Search results for "Supramolecular"

showing 10 items of 830 documents

Positive Allosteric Control of Guests Encapsulation by Metal Binding to Covalent Porphyrin Cages

2018

The allosteric control of the receptor properties of two flexible covalent cages is reported. These receptors consist of two zinc(II) porphyrins connected by four linkers of two different sizes, each incorporating two 1,2,3‐triazolyl ligands. Silver(I) ions act as effectors, responsible for an on/off encapsulation mechanism of neutral guest molecules. Binding silver(I) ions to the triazoles opens the cages and triggers the coordination of pyrazine or the encapsulation of N,N′‐dibutyl‐1,4,5,8‐naphthalene diimide. The X‐ray structure of the silver(I)‐complexed receptor with short connectors is reported, revealing the hollow structure with a cavity well‐defined by two eclipsed porphyrins. Rath…

PyrazineAllosteric regulationSupramolecular chemistryCrystal structure010402 general chemistryporphyrins01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundDiimidesupramolekulaarinen kemiaMoleculeta116010405 organic chemistryallosteric controlOrganic Chemistryhost–guest systemsGeneral ChemistryPorphyrin3. Good health0104 chemical sciencesCrystallographychemistryCovalent bondcage compounds[CHIM.OTHE]Chemical Sciences/Other
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Synthesis of Pillar[6]arenes and Their Host–Guest Complexes

2015

Pillar[n]arenes are a fast-growing research topic in supramolecular chemistry. Originally the focus was predominantly on pillar[5]arenes; however, now more and more studies on pillar[6]arenes are being performed. The ability and selectivity of host–guest complexations depend strongly on the size of the inner cavities of these macrocycles. New results have stimulated us to compile the synthetic entries and the complexations of pillar[6]arenes with large cylindric cavities that offer space for many different guest molecules. 1 Introduction 2 Preparation of Pillar[6]arenes 2.1 Pillar[6]arenes by Macrocyclization Reactions 2.2 Hydroxypillar[6]arenes through Ether Cleavage 2.3 Hydroxypillar[6]ar…

Pyridinium CompoundsChemistryOrganic ChemistrySupramolecular chemistryAlkylationCatalysisMetalvisual_artPolymer chemistryAlkoxy groupvisual_art.visual_art_mediumMoleculesense organsSelectivityEther cleavageSynthesis
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ChemInform Abstract: Synthesis of Pillar[6]arenes and Their Host-Guest Complexes

2015

Pillar[n]arenes are a fast-growing research topic in supramolecular chemistry. Originally the focus was predominantly on pillar[5]arenes; however, now more and more studies on pillar[6]arenes are being performed. The ability and selectivity of host–guest complexations depend strongly on the size of the inner cavities of these macrocycles. New results have stimulated us to compile the synthetic entries and the complexations of pillar[6]arenes with large cylindric cavities that offer space for many different guest molecules. 1 Introduction 2 Preparation of Pillar[6]arenes 2.1 Pillar[6]arenes by Macrocyclization Reactions 2.2 Hydroxypillar[6]arenes through Ether Cleavage 2.3 Hydroxypillar[6]ar…

Pyridinium CompoundsChemistrySupramolecular chemistryGeneral MedicineAlkylationMetalvisual_artPolymer chemistryvisual_art.visual_art_mediumAlkoxy groupOrganic chemistryMoleculesense organsSelectivityEther cleavageChemInform
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Conformational and Tautomeric Control by Supramolecular Approach in Ureido-N-iso-propyl,N’-4-(3-pyridin-2-one)pyrimidine

2019

Ureido-N-iso-propyl,N&rsquo

PyrimidineStereochemistryMolecular ConformationSupramolecular chemistryPharmaceutical ScienceArticleCatalysisAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundIsomerismlcsh:Organic chemistryDrug DiscoveryPyridineUreaMoleculeMoietyPhysical and Theoretical ChemistryMolecular switchvetysidoksetintermolecular interactionsOrganic ChemistryTemperaturemolekyylithydrogen bondingTautomermolecular switchKineticstautomerismPyrimidineschemistryChemistry (miscellaneous)Proton NMRQuantum TheoryThermodynamicsMolecular MedicineProtonstautomeria
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Ferrochirality: a simple theoretical model of interacting, dynamically invertible, helical polymers, 2. Molecular field approach: supports and the de…

1995

Using a molecular field approach, the effect of interaction between reversibly invertible, helical polymers is investigated theoretically. The helices are modelled by nearest-neighbour statistical thermodynamics. If the interaction energy between two helices of common handedness is lower than that of oppositely handed ones, a critical temperature Tc exists, below which the system spontaneously must leave the racemic state, though there is no contact to any chiral centre or force. This is analogous to the second-order phase transition of ferromagnets. The critical point increases with molecular weight and optical persistence of the helices. At the critical point the system is highly sensitiv…

Quantitative Biology::BiomoleculesPhase transitionPolymers and PlasticsStereochemistryChemistryOrganic ChemistrySupramolecular chemistryInteraction energyCondensed Matter PhysicsInorganic ChemistryCritical point (thermodynamics)Chemical physicsLiquid crystalHelixMaterials ChemistryOptical rotationPhase diagramMacromolecular Theory and Simulations
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Degrees of freedom effect on fragmentation in tandem mass spectrometry of singly charged supramolecular aggregates of sodium sulfonates

