroscopy, Brewster angle microscopy (BAM), and IR spectroscopy for the LB films, additionally the results have been discussed according to the additivity rule. The equimolecular Ir-dye/DMPA mixture leads to…

Brewster's angleChemistrySupramolecular chemistrychemistry.chemical_elementInfrared spectroscopyGeneral ChemistrySurface pressureMiscibilitysymbols.namesakeChemical engineeringEllipsometryMonolayerMaterials ChemistrysymbolsOrganic chemistryIridiumJournal of Materials Chemistry
researchProduct

One-Pot Synthesis and AFM Imaging of a Triangular Aramide Macrocycle

2014

Macrocyclizations in exceptionally good yields were observed during the self-condensation of N-benzylated phenyl p-aminobenzoates in the presence of LiHMDS to yield three-membered cyclic aramides that adopt a triangular shape. An ortho-alkyloxy side chain on the N-benzyl protecting group is necessary for the macrocyclization to occur. Linear polymers are formed exclusively in the absence of this Li-chelating group. A model that explains the lack of formation of other cyclic congeners and the demand for an N-(o-alkoxybenzyl) protecting group is providedon the basis of DFT calculations.High-resolution AFM imaging of the prepared molecular triangles on a calcite(10.4) surface shows individual …

Bridged-Ring CompoundsModels MolecularMacrocyclic CompoundsSurface PropertiesStereochemistryOne-pot synthesisSupramolecular chemistryMicroscopy Atomic Force010402 general chemistry53001 natural sciencesBiochemistryCatalysisCalcium CarbonateColloid and Surface ChemistrySide chainCombinatorial Chemistry TechniquesMoleculeProtecting groupbiology010405 organic chemistryHydrogen bondChemistryAryleneHydrogen BondingGeneral Chemistrybiology.organism_classificationAramides0104 chemical sciencesCrystallographyCyclizationBenzamidesDimerization
researchProduct

Supramolecular Construction of Cyanide-Bridged Re I Diimine Multichromophores

2019

The reactions of labile [Re(diimine)(CO)3(H2O)]+ precursors (diimine = 2,2′-bipyridine, bpy; 1,10-phenanthroline, phen) with dicyanoargentate anion produce the dirhenium cyanide-bridged compounds [{Re(diimine)(CO)3}2CN)]+ (1 and 2). Substitution of the axial carbonyl ligands in 2 for triphenylphosphine gives the derivative [{Re(phen)(CO)2(PPh3)}2CN]+ (3), while the employment of a neutral metalloligand [Au(PPh3)(CN)] affords heterobimetallic complex [{Re(phen)(CO)3}NCAu(PPh3)]+ (4). Furthermore, the utilization of [Au(CN)2]−, [Pt(CN)4]2–, and [Fe(CN)6]4–/3– cyanometallates leads to the higher nuclearity aggregates [{Re(diimine)(CO)3NC}xM]m+ (M = Au, x = 2, 5 and 6; Pt, x = 4, 7 and 8; Fe, x…

CARBONYL-COMPLEXESSPECTROSCOPIC PROPERTIESCyanideSupramolecular chemistryEXCITED-STATECrystal structure010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundCRYSTAL-STRUCTUREPhysical and Theoretical ChemistryTriphenylphosphineta116MULTIPLE EMISSIONSDiimineDENSITY-FUNCTIONAL METHODS010405 organic chemistryLUMINESCENT RE(I)0104 chemical sciencesRHENIUM(I) TRICARBONYL COMPLEXESCrystallographychemistryExcited statePHOTOPHYSICAL PROPERTIESPhosphorescenceCOORDINATION POLYMERSDerivative (chemistry)INORGANIC CHEMISTRY
researchProduct

Red and blue luminescent metallo-supramolecular coordination polymers assembled through π–π interactions †

