Search results for "ta116"

showing 10 items of 942 documents

The Effect of Halogen Bonding on the Packing of Bromine Substituted Pyridine and Benzyl Functionalized Resorcinarene Tetrapodands in the Solid State

2012

The synthesis and characterization of new bromine-substituted pyridine and benzyl functionalized tetramethoxy resorcinarene tetrapodands are described and their solid-state structural properties and interactions were studied by single crystal X-ray crystallography. Three different crystal structures were obtained for the pyridine derivative and one for the benzyl derivative, which revealed that the interactions of the bromine substituent have an explicit effect on the crystal packing of the resorcinarene molecules. One of the structures obtained had very interesting halogen–halogen interactions with the same geometry as is generally found for compounds used in nonlinear optical studies.

Halogen bondSubstituentGeneral ChemistryCrystal structureResorcinareneCondensed Matter Physicschemistry.chemical_compoundchemistryPyridinePolymer chemistryMoleculeOrganic chemistryGeneral Materials ScienceSingle crystalta116Derivative (chemistry)CrystEngComm
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Halogen bonding—a key step in charge recombination of the dye-sensitized solar cell

2011

The halogen bonding between [Ru(dcbpy)(2)(SCN)(2)] dye and I(2) molecule has been studied. The ruthenium complex forms a stable [Ru(dcbpy)(2)(SCN)(2)]···I(2)·4(CH(3)OH) adduct via S···I interaction between the thiocyanate ligand and the I(2) molecule. The adduct can be seen as a model for one of the key intermediates in the regeneration cycle of the oxidized dye by the I(-)/I(3)(-) electrolyte in dye sensitized solar cells.

Halogen bondThiocyanateLigandMetals and Alloyschemistry.chemical_elementGeneral ChemistryElectrolytePhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductRutheniumchemistry.chemical_compoundDye-sensitized solar cellchemistryMaterials ChemistryCeramics and CompositesMoleculeta116Chemical Communications
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Modification of the supramolecular structure of [(thione)IY] (Y = Cl, Br) systems by cooperation of strong halogen bonds and hydrogen bonds

2015

Four interhalogen complexes of heterocyclic thione ligands N-methylbenzothiazole-2-thione (mbtt) and 2(3)H-benzothiazole-thione (btt) with strong and tunable S⋯I halogen bonds were synthesized and characterized by X-ray single crystal diffraction. The study of the strength and nature of the interactions was supported by computational analysis using the Quantum Theory of Atoms in Molecules (QTAIM). Halogen bond and hydrogen bond directed self-assemblies of thione compounds were efficiently modified by the changes in the halogen bond donor and acceptor structures. In structures [(mbtt)ICl] (1) and [(mbtt)IBr] (2) the interplay of halogen bonds and hydrogen bonds between the thione hydrogens a…

Halogen bondsynthesisHydrogenHydrogen bondhalogen bondsInorganic chemistryAtoms in moleculesSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsAcceptorinterhalogen complexesCrystallographychemistryhydrogen bondsHalogenGeneral Materials Scienceta116InterhalogenCrystEngComm
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Synthesis of Highly Functionalized Fluorinated Cispentacin Derivatives

2012

Fluorinated highly functionalized cispentacin derivatives were synthetised starting from an unsaturated bicyclic b-lactam through C¼C bond functionalization via the dipolar cycloaddition of a nitrile oxide, isoxazoline opening, and fluorination by OH/F exchange.

HalogenationBicyclic moleculeNitrileOxideOxidesBioengineeringCispentacinGeneral ChemistryGeneral Medicinebeta-LactamsBiochemistryCycloadditionchemistry.chemical_compoundchemistryCyclizationNitrilesMolecular MedicineSurface modificationOrganic chemistryCycloleucineta116Molecular BiologyChemistry & Biodiversity
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Guest Induced Strong Cooperative One- and Two-Step Spin Transitions in Highly Porous Iron(II) Hofmann-Type Metal-Organic Frameworks.