2013

The characteristic collision energy (CCE) to obtain 50% fragmentation of positively and negatively single charged non-covalent clusters has been measured. CCE was found to increase linearly with the degrees of freedom (DoF) of the precursor ion, analogously to that observed for synthetic polymers. This suggests that fragmentation behavior (e.g. energy randomization) in covalent molecules and clusters are similar. Analysis of the slope of CCE with molecular size (DoF) indicates that activation energy of fragmentation of these clusters (loss of a monomer unit) is similar to that of the lowest energy fragmentation of protonated leucine-enkephalin. Positively and negatively charged aggregates b…

Quantitative Biology::BiomoleculesPhysics::Instrumentation and DetectorsChemistryAnalytical chemistrySupramolecular chemistryProtonationActivation energyIonchemistry.chemical_compoundMonomerFragmentation (mass spectrometry)Covalent bondMoleculeSpectroscopyJournal of Mass Spectrometry
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Microgel regions in dilute agarose solutions: the notion of non-gelling concentration, and the role of spinodal demixing

1991

Abstract Freely drifting microgel regions are found in aqueous solutions of agarose, a representative biostructural polysaccharide, at concentrations between 0.01% and 0.05% w/v when quenched from 100°C to lower temperature. The size of these domains depends on the quench temperature and agarose concentration. The results agree with recent findings on the role that fluctuations within or close to the instability region of solution have as the initial step towards the self-assembly of supramolecular structures, and throw a new light on the notion of the lowest solute concentration needed for gelation.

QuenchingSpinodalAqueous solutionChemistrySpinodal decompositionSupramolecular chemistryAnalytical chemistryGeneral Physics and AstronomyInstabilityLight scatteringchemistry.chemical_compoundChemical physicsAgarosePhysical and Theoretical ChemistryChemical Physics Letters
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Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning

2015

Halogen bonding, a noncovalent interaction possessing several unique features compared to the more familiar hydrogen bonding, is emerging as a powerful tool in functional materials design. Herein, we unambiguously show that one of these characteristic features, namely high directionality, renders halogen bonding the interaction of choice when developing azobenzene-containing supramolecular polymers for light-induced surface patterning. The study is conducted by using an extensive library of azobenzene molecules that differ only in terms of the bond-donor unit. We introduce a new tetrafluorophenol-containing azobenzene photoswitch capable of forming strong hydrogen bonds, and show that an io…

RELIEF GRATINGSDENSITY-FUNCTIONAL THEORY CALCULATIONSMaterials sciencePHOTOINDUCED BIREFRINGENCE116 Chemical sciencesta221Supramolecular chemistryPhotochemistrysupramolecular chemistryDENSITY-FUNCTIONAL THEORYchemistry.chemical_compoundMaterials ChemistryMoleculeTHERMAL-ISOMERIZATIONPOLARIZATION DEPENDENCECO-CRYSTALSLIQUID-CRYSTAL ORDERta218chemistry.chemical_classificationta214Halogen bondta114PhotoswitchHydrogen bondPolymers Halogen Bonding Supramolecular Chemistry Photoresponsive AzobenzeneGeneral Chemistryhydrogen bondingPOLYMER-AZOBENZENE COMPLEXESSupramolecular polymersSOLID-STATEchemistryAzobenzeneHALOGEN BONDINGHalogenlight-induced surface patterningSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTONIC APPLICATIONSPOLYMER-AZOBENZENE COMPLEXES; DENSITY-FUNCTIONAL THEORY; LIQUID-CRYSTAL ORDER; RELIEF GRATINGS; SOLID-STATE; PHOTOINDUCED BIREFRINGENCE; POLARIZATION DEPENDENCE; THERMAL-ISOMERIZATION; PHOTONIC APPLICATIONS; CO-CRYSTALSJournal of Materials Chemistry C
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Hydrogen-bonded liquid crystals with broad-range blue phases

2019

We report a modular supramolecular approach for the investigation of chirality induction in hydrogen-bonded liquid crystals. An exceptionally broad blue phase with a temperature range of 25 °C was found, which enabled its structural investigation by solid state 19F-NMR studies and allowed us to report order parameters of the blue phase I for the first time.

Range (particle radiation)Materials scienceHydrogenChemieSupramolecular chemistrySolid-statechemistry.chemical_element02 engineering and technologyGeneral ChemistryAtmospheric temperature range010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesLiquid Crystals Hydrogen Bonding Blue Phases Fluorine Supramolecular Chemistry0104 chemical sciencesCrystallographychemistryLiquid crystalPhase (matter)Materials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyChirality (chemistry)
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Ultrathin Organic Multilayer Films Via Salt Formation: Easy Access To Tailor-made Coatings In The Thickness Range Of 1 Nm To 500 Nm

2005

The state of the art technologies for the preparation of well defined ultrathin films in the submicron range are the Langmuir-Blodgett (LB) technique and self-assembly (SA) methods based on chemisorption [l]. Whereas the LBtechnique requires sophisticated apparatus and is generally limited to small film areas [2], the SA-methods are relatively simple [3,4], hut have not been employed for the preparation of films thicker than 8 layers ( 20nm) [4], probably due to the loss of chemical functionality. Our approach avoids these limits and extends the SA-concept by emploing salt formation as the driving force for the construction of multilayer supramolecular assemblies.

Range (particle radiation)Materials scienceOptical microscopeChemisorptionlawSupramolecular chemistryNanotechnologySelf-assemblyWell-definedSurface cleaningSalt formationlaw.invention[1990] Proceedings of the Twelfth Annual International Conference of the IEEE Engineering in Medicine and Biology Society
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