2000

The use of π-stacking interactions to control the aggregation of photo-active metal centres is explored through the design of bis(2,2′;6′,2′′-terpyridyl) metal complexes functionalised with biphenyl ‘tails’. Aryl–aryl interactions control the aggregation of the metal complexes into polymetallic arrays in the solid state. Cobalt(II), ruthenium(II), nickel(II), copper(II), zinc(II) and cadmium(II) bis-ligand complexes and a mixed ligand ruthenium(II) complex have been structurally characterised. The solid-state structures are dependent on which units dominate the π-stacking. For cobalt, ruthenium, nickel and copper, biphenylene–biphenylene interactions lead to linear rod-like arrays, while fo…

CadmiumSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryZincBiphenylenePhotochemistryCopperRutheniumNickelchemistry.chemical_compoundchemistryPolymer chemistryCobaltJournal of the Chemical Society, Dalton Transactions
researchProduct

Carbon Nanostructures: Covalent and Macromolecular Chemistry

2012

The aim of this introductory chapter is to bring to the attention of the readers the achievements made in the chemistry of carbon nanostructures and, mostly, in the chemistry of fullerenes, carbon nanotubes (CNTs), and the most recent graphenes. Since the discovery of fullerenes in 1985 and their further preparation in multigram amounts, the chemistry and reactivity of thesemolecular carbon allotropes have been well established. Actually, this chemical reactivity has been used as a benchmark for further studies carried out in the coming carbon nanotubes (single andmultiple wall) and graphenes. Assuming that the fundamental chemistry of fullerenes is known and basically corresponds to that o…

Carbon nanostructuresMaterials scienceFullereneSupramolecular chemistrychemistry.chemical_elementCarbon nanotubelaw.inventionchemistrylawCovalent bondPolymer chemistrySurface modificationReactivity (chemistry)CarbonSupramolecular Chemistry of Fullerenes and Carbon Nanotubes
researchProduct

Resorcinarene Bis-Thiacrowns: Prospective Host Molecules for Silver Encapsulation

2012

Mixed-donor atom tetramethoxy resorcinarene bis-thiacrown hosts, in which the crown unit contains both hard oxygen and soft sulfur donor atoms, were synthesized for soft metal cation binding. The binding properties were investigated both in solution and in the solid state by NMR spectroscopy and X-ray crystallography. It was found that the resorcinarene bis-thiacrowns were able to complex silver cations with remarkable affinity forming readily 1:2 host–guest complexes in solution. The solid state structures also revealed that the bis-thiacrowns form silver complexes in an unanticipated endo- and exo-cavity fashion within the same host molecule. Both the solution and solid state studies indi…

Cation bindingChemistryStereochemistryOrganic ChemistryBinding propertiesSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyResorcinareneBiochemistrySulfurAtomPolymer chemistryMoleculeta116Chemistry - An Asian Journal
researchProduct

Resorcinarene bis-crown silver complexes and their application as antibacterial Langmuir-Blodgett films

2012

Silver complexes of a cation binding supramolecular host, resorcinarene bis-crown (CNBC5) with propyl, nonyl, decyl and undecyl alkyl chains were investigated by NMR titration, picrate extraction and single crystal X-ray diffraction. Binding studies showed that both 1 : 1 and 1 : 2 (host-Ag(+)) complexes are present in solution with only a slight effect of the lower rim alkyl chain length on the binding constants (log K 4.0-4.2 for 1 : 2 complexes). Solid state complexes of the resorcinarene bis-crowns bearing either C(3) or C(11) chains were obtained. Single crystal X-ray analyses showed that both derivatives bind silver ions by metal-arene and Ag···O coordination from the crown ether brid…

Cation bindingSilverPhenylalaninePicrateInorganic chemistrySupramolecular chemistryCrystallography X-RayBiochemistryLangmuir–Blodgett filmchemistry.chemical_compoundCoordination ComplexesPolymer chemistryAmphiphileEscherichia coliPhysical and Theoretical Chemistryta116Escherichia coli InfectionsAlkylCrown etherchemistry.chemical_classificationMolecular StructureOrganic ChemistryResorcinareneAnti-Bacterial AgentschemistryCalixarenesOrganic & Biomolecular Chemistry
researchProduct