0000000000310152

AUTHOR

Valentina Dichiarante

0000-0002-2977-5833

showing 9 related works from this author

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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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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Supramolecular control of liquid crystals by doping with halogen-bonding dyes

2017

Introducing photochromic or polymeric dopants into nematic liquid crystals is a well-established method to create stimuli-responsive photonic materials with the ability to "control light with light". Herein, we demonstrate a new material design concept by showing that specific supramolecular interactions between the host liquid crystal and the guest dopants enhance the optical performance of the doped liquid crystals. By varying the type and strength of the dopant-host interaction, the phase-transition temperature, the order parameter of the guest molecules, and the diffraction signal in response to interference irradiation, can be accurately engineered. Our concept points out the potential…

Materials scienceGeneral Chemical EngineeringHalogen Bonding Polymers Liquid Crystals Photoresponsive Materials Supramolecular Chemistry116 Chemical sciencesSupramolecular chemistryphotonicsPhysics::OpticsNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesPhotonic metamaterialPhotochromismliquid crystalsLiquid crystalCondensed Matter::Superconductivitydye-doped liquid crystalsta116ta215Halogen bondDopantbusiness.industryDopingGeneral Chemistry021001 nanoscience & nanotechnologysupramolecular interactions0104 chemical sciencesCondensed Matter::Soft Condensed Matterhalogen bondingOptoelectronicsSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotonics0210 nano-technologybusinessRSC Advances
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CCDC 1535157: Experimental Crystal Structure Determination

2017

Related Article: Jaana Vapaavuori, Antti Siiskonen, Valentina Dichiarante, Alessandra Forni, Marco Saccone, Tullio Pilati, Christian Pellerin, Atsushi Shishido, Pierangelo Metrangolo, Arri Priimagi|2017|RSC Advances|7|40237|doi:10.1039/C7RA06397K

Space GroupCrystallographyCrystal System4'-pentyl[11'-biphenyl]-4-carbonitrile NN-dimethyl-4-[(2356-tetrafluoro-4-iodophenyl)diazenyl]anilineCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1541305: Experimental Crystal Structure Determination

2017

Related Article: Marco Saccone, Francisco Fernandez Palacio, Gabriella Cavallo, Valentina Dichiarante, Matti Virkki, Giancarlo Terraneo, Arri Priimagi, Pierangelo Metrangolo|2017|Faraday Discuss.|203|407|doi:10.1039/C7FD00120G

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters3-methyl-1-octyl-1H-imidazol-3-ium bis(NN-dimethyl-4-((2356-tetrafluoro-4-iodophenyl)diazenyl)aniline) iodideExperimental 3D Coordinates
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CCDC 1541306: Experimental Crystal Structure Determination

2017

Related Article: Marco Saccone, Francisco Fernandez Palacio, Gabriella Cavallo, Valentina Dichiarante, Matti Virkki, Giancarlo Terraneo, Arri Priimagi, Pierangelo Metrangolo|2017|Faraday Discuss.|203|407|doi:10.1039/C7FD00120G

Space GroupCrystallographyCrystal System1-dodecyl-3-methyl-1H-imidazol-3-ium bis(1-(4-(dodecyloxy)phenyl)-2-(2356-tetrafluoro-4-iodophenyl)diazene) iodideCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1025655: Experimental Crystal Structure Determination

2014

Related Article: Marco Saccone, Valentina Dichiarante, Alessandra Forni, Alexis Goulet-Hanssens, Gabriella Cavallo, Jaana Vapaavuori, Giancarlo Terraneo, Christopher J. Barrett, Giuseppe Resnati, Pierangelo Metrangolo, Arri Priimagi|2015|J.Mater.Chem.C|3|759|doi:10.1039/C4TC02315C

Space GroupCrystallographybis(4-((4-(dimethylamino)phenyl)diazenyl)-2356-tetrafluorophenol) 44'-ethene-12-diyldipyridineCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1025656: Experimental Crystal Structure Determination

2014

Related Article: Marco Saccone, Valentina Dichiarante, Alessandra Forni, Alexis Goulet-Hanssens, Gabriella Cavallo, Jaana Vapaavuori, Giancarlo Terraneo, Christopher J. Barrett, Giuseppe Resnati, Pierangelo Metrangolo, Arri Priimagi|2015|J.Mater.Chem.C|3|759|doi:10.1039/C4TC02315C

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(4-((4-(iodoethynyl)phenyl)diazenyl)-NN-dimethylaniline) 44'-ethene-12-diyldipyridineExperimental 3D Coordinates
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