Search results for " Halogen Bonding"

showing 10 items of 10 documents

Superfluorinated ionic liquid crystals based on supramolecular, halogen-bonded anions

2016

Unconventional ionic liquid crystals in which the liquid crystallinity is enabled by halogen-bonded supramolecular anions [CnF2 n+1-I⋯I⋯I-CnF2 n+1]- are reported. The material system is unique in many ways, demonstrating for the first time 1) ionic, halogen-bonded liquid crystals, and 2) imidazolium-based ionic liquid crystals in which the occurrence of liquid crystallinity is not driven by the alkyl chains of the cation. Out of the ordinary: The high directionality of halogen bonds and the fluorophobic effect were exploited in the design and synthesis of a new family of unconventional superfluorinated ionic liquid crystals. The liquid crystallinity of the system is driven by halogen-bonded…

116 Chemical sciencesInorganic chemistry1600Supramolecular chemistryIonic bonding010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryCrystallinitychemistry.chemical_compoundLiquid crystal1503ta116Alkylchemistry.chemical_classificationHalogen bondionic liquid crystal010405 organic chemistryChemistryCommunicationChemistry (all)Self-assemblyGeneral MedicineGeneral Chemistryself-assemblyFluorophobic effect; Halogen bonding; Ionic liquid crystals; Self-assembly; Supramolecular chemistry; Chemistry (all); CatalysisCommunicationsfluorophobic effect0104 chemical sciencesCrystallographyhalogen bondingIonic liquidIonic liquid crystalsSettore CHIM/07 - Fondamenti Chimici Delle TecnologieFluorophobic effectSelf-assemblyHalogen bondingionic liquid crystalsSupramolecular chemistry
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Formation and distortion of iodidoantimonates(III): the first isolated [SbI6]3- octahedron

2017

The ability to intentionally construct, through different types of interactions, inorganic–organic hybrid materials with desired properties is the main goal of inorganic crystal engineering. The primary deformation, related to intrinsic interactions within inorganic substructure, and the secondary deformation, mainly caused by the hydrogen bond interactions, are both responsible for polyhedral distortions of halogenidoantimonates(III) with organic cations. The evolution of structural parameters, in particular the Sb—I secondary- and O/N/C—H...I hydrogen bonds, as a function of temperature assists in understanding the contribution of those two distortion factors to the irregularity of [SbI6]…

Coordination sphereTetrahydrate010405 organic chemistryChemistryHydrogen bondMetals and Alloys010402 general chemistryCrystal engineeringisolated [SbI6]3− octahedron01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyOctahedronDistortionpiperazine-1Materials ChemistryMoleculeWater of crystallization4-diium cationoctahedral distortion;hydrogen and halogen bondingiodidoantimonates(III)Acta Crystallographica Section B-Structural Science
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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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Halogen bonding stabilizes a cis-azobenzene derivative in the solid state : A crystallographic study

2017

Crystals oftrans- andcis-isomers of a fluorinated azobenzene derivative have been prepared and characterized by single-crystal X-ray diffraction. The presence of F atoms on the aromatic core of the azobenzene increases the lifetime of the metastablecis-isomer, allowing single crystals of thecis-azobenzene to be grown. Structural analysis on thecis-azobenzene, complemented with density functional theory calculations, highlights the active role of the halogen-bond contact (N...I synthon) in promoting the stabilization of thecis-isomer. The presence of a long aliphatic chain on the azobenzene unit induces a phase segregation that stabilizes the molecular arrangement for both thetrans- andcis-i…

Materials Chemistry2506 Metals and Alloys116 Chemical sciencesCrystal structure010402 general chemistryPhotochemistry01 natural sciencesazobenzene; halogen bonding; isomerization; Electronic Optical and Magnetic Materials; Atomic and Molecular Physics and Optics; 2506; Materials Chemistry2506 Metals and Alloysisomerizationchemistry.chemical_compoundPhase (matter)Atomic and Molecular PhysicsMaterials ChemistryElectronicOptical and Magnetic MaterialsHalogen bondta114010405 organic chemistryChemistrySynthonMetals and AlloysAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyazobenzeneAzobenzenehalogen bondingDensity functional theorySettore CHIM/07 - Fondamenti Chimici Delle Tecnologieand Optics2506IsomerizationDerivative (chemistry)
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Photoalignment and Surface-Relief-Grating Formation are Efficiently Combined in Low-Molecular-Weight Halogen-Bonded Complexes

2012

It is demonstrated that halogen bonding can be used to construct low-molecular-weight supramolecular complexes with unique light-responsive properties. In particular, halogen bonding drives the formation of a photoresponsive liquid-crystalline complex between a non-mesogenic halogen bond-donor molecule incorporating an azo group, and a non-mesogenic alkoxystilbazole moiety, acting as a halogen bond-acceptor. Upon irradiation with polarized light, the complex exhibits a high degree of photoinduced anisotropy (order parameter of molecular alignment > 0.5). Moreover, efficient photoinduced surface-relief-grating (SRG) formation occurs upon irradiation with a light interference pattern, with…

