Search results for " Supramolecular chemistry"

showing 10 items of 29 documents

Improving the mesomorphic behaviour of supramolecular liquid crystals by resonance-assisted hydrogen bonding

2019

A systematic structure-property relationship study on hydrogen-bonded liquid crystals was performed, revealing the impact of resonance-assisted hydrogen bonds (RAHBs) on the self-assembling behavior of the supramolecular architecture. The creation of a six-membered intramolecular hydrogen-bonded ring acts as a counterpart to the self-organization between hydrogen bond donators and acceptors and determines thus the suprastructure. Variation of the hydrogen-bonding pattern allowed us to significantly improve the temperature range of the reported liquid crystalline assemblies.

Materials scienceLiquid crystallineHydrogen bondChemieSupramolecular chemistry02 engineering and technologyGeneral ChemistryAtmospheric temperature range010402 general chemistry021001 nanoscience & nanotechnologyRing (chemistry)Resonance (chemistry)01 natural sciences0104 chemical sciencesCrystallographyLiquid Crystals Hydrogen Bonding Structure-Property Supramolecular Chemistry intramolecularLiquid crystalIntramolecular forceMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyJournal of Materials Chemistry C
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Molecular Rearrangement of an Aza-Scorpiand Macrocycle Induced by pH: A Computational Study †

2016

Rearrangements and their control are a hot topic in supramolecular chemistry due to the possibilities that these phenomena open in the design of synthetic receptors and molecular machines. Macrocycle aza-scorpiands constitute an interesting system that can reorganize their spatial structure depending on pH variations or the presence of metal cations. In this study, the relative stabilities of these conformations were predicted computationally by semi-empirical and density functional theory approximations, and the reorganization from closed to open conformations was simulated by using the Monte Carlo multiple minimum method Financial support by the Spanish Ministerio de Economía y Competitiv…

Models MolecularMontecarlo Mètode deMonte Carlo method01 natural sciencessupramolecular chemistryMonte Carlo Multiple Minimumlcsh:ChemistryComputational chemistryaza-scorpiandsMolecular rearrangementpH controlled; supramolecular chemistry; synthetic receptors; aza-scorpiands; semi-empirical; Density Functional Theory; Monte Carlo Multiple Minimumlcsh:QH301-705.5semi-empiricalSpectroscopyDensity Functional TheoryDensity functionalsSpatial structureChemistryGeneral MedicineHydrogen-Ion ConcentrationMolecular machineComputer Science ApplicationsMonte Carlo methodpH controlledvisual_artsynthetic receptorsvisual_art.visual_art_mediumDensity functional theoryMonte Carlo MethodMacrocyclic CompoundsSupramolecular chemistry010402 general chemistryQuímica supramolecularCatalysisArticleInorganic ChemistryMetalQuantitative Biology::Subcellular ProcessesPhysical and Theoretical ChemistryMolecular BiologyAza CompoundsFuncional de densitat Teoria del010405 organic chemistryOrganic ChemistryComputational Biology0104 chemical scienceslcsh:Biology (General)lcsh:QD1-999Synthetic ReceptorsQuantum TheorySupramolecular chemistryInternational Journal of Molecular Sciences
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Selectivity of cyclodextrins as a parameter to tune the formation of pseudorotaxanes and micelles supramolecular assemblies. A systematic SANS study

2011

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively. We studied the formation of polypseudorotaxanes formed with cyclodextrins (CDs) threading a copolymer chain that forms self-assembled structures in water. The size of the CD cavity was chosen such that it is block selective with respect to the formation of inclusion complexes and therefore in terms of altering the structure of the copolymer self-assemblies in a systematic fashio…

Neutron scattering supramolecular chemistry cyclodextrin pseudorotaxaneschemistry.chemical_classificationMaterials scienceCyclodextrinSupramolecular chemistry02 engineering and technologyGeneral ChemistryNeutron scattering010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSmall-angle neutron scatteringMicelle0104 chemical sciencesCrystallographychemistryCopolymerddc:5300210 nano-technologySelectivityDissolutionSettore CHIM/02 - Chimica Fisica
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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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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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Organic Salts as Tectons for Self-assembly Processes in Solution

2022

The literature, covering the last decade, about the self-assembly processes of organic salts in conventional solvents was analyzed. In particular, data reported about imidazolium and ammonium salts have been considered. The analysis shows that these processes are highly determined by structural features of the salts. Indeed, besides the nature of the cationic head, features of the alkyl chain borne on the cation structure and its possible functionalization, as well as the nature of the anion play a pivotal role. These factors determine not only the nature of the solvent in which the process occurs but also the nature of the self-assembly mechanism. Consequently, the structure tunability of …

Settore CHIM/06 - Chimica OrganicaSelf assembly supramolecular chemistry electrostatic interactions.
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Walking through Soft Materials to Join Supramolecular Gels: An Overview about the Properties and Applications

The class of soft materials includes a large variety of species arising from self-assembly processes and held by non-covalent interactions. This confers peculiar features, allowing applications in very different fields.1 Among soft materials, supramolecular gel phases have aroused a surge of interest.2 These materials combine properties of liquid phase with the ones of a semi-solid network and the large number of gelator/solvent combinations can offer answer to issues of different nature.3 This lecture will show on overview about the obtainment and characterization of gel phases, in the attempt to understand the relationship working between gelator and solvent nature and gel phase propertie…

Settore CHIM/06 - Chimica OrganicaSupramolecular gels Ionogels Supramolecular chemistry
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A preliminary study on anion binding ability of geminal diimidazolium salts

Settore CHIM/06 - Chimica Organicaimidazolium salts anion recognition supramolecular chemistry
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ortho -Fluorination of azophenols increases the mesophase stability of photoresponsive hydrogen-bonded liquid crystals

2018

Photoresponsive liquid crystals (LCs) whose alignment can be controlled with UV-Visible light are appealing for a range of photonic applications. From the perspective of exploring the interplay between the light response and the self-assembly of the molecular components, supramolecular liquid crystals are of particular interest. They allow elaborating the structure-property relationships that govern the optical performance of LC materials by subtle variation of the chemical structures of the building blocks. Herein we present a supramolecular system comprising azophenols and stilbazoles as hydrogen-bond donors and acceptors, respectively, and show that ortho-fluorination of the azophenol dr…

Solid-state chemistryMaterials scienceHydrogen116 Chemical sciencesChemieSupramolecular chemistrychemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesLiquid crystalMaterials ChemistryThermal stabilityLight responsebusiness.industryFluorine Liquid Crystals Supramolecular Chemistry Hydrogen bonding PhotoresponsiveMesophaseGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotonics0210 nano-technologybusinessJournal of Materials Chemistry C
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