Search results for "Supramolecular"

showing 10 items of 830 documents

Inside Front Cover: Long-Living Light-Emitting Electrochemical Cells - Control through Supramolecular Interactions (Adv. Mater. 20/2008)

2008

Organic semiconductorFront coverMaterials scienceMechanics of Materialsbusiness.industryMechanical EngineeringSupramolecular chemistryOLEDOptoelectronicsGeneral Materials ScienceNanotechnologybusinessElectrochemical cellAdvanced Materials
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DNA Binding Studies and Cytotoxicity of a Dinuclear PtII Diazapyrenium- Based Metallo-supramolecular Rectangular Box

2012

The interaction with native DNA of a 2,7-diazapyrenium-based ligand 1 and its Pt II rectangular metal- lacycle 2 is explored through circular and linear dichroism and fluorescence spectroscopies. The metal-free ligand 1 binds through intercalation, with a binding constant of approximately 5 � 10 5 m � 1 , whereas the metallacycle 2 binds and bends the DNA with a bind- ing constant of 7 � 10 6 m � 1 . PCR assays show that metallo-supramolecular box 2 interferes with DNA transactions in vitro whereas the intercalator 1 does not. The metallacycle is active against four human cancer cell lines, with IC50 values ranging between 3.1 and 19.2 mm and shows similar levels of efficacy, but a differen…

Organoplatinum CompoundsCell SurvivalStereochemistryIntercalation (chemistry)Molecular ConformationSupramolecular chemistryAntineoplastic AgentsApoptosisLigandsNucleic Acid DenaturationLinear dichroismCatalysissupramolecular chemistryInhibitory Concentration 50chemistry.chemical_compoundCell Line TumorSettore BIO/10 - BiochimicaHumansmetallodrugPlatinumnoncovalent DNA bindingChemistryCircular DichroismOrganic ChemistryDNA NeoplasmGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMetallacycleLigand (biochemistry)Binding constantFluorescenceSettore CHIM/08 - Chimica FarmaceuticaIntercalating AgentsKineticsSpectrometry FluorescenceSettore CHIM/03 - Chimica Generale E InorganicaThermodynamicscytotoxicityPtII rectangular boxCisplatinDNAPhenanthrolines
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Spin Crossover and Paramagnetic Behaviour in Two-Dimensional Iron(II) Coordination Polymers with Stilbazole Push–Pull Ligands

2009

The suitability of the stilbazole push–pull ligands, 4′-dimethylaminostilbazole (DMAS) and 4′-diethylaminostilbazole (DEAS), for the construction of bimetallic FeII–AgI/AuI cyanide-based coordination polymers that exhibit spin crossover properties is investigated. The structural and physical characterization of four novel two-dimensional FeII polymers formulated as {Fe(DMAS)2[Ag(DMAS)(CN)2]2} (1) and {Fe(L)2[M(CN)2]2} (L = DMAS, M = Au (2); DEAS, Ag (3); DEAS, Au (4)) is reported. Polymers 1 and 4 are paramagnetic over the whole range of temperatures studied (5–300 K), whereas 2 and 3 exhibit spin crossover properties.

ParamagnetismSpin crossoverChemistrySupramolecular chemistryPhysical chemistryDensity functional theoryGeneral ChemistryCrystal structureBimetallic stripQuantum chemistryMacromoleculeAustralian Journal of Chemistry
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Chiroptical Phenomena in Reverse Micelles: The Case of (1R,2S)-Dodecyl (2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium Bromide (DMEB)

2014

(1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) aggregates dispersed in carbon tetrachloride have been investigated by Fourier transform infrared (FT-IR), vibrational circular dichroism (VCD) and 1H nuclear magnetic resonance (NMR) spectroscopy at various surfactant concentration and water-to-surfactant molar ratio. Experimental data indicate that, even at the lowest investigated concentration and in absence of added water, DMEB molecules associate in supramolecular assemblies. At higher DMEB concentration the aggregates can confine water molecules, making it plausible to think that DMEB form reverse micelles and that water molecules are quite uniformly dist…

PharmacologyHydrogen bondOrganic ChemistrySupramolecular chemistryPhotochemistryMicelleCatalysisAnalytical Chemistrychemistry.chemical_compoundchemistryBromideDrug DiscoveryVibrational circular dichroismProton NMRMoleculeOrganic chemistryChirality (chemistry)SpectroscopyChirality
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Chemically Fueled Volume Phase Transition of Polyacid Microgels

2021

Abstract Microgels are soft colloids that show responsive behavior and are easy to functionalize for applications. They are considered key components for future smart colloidal material systems. However, so far microgel systems have almost exclusively been studied in classical responsive switching settings using external triggers, while internally organized, autonomous control mechanisms as found in supramolecular chemistry and DNA nanotechnology relying on fuel‐driven out‐of‐equilibrium concepts have not been implemented into microgel systems. Here, we introduce chemically fueled transient volume phase transitions (VPTs) for poly(methacrylic acid) (PMAA) microgels, where the collapsed hydr…

Phase transition540 Chemistry and allied sciencesMaterials scienceSupramolecular chemistry010402 general chemistrydissipative self-assembly01 natural sciencesnonequilibrium processesCatalysismicrogelschemistry.chemical_compoundColloidMicrogels | Hot PaperDNA nanotechnologyfuelsAutonomous controlResearch Articlespolymerschemistry.chemical_classification010405 organic chemistryMaterial systemGeneral ChemistryPolymerGeneral Medicine0104 chemical sciencesChemical engineeringMethacrylic acidchemistry540 ChemieResearch ArticleAngewandte Chemie
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Mass spectrometry of surfactant aggregates.

