Search results for "Halogen bonding"

showing 10 items of 35 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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Dissecting the packing forces in mixed perfluorocarbon/aromatic co-crystals

2021

We carried out a systematic evaluation of the packing forces in co-crystals featuring monoiodo- and diiodo-perfluoroalkanes and 1,2,4-oxadiazoles through single crystal X-ray diffraction and theoretical analysis. The molecules assemble via a combination of halogen bonding and specific dispersive interactions involving the perfluorinated units. We quantitatively elucidated the nature and strength of such interactions through solid-state calculations and Hirshfeld surface analysis. One of the co-crystals, formed by two monoiodoperfluorodecane molecules, the longest perfluorinated chain ever solved at the atomic level, allowed us to fully highlight the role of fluorous interactions.

DiffractionMaterials scienceHalogen bondperfluorocarbonSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCondensed Matter PhysicsmodellingCrystallographyChain (algebraic topology)crystal engineeringMoleculehalogen bondGeneral Materials Sciencehalogen bonding supramolecular interactions crystal packingSingle crystalCrystEngComm
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Halogen and Hydrogen Bonded Complexes of 5-Iodouracil

2013

Three derivatives of 5-iodouracil were prepared, and their complexation properties, supplemented by 5-iodouracil under the same conditions, were studied with and without halogen bond acceptors in N,N-dimethylformamide, N,N-diethylformamide, N-methylformamide, formamide, dimethylsulfoxide, and water. The intermolecular halogen and hydrogen bonding interactions observed in the solid state were investigated using single crystal X-ray diffraction and quantum chemical calculations, and the acquired data were contrasted with bonding interactions previously reported for 5-iodouracil in the Cambridge Structural Database. It was found that the polarized iodine atom and the amidic NH functionality ac…

FormamideHalogen bondvetysidoksetHydrogenHydrogen bondInorganic chemistryIntermolecular forcechemistry.chemical_element5-jodourasiili5-iodouracilGeneral ChemistryCrystal structureCondensed Matter Physicshydrogen bondingCrystallographychemistry.chemical_compoundchemistryhalogen bondingHalogenhalogeenisidoksetGeneral Materials ScienceSingle crystalta116
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Halogen Bonding beyond Crystals in Materials Science

2019

Halogen bonding has recently gained well deserved attention in present-day research for its importance in many fields of supramolecular science and crystal engineering. Although generally overlooked in comprehensive studies in the past, halogen bonding has become an important tool also in the field of materials science. An increased number of scientific reports are published every year where halogen bonding is exploited in soft materials rather than in crystal engineering. Here, we focus on a description of the most exciting contemporary developments in the field of halogen-bonded functional soft materials, assembled using the guiding principles of crystal engineering. We give a particular …

Halogen BondingHalogen bondMaterials science010304 chemical physicsChemieNanotechnology010402 general chemistryCrystal engineering01 natural sciencesSoft materialsSupramolecular Chemistry0104 chemical sciencesSurfaces Coatings and Films0103 physical sciencesMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryLiquid CrystalPolymerCrystals Gel
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Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors

2021

Abstract Neutral halogen‐bonded O−I−N complexes were prepared from in situ formed carbonyl hypoiodites and aromatic organic bases. The carbonyl hypoiodites have a strongly polarized iodine atom with larger σ‐holes than any known uncharged halogen bond donor. Modulating the Lewis basicity of the selected pyridine derivatives and carboxylates leads to halogen‐bonded complexes where the classical O−I⋅⋅⋅N halogen bond transforms more into a halogen‐bonded COO−⋅⋅⋅I−N+ ion‐pair (salt) with an asymmetric O−I−N moiety. X‐ray analyses, NMR studies, and calculations reveal the halogen bonding geometries of the carbonyl hypoiodite‐based O−I−N complexes, confirming that in the solid‐state the iodine at…

Halogen Bondingpyridineinorganic chemicalsHalogen bondOrganic basehalogeenitCommunicationSupramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyGeneral MedicinehypoioditeMedicinal chemistryCatalysisCommunicationssupramolecular chemistrychemistry.chemical_compoundkemialliset sidoksetNMR spectroscopychemistryPyridineTrifluoroacetic acidsupramolekulaarinen kemiaMoietyCarboxylateAngewandte Chemie
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Fine-tuning halogen bonding properties of diiodine through halogen–halogen charge transfer – extended [Ru(2,2′-bipyridine)(CO)2X2]·I2 systems (X = Cl…

