Search results for "supramolecular"

showing 10 items of 830 documents

1H-, 13C-, and 15N-NMR and ESI-TOF+ MS studies of a supramolecular complex of silver(I) and a cholaphane

2003

A novel application of the mixed anhydride procedure for synthesising lithocholic acid piperazine diamide, an important intermediate in designing bile acid-based supramolecular host molecules, is reported. The synthesis of a thiophene-containing cholaphane with transition metal complexation ability and 1H-, 13C-, and 15N-NMR as well as ESI-TOF+ MS spectral characterisation of the ligand and its Ag(I) complex are included. The coordination of the Ag(I) ion as well as an ability of the cholaphane to recognise Ag(I) ion over alkali metal ions, especially potassium ion, is discussed. The possible medical applications are also presented.

Lithocholic acidLigandOrganic ChemistryInorganic chemistrySupramolecular chemistryBiochemistryCombinatorial chemistryIonInorganic Chemistrychemistry.chemical_compoundPiperazinechemistryTransition metalMaterials ChemistryThiopheneMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Systematic Modulation of the Supramolecular Gelation Properties of Bile Acid Alkyl Amides

2018

The self-assembly properties of nine low-molecular-weight gelators (LMWGs) based on bile acid alkyl amides were studied in detail. Based on the results, the number of hydroxyl groups attached to the steroidal backbone plays a major role in the gelation, although the nature of the aliphatic side chain also modulates the gelation abilities. Of the 50 gel systems studied, 35 are based on lithocholic acid and 15 on cholic acid derivatives. The deoxycholic acid derivatives did not form any gels. The gelation occurred primarily in aromatic solvents and the gels manifested typical fibrous or spherical morphologies. The 13C cross-polarized magic angle spinning (CPMAS) NMR spectra measured on the cr…

Lithocholic acidSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAmidebile acid amidesPolymer chemistrysupramolekulaarinen kemiaSide chainMagic angle spinningNMR-spektroskopiata116AlkylX-ray crystallographygeelitchemistry.chemical_classificationintermolecular interactionsOrganic ChemistryDeoxycholic acidsupramolecular gelsCholic acidGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryamidit0210 nano-technologyröntgenkristallografiaChemistry – A European Journal
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Supramolecular architectures formed by co-crystallization of bile acids and melamine

2010

Supramolecular multicomponent crystals constructed from three different bile acids (viz. lithocholic, deoxycholic and cholic acid) and melamine have been prepared and the non-covalent interactions in the crystals studied. Both salts and co-crystals were found. While deoxycholic and cholic acid co-crystallized with melamine as a 1 : 1 isostructural molecular complexes in space group C2, lithocholic acid formed with melamine a 2 : 1 molecular complex in space group P21. This is the first report on a multicomponent crystal structure containing lithocholic acid.

Lithocholic acidSupramolecular chemistryCholic acidGeneral ChemistryCrystal structureCondensed Matter Physicslaw.inventionchemistry.chemical_compoundchemistrylawOrganic chemistryGeneral Materials ScienceCrystallizationIsostructuralMelamineCrystEngComm
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Luminescent supramolecular heterometallic macrocycles and their encapsulation on cholate gels

2018

The metal complex formed by coordination of Zn(II) to 1,7-bis(4-methylpyridine)-4-(2- naphthylmethyl)-1,4,7-triazaheptane (ZnL2+) was reacted in aqueous solution with [Pd(NO3)2(en)] and [Pt(NO3)2(en)] salts to form the self-assembled heterometallic macrocycles [Zn2L2Pd2(en)2]8+ and [Zn2L2Pt2(en)2]8+, respectively. Pd(II) and Pt(II)- coordination modulates the original emission of ZnL2+ arising from the presence of the naphthalene chromophore and the formation of the macrocycles can be monitored due to the PET process occurring with coordination of Pd(II) and Pt(II) to the pyridine units of ZnL2+. Additionally, several studies reveal that these heteromacrocycles can be encapsulated in Zn(II)…

LuminescenceGels (Farmàcia)ChemistrySupramolecular chemistryLuminescència02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesQuímica supramolecular0104 chemical sciencesEncapsulation (networking)Inorganic ChemistryChemical engineeringSelf-assembly0210 nano-technologyLuminescenceSupramolecular chemistryGels (Pharmacy)
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Coordination networks incorporating halogen-bond donor sites and azobenzene groups