2012

In contrast with the enormous amount of literature produced during many decades in the field of surfactant aggregation in liquid, liquid crystalline and solid phases, only a few investigations concerning surfactant self-assembling in the gas phase as charged aggregates have been carried out until now. This lack of interest is disappointing in view of the remarkable theoretical and practical importance of the inherent knowledge. The absence of surfactant–solvent interactions makes it easier to study the role of surfactant–surfactant forces in determining their peculiar self-assembling features as well as the ability of these assemblies to incorporate selected solubilizate molecules. Thus, t…

Phase transitionLiquid crystallineChemistryAnalytical chemistrySupramolecular chemistryGeneral MedicineMass spectrometryAtomic and Molecular Physics and OpticsMass SpectrometryPhase TransitionGas phaseSurface-Active AgentsPulmonary surfactantChemical physicsSolid phasesMoleculeGasesSpectroscopyEuropean journal of mass spectrometry (Chichester, England)
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Efficient light-induced phase transitions in halogen-bonded liquid crystals

2016

Here, we present a new family of light-responsive, fluorinated supramolecular liquid crystals (LCs) showing efficient and reversible light-induced LC-to-isotropic phase transitions. Our materials design is based on fluorinated azobenzenes, where the fluorination serves to strengthen the noncovalent interaction with bond-accepting stilbazole molecules, and increase the lifetime of the cis-form of the azobenzene units. The halogen-bonded LCs were characterized by means of X-ray diffraction, hot-stage polarized optical microscopy, and differential scanning calorimetry. Simultaneous analysis of light-induced changes in birefringence, absorption, and optical scattering allowed us to estimate tha…

Phase transitionMaterials scienceGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesArticlechemistry.chemical_compoundDifferential scanning calorimetryLiquid crystalMaterials ChemistryMoleculeHalogen Bonding Liquid Crystals Photoresponsive Supramolecular Chemistryta216ta116ta215Birefringenceta114General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyAzobenzenechemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieAbsorption (chemistry)0210 nano-technology
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Charge-Separation and Charge-Recombination Rate Constants in a Donor–Acceptor Buckybowl-Based Supramolecular Complex: Multistate and Solvent Effects

2021

The kinetics of the nonradiative photoinduced processes (charge-separation and charge-recombination) experimented in solution by a supramolecular complex formed by an electron-donating bowl-shaped truxene-tetrathiafulvalene (truxTTF) derivative and an electron-accepting fullerene fragment (hemifullerene, C30H12) has been theoretically investigated. The truxTTF·C30H12 heterodimer shows a complex decay mechanism after photoexcitation with the participation of several low-lying excited states of different nature (local and charge-transfer excitations) all close in energy. In this scenario, the absolute rate constants for all of the plausible charge-separation (CS) and charge-recombination (CR)…

PhotoexcitationReaction rate constantFullereneChemistryExcited stateSupramolecular chemistryCharge (physics)Electronic structurePhysical and Theoretical ChemistrySolvent effectsMolecular physicsArticleThe Journal of Physical Chemistry. a
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A coumarin based gold(i)-alkynyl complex: a new class of supramolecular hydrogelators.

2014

A phosphine-gold(I)-alkynyl-coumarin complex, [Au{7-(prop-2-ine-1-yloxy)-1-benzopyran-2-one}(DAPTA)] (1), was synthesized and the formation of long luminescent fibers in solution was characterized via fluorescence microscopy and dynamic light scattering. The fibers presented strong blue and green luminescence, suggesting that the gold(I) in the complex increased intersystem crossing due to the heavy atom effect, resulting in a significant increase in triplet emission. The X-ray structure of the fibers indicates that both aurophilic, π–π interactions and hydrogen bonding contribute to their formation in aqueous solvents.

PhotoluminescenceAqueous solutionChemistryHydrogen bondOrganic ChemistrySupramolecular chemistryPhotochemistryBiochemistrycoumarin basedMetalIntersystem crossingDynamic light scatteringvisual_artgold(I)-alkynyl complexvisual_art.visual_art_mediumPhysical and Theoretical ChemistryhydrogelatorsLuminescenceta116supramolecularOrganicbiomolecular chemistry
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Photoluminescence Enhancement of CdSe Quantum Dots: A Case of Organogel–Nanoparticle Symbiosis

2012

Highly fluorescent organogels (QD-organogel), prepared by combining a pseudopeptidic macrocycle and different types of CdSe quantum dots (QDs), have been characterized using a battery of optical and microscopic techniques. The results indicate that the presence of the QDs not only does not disrupt the supramolecular organization of the internal fibrillar network of the organogel to a significant extent, but it also decreases the critical concentration of gelator needed to form stable and thermoreversible organogels. Regarding the photophysical properties of the QDs, different trends were observed depending on the presence of a ZnS inorganic shell around the CdSe core. Thus, while the core-s…

PhotoluminescenceSupramolecular chemistryNanoparticleNanotechnologyINGENIERÍAS Y TECNOLOGÍASQUANTUM DOTSBiochemistryFluorescenceCatalysisZinc sulfidechemistry.chemical_compoundColloid and Surface ChemistrySemiconductor quantum dotsORGANOGELNanotecnologíaChemistryCadmium compoundsGeneral ChemistryNano-materialesFluorescenceZinc sulfideChemical engineeringQuantum dotPHOTOLUMINESCENCEHybrid materialsHybrid materialLuminescenceJournal of the American Chemical Society
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