2016

The current paper introduces the use of carbonyl containing ruthenium complexes, [Ru(bpy)(CO)2X2] (X = Cl, Br, I), as halogen bond acceptors for a I2 halogen bond donor. In all structures, the metal coordinated halogenido ligand acts as the actual halogen bond acceptor. Diiodine, I2, molecules are connected to the metal complexes through both ends of the molecule forming bridges between the complexes. Due to the charge transfer from Ru–X to I2, formation of the first Ru–X⋯I2 contact tends to generate a negative charge on I2 and redistribute the electron density anisotropically. If the initial Ru–X⋯IA–IB interaction causes a notable change in the electron density of I2, the increased negativ…

Halogen bond010405 organic chemistryChemistryLigandchemistry.chemical_elementCharge densityGeneral Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesAcceptor22'-Bipyridine0104 chemical sciencesRutheniumCrystallographychemistry.chemical_compoundhalogen bondingHalogenruthenium complexesMoleculeGeneral Materials Scienceta116CrystEngComm
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The H2C(X)–X•••X– (X = Cl, Br) Halogen Bonding of Dihalomethanes

2017

The dihalomethane–halide H2C(X)–X···X– (X = Cl, Br) halogen bonding was detected in a series of the cis-[PdX(CNCy){C(NHCy)═NHC6H2Me2NH2}]X•CH2X2 (X = Cl, Br) associates by single-crystal XRD followed by DFT calculations. Although ESP calculations demonstrated that the σ-hole of dichloromethane is the smallest among all halomethane solvents (the maximum electrostatic potential is only 2.6 kcal/mol), the theoretical DFT calculations followed by Bader’s QTAIM analysis (M06/DZP-DKH level of theory) confirmed the H2C(X)–X···X– halogen bond in both the solid-state and gas-phase optimized geometries. The estimated bonding energy in H2C(X)–X···X– is in the 1.9–2.8 kcal/mol range.

Halogen bond010405 organic chemistryHalomethaneGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesdihalomethanes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryComputational chemistryhalogen bondingGeneral Materials ScienceBond energyta116DichloromethaneCrystal Growth and Design
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The subtle balance of weak supramolecular interactions: The hierarchy of halogen and hydrogen bonds in haloanilinium and halopyridinium salts

2010

The series of haloanilinium and halopyridinium salts: 4-IPhNH3Cl (1), 4-IPhNH3Br (5), 4-IPhNH3H2PO4 (6), 4-ClPhNH3H2PO4 (8), 3-IPyBnCl (9), 3-IPyHCl (10) and 3-IPyH-5NIPA (3-iodopyridinium 5-nitroisophthalate, 13), where hydrogen or/and halogen bonding represents the most relevant non-covalent interactions, has been prepared and characterized by single crystal X-ray diffraction. This series was further complemented by extracting some relevant crystal structures: 4-BrPhNH3Cl (2, CCDC ref. code TAWRAL), 4-ClPhNH3Cl (3, CURGOL), 4-FPhNH3Cl (4, ANLCLA), 4-BrPhNH3H2PO4, (7, UGISEI), 3-BrPyHCl, (11, CIHBAX) and 3-ClPyHCl, (12, VOQMUJ) from Cambridge Structural Database for sake of comparison. Bas…

Halogen bondHydrogenChemistryHydrogen bondOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementCrystal structurehydrogen bondingCrystal engineeringFull Research Papersupramolecular chemistrylcsh:QD241-441ChemistryCrystallographylcsh:Organic chemistrycrystal engineeringhalogen bondingHalogenweak interactionslcsh:Qlcsh:ScienceSingle crystalBeilstein Journal of Organic Chemistry
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NI halogen bonding supported stabilization of a discrete pseudo-linear [I12]2− polyiodide

2015

Two different dicationic N-donors, based on the DABCO diamine, have been studied as templates for polyiodides. The results present a new strategy for polyiodide stabilization, which involves both N⋯I halogen bonding and cation–anion interactions. This is highlighted by the self-assembly of an unprecedented discrete pseudo-linear dodecaiodide species.

Halogen bondInorganic chemistryGeneral ChemistryDABCOCondensed Matter Physicschemistry.chemical_compoundPolyiodideTemplatechemistryhalogen bondingDiaminePolymer chemistryGeneral Materials Scienceta116CrystEngComm
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