2016

Two Zn coordination networks, {[Zn(1)(Py)2]2(2-propanol)}n (3) and {[Zn(1)2(Bipy)2](DMF)2}n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized. Obtaining 3 and 4 confirms that it is possible to use a ligand wherein its coordination bond acceptor sites and XB donor sites are on the same molecular scaffold (i.e., an aromatic ring) without interfering with each other. We demonstrate that XBs play a fundamental role in the architectures and properties of the obtained coordination networks. In 3, XBs promote the formation of 2D supramolecular layers, which, by overlapping each other, allow the incorporation of 2-propanol as a gues…

MOF Supramolecular Chemistry Halogen Bonding AzobenzeneStereochemistry116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistryRing (chemistry)01 natural sciencesIUPAC RECOMMENDATIONS 2013chemistry.chemical_compoundMETAL-ORGANIC FRAMEWORKSdell'Università e della RicercaCHEMISTRYTO-CRYSTAL ISOMERIZATIONMinistero dell'IstruzioneMoleculeGeneral Materials Scienceta215SUPRAMOLECULAR SYNTHESISHalogen bondMETAL-ORGANIC FRAMEWORKS; IUPAC RECOMMENDATIONS 2013; TO-CRYSTAL ISOMERIZATION; SUPRAMOLECULAR SYNTHESIS; VISIBLE-LIGHT; POLYMERS; FLUOROAZOBENZENES; COCRYSTALS; COMPLEXES; CHEMISTRYLigandChemistryFLUOROAZOBENZENESMinistero dell'Istruzione dell'Università e della RicercaGeneral ChemistryCOCRYSTALS021001 nanoscience & nanotechnologyCondensed Matter PhysicsAcceptor0104 chemical sciencesCrystallographyAzobenzeneMIURMetal-organic frameworkCOMPLEXESSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVISIBLE-LIGHTPOLYMERS0210 nano-technology
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A modular "toolbox" approach to flexible branched multimacrocyclic hosts as precursors for multiply interlocked architectures.

2008

Tetralactam macrocycles can be functionalized by a variety of cross-coupling reactions. A modular “toolbox” strategy is presented that allows 1) several tetralactam macrocycles to be covalently connected with each other or with a central spacer, 2) the macrocycles to be substituted with or connected to different chromophores, and 3) metal-coordination sites to be attached to the macrocycles. With this approach a series of different oligo-macrocyclic hosts was obtained with great structural diversity and enormous potential for further functionalization. Rotaxanes made on the basis of these macrocycles have been synthesized to demonstrate their utility in building more complex supramolecular …

Macrocyclic CompoundsLactamsMolecular StructureRotaxanesbusiness.industryChemistryOrganic ChemistryCatenaneSupramolecular chemistryMolecular ConformationStructural diversityNanotechnologyGeneral ChemistryModular designCrystallography X-RayCombinatorial chemistryCatalysisToolboxCyclizationLuminescent MeasurementsSpectroscopy Fourier Transform InfraredbusinessChemistry (Weinheim an der Bergstrasse, Germany)
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Supramolecular assembly of functional peptide-polymer conjugates.

2019

The following review gives an overview about synthetic peptide-polymer conjugates as macromolecular building blocks and their self-assembly into a variety of supramolecular architectures, from supramolecular polymer chains, to anisotropic 1D arrays, 2D layers, and more complex 3D networks. A selection of recent literature examples using linear, coiled-coil and cyclic peptide motifs is provided. The reversible nature of the unimer-to-supramolecular polymer transition provides unique opportunities to investigate mechanistic aspects of the supramolecular assembly, with respect to the thermodynamic or kinetic parameters and furthermore provides exciting opportunities for non-equilibrium assembl…

Macromolecular SubstancesPolymersSupramolecular chemistryNanotechnologymacromolecular substances02 engineering and technology010402 general chemistry01 natural sciencesBiochemistrySupramolecular assemblyMoleculeHumansPhysical and Theoretical Chemistrychemistry.chemical_classificationMolecular StructureChemistryOrganic Chemistrytechnology industry and agriculturePolymer021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymers0210 nano-technologyPeptidesFunction (biology)MacromoleculeConjugateOrganicbiomolecular chemistry
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Synergistic assembly of hyperbranched polyethylenimine and fatty acids leading to unusual supramolecular nanocapsules