Materials scienceLightSurface Propertiesta221Supramolecular chemistryPhotochemistrysupramolecular complexeschemistry.chemical_compoundHalogensliquid crystalsLiquid crystalMaterials TestingMoietyMoleculeGeneral Materials Scienceliquid crystalta218Halogen bondta214Azobenzeneta114Mechanical Engineeringself-assemblyMolecular WeightRefractometryazobenzeneAzobenzenechemistryMechanics of Materialshalogen bondingHalogenazobenzene; halogen bonding; liquid crystals; self-assembly; supramolecular complexesSelf-assemblySettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesurface relief gratings
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Surface-relief gratings in halogen-bonded polymer-azobenzene complexes A concentration-dependence study

2017

In recent years, supramolecular complexes comprising a poly(4-vinylpyridine) backbone and azobenzene-based halogen bond donors have emerged as a promising class of materials for the inscription of light-induced surface-relief gratings (SRGs). The studies up to date have focused on building supramolecular hierarchies, i.e., optimizing the polymer–azobenzene noncovalent interaction for efficient surface patterning. They have been conducted using systems with relatively low azobenzene content, and little is known about the concentration dependence of SRG formation in halogen-bonded polymer–azobenzene complexes. Herein, we bridge this gap, and study the concentration dependence of SRG formation…

Polymers116 Chemical sciencesPharmaceutical Science02 engineering and technologyPhotoresponsiveMicroscopy Atomic Force01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundHalogenslawDrug DiscoverySupramolecularPolymerchemistry.chemical_classificationHalogen bondMolecular StructureAzobenzenePolymer021001 nanoscience & nanotechnologyAzobenzeneChemistry (miscellaneous)HalogenHalogenMolecular MedicineHalogen bonding0210 nano-technologyMaterials scienceSurface PropertiesChemieSupramolecular chemistry010402 general chemistrySurface-relief gratingArticleAzo Compoundlcsh:QD241-441lcsh:Organic chemistryOptical microscopeMoleculePhysical and Theoretical ChemistryThin filmta114Organic Chemistry0104 chemical sciencesCrystallographychemistrysurface-relief grating; azobenzene; halogen bonding; supramolecular; photoresponsiveSettore CHIM/07 - Fondamenti Chimici Delle TecnologieAzo CompoundsMOLECULES
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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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Halogen-bonded photoresponsive materials

2015

The aim of the present review is to illustrate to the reader the state of the art on the construction of supramolecular azobenzene-containing materials formed by halogen bonding. These materials include several examples of polymeric, liquid crystalline or crystalline species whose performances are either superior to the corresponding performances of their hydrogen-bonded analogues or simply distinctive of the halogen-bonded species. submittedVersion Peer reviewed

chemistry.chemical_classificationHalogen bondAzobenzene; Halogen bonding; Liquid crystals; Photoresponsive materials; PolymersAzobenzeneLiquid crystallinePolymersLiquid crystals116 Chemical sciencesSupramolecular chemistryPolymerchemistry.chemical_compoundchemistryAzobenzeneLiquid crystalPhotoresponsive materialLiquid crystalPolymer chemistryHalogenSettore CHIM/07 - Fondamenti Chimici Delle TecnologieHalogen bondingta116Photoresponsive materials
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Photoresponsive ionic liquid crystals assembled: Via halogen bond: En route towards light-controllable ion transporters

2017

We demonstrate that halogen bonding (XB) can offer a novel approach for the construction of photoresponsive ionic liquid crystals. In particular, we assembled two new supramolecular complexes based on 1-ethyl-3-methylimidazolium iodides and azobenzene derivatives containing an iodotetrafluoro-benzene ring as XB donor, where the iodide anion acted as an XB acceptor. DSC and X-ray diffraction analyses revealed that the preferred stoichiometry between the XB donors and acceptors is 2 : 1, and that the iodide anions act as bidentate XB-acceptors, binding two azobenzene derivatives. Due to the high directionality of the XB, calamitic superanions are obtained, while the segregation occurring betw…

chemistry.chemical_classificationHalogen bondta114ChemistryInorganic chemistryIodideSupramolecular chemistryIonic bonding02 engineering and technologySupramolecular Chemistry Liquid Crystals Halogen Bonding Photoresponsive010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptor0104 chemical sciencesCrystallographychemistry.chemical_compoundAzobenzeneIonic liquidMoleculeSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistry0210 nano-technology
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Halogen bonding enhances nonlinear optical response in poled supramolecular polymers

2015

We demonstrate that halogen bonding strongly enhances the nonlinear optical response of poled supramolecular polymer systems. We compare three nonlinear optical chromophores with similar electronic structures but different bond-donating units, and show that both the type and the strength of the noncovalent interaction between the chromophores and the polymer matrix play their own distinctive roles in the optical nonlinearity of the systems. acceptedVersion Peer reviewed

chemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesMaterials scienceHalogen bond116 Chemical sciencesGeneral ChemistryPolymerChromophorePolymers Supramolecular Chemistry Halogen Bonding Nonlinear Optical ResponseHalogen bonding; NLO; supramolecular polymers114 Physical sciencesSupramolecular polymersCondensed Matter::Soft Condensed MatterOptical nonlinearityNonlinear opticalchemistryChemical physicsPolymer chemistryMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysics::Chemical Physics
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