2005

Self-assembly of hyperbranched polyethylenimine (PEI) and fatty acids leads to supramolecular inverted micellar structures that are able to irreversibly transfer water-soluble guest molecules into organic solvents. Perez Prieto, Julia, Julia.Perez@uv.es ; Stiriba, Salah Eddine, Salah.Stiriba@uv.es

Macromolecular SubstancesUNESCO::QUÍMICAAssemblyAssembly ; Hiperbranched polyethylenimine ; Spramolecular ; Water-soluble ; Organic solventsSupramolecular chemistrymacromolecular substances:QUÍMICA [UNESCO]CatalysisNanocapsuleschemistry.chemical_compoundPolymer chemistryMaterials ChemistryPolyethyleneimineMoleculeSpramolecularPolyethylenimineNanotubesMolecular StructureFatty Acidstechnology industry and agricultureMetals and AlloysWaterWater-solubleGeneral ChemistryUNESCO::QUÍMICA::Química macromolecularHiperbranched polyethylenimineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrganic solventsModels ChemicalchemistrySolventsCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]lipids (amino acids peptides and proteins)Chem. Commun.
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Spectral and microscopic study of self-assembly of novel cationic spermine amides of betulinic acid

2016

Supramolecular characteristics of two spermine amides of betulinic acid (1 and 2) were studied by measuring and evaluating their UV-VIS-NIR spectra in aqueous acetonitrile and DOSY-NMR spectra in tetradeuteromethanol, accompanied by atomic force microscopy (AFM) images, scanning electron microscopy (SEM) micrographs, and transmission electron microscopy (TEM) micrographs. Fibrous supramolecular self-assembly of 1 and 2 was observed by AFM images, as well as by the SEM and TEM micrographs. Bathochromic shifts of the absorbance maximum at 870nm to 1015-970nm in the UV-VIS-NIR spectra were observed with increasing water content in the acetonitrile/water systems, indicating formation of fibrous…

Magnetic Resonance SpectroscopyScanning electron microscopeClinical BiochemistrySupramolecular chemistrymacromolecular substancesDOSY-NMRMicroscopy Atomic Force010402 general chemistry01 natural sciencesBiochemistryAbsorbancechemistry.chemical_compoundEndocrinologyMicroscopy Electron TransmissionBathochromic shiftBetulinic AcidAcetonitrileta116Molecular BiologyPharmacologyAqueous solutionMolecular Structure010405 organic chemistryChemistryOrganic Chemistryta1182technology industry and agricultureAmidesTriterpenes0104 chemical sciencesCrystallographyTransmission electron microscopySEMTEMSpermineMicroscopy Electrochemical ScanningAFMPentacyclic TriterpenesChirality (chemistry)Steroids
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SUPRAMOLECULAR ASSOCIATION OF RECOMBINANT HUMAN GROWTH HORMONE WITH HYDROPHOBIZED POLYHYDROXYETHYLASPARTAMIDES

2008

Abstract The protein delivery properties of polymer supramolecular assemblies were investigated by using recombinant human growth hormone (rh-GH) and two polyhydroxyethylaspartamide (PHEA) derivatives: (a) PHEA-C 16 obtained by PHEA random grafting with hexadecylalkylamine; (b) PHEA-PEG 5000 -C 16 obtained by PHEA random co-grafting with hexadecylalkylamine and 5 kDa poly(ethylene glycol). The two polymers possessed similar self-assembling properties: critical micelle concentration (CMC) and particle size. The protein loading (protein/polymer, w/w, %) was 12.1 ± 1.3% and 8.5 ± 0.4% with PHEA-C 16 and PHEA-PEG 5000 -C 16 , respectively. The rh-GH/polymer association constant calculated by Sc…

Malechemistry.chemical_classificationHuman Growth HormoneSupramolecular chemistryPharmaceutical ScienceGeneral MedicinePolymerProtein delivery supramolecular assembly growth hormone polyhydroxyethylaspartamideDissociation (chemistry)Polyethylene GlycolsRatsSupramolecular assemblychemistry.chemical_compoundDrug Delivery SystemschemistryPolymer ratioCritical micelle concentrationAnimalsOrganic chemistryPeptidesDrug carrierEthylene glycolCells CulturedBiotechnologyNuclear chemistry
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