2017

[EN] The synthesis, crystal structure, magnetic, calorimetric, and Mo¿ ssbauer studies of a series of new Hofmann-type spin crossover (SCO) metal¿organic frameworks (MOFs) is reported. The new SCO-MOFs arise from self-assembly of FeII, bis(4-pyridyl)butadiyne (bpb), and [Ag(CN)2] ¿ or [MII(CN)4] 2¿ (MII = Ni, Pd). Interpenetration of four identical 3D networks with ¿-Po topology are obtained for {Fe(bpb)[AgI (CN)2]2} due to the length of the rod-like bismonodentate bpb and [Ag(CN)2] ¿ ligands. The four networks are tightly packed and organized in two subsets orthogonally interpenetrated, while the networks in each subset display parallel interpenetration. This nonporous material undergoes a…

Hofmann-type coordination polymers010405 organic chemistryStereochemistryCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryNitrobenzenechemistry.chemical_compoundCrystallographychemistrySpin crossoverFISICA APLICADAHighly porousMössbauer spectroscopyMoleculePhysical and Theoretical ChemistrySpin (physics)Porous mediumta116Inorganic chemistry
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Dual Hydrogen Bond - Enamine Catalysis Enables a Direct Enantioselective Three-Component Domino Reaction

2011

A dual system, composed of an enantioselective enamine catalyst and a multiple-hydrogen-bond catalyst achieves the three-component enantioselective aldehyde—nitroalkene—aldehyde domino reaction using either two similar or two different aldehydes.

Hydrogen bond catalysisComponent (thermodynamics)Hydrogen bondChemistryEnantioselective synthesisGeneral MedicineGeneral ChemistryCatalysisCatalysisEnaminechemistry.chemical_compoundCascade reactionOrganocatalysisOrganic chemistryta116Angewandte Chemie Intermational Edition
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NMR crystallography of 2-Acylamino-6-[1H]pyridones: solid state NMR, GIPAW computational, and single crystal X-ray diffraction studies

2011

Abstract 2-Acylamino-6-[1H]-pyridones [acyl = RCO, where R = methyl (1), ethyl (2), iso-propyl (3), tert-butyl (4), and 1-adamantyl (5)] have been synthesized and characterized by NMR spectroscopy. From three congeners, 2, 3 and 5, also single crystal X-ray structures have been solved. For these derivatives GIPAW calculations acts as a “bridge” between solid-state NMR data and calculated chemical shifts based on X-ray determined geometry. In crystals all three compounds exist as pyridone tautomers possessing similar six-membered ring structure stabilized by intramolecular C O⋯HN hydrogen bond. Theoretical GIPAW calculated and experimental 13C and 15N CPMAS NMR shifts are in excellent agreem…

Hydrogen bondCarbon-13 NMR satelliteChemistryChemical shiftOrganic ChemistryNuclear magnetic resonance spectroscopyNuclear magnetic resonance crystallographyTautomerAnalytical ChemistryInorganic ChemistryCrystallographySolid-state nuclear magnetic resonanceIntramolecular forceta116SpectroscopyJournal of Molecular Structure
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A second monoclinic polymorph of 2-(3,5-dimethyl-1H-pyrazol-1-yl)-2-hy-droxy-imino-N'-[1-(pyridin-2-yl)ethyl-idene]acetohydrazide.

2013

The title compound, C14H16N6O2, is a second monoclinic polymorph of 2-[1-(3,5-dimeth­yl)pyrazol­yl]-2-hy­droxy­imino-N′-[1-(2-pyrid­yl)ethyl­idene] acetohydrazide, with two crystallographically independent mol­ecules per asymmetric unit. The non-planar mol­ecules are chemically equal having similar geometric parameters. The previously reported polymorph [Plutenko et al. (2012 ▶). Acta Cryst. E68, o3281] was described in space group Cc (Z = 4). The oxime group and the O atom of the amide group are anti with respect to the C—C bond. In the crystal, mol­ecules are connected by N—H⋯N hydrogen bonds into zigzag chains extending along the b axis.

Hydrogen bondGeneral ChemistryCondensed Matter PhysicsOximeBioinformaticsMedicinal chemistryOrganic Paperschemistry.chemical_compoundchemistryGroup (periodic table)AmideGeneral Materials Scienceta116Monoclinic crystal systemActa crystallographica. Section E, Structure reports online
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Concerted halogen and hydrogen bonding in [RuI2(H2dcbpy)(CO)2]···I2···(CH3OH)···I2···[RuI2(H2dcbpy)(CO)2].

2011

A new type of concerted halogen bond-hydrogen bond interaction was found in the solid state structure of [RuI(2)(H(2)dcbpy)(CO)(2)]···I(2)···(MeOH)···I(2)···[RuI(2)(H(2)dcbpy)(CO)(2)]. The iodine atoms of the two I(2) molecules interact simultaneously with each other and with the OH group of methanol of crystallization. The interaction was characterized by single crystal X-ray measurements and by computational charge density analysis based on DFT calculations.

Hydrogen bondMetals and AlloysCharge densityGeneral ChemistrySolid state structureCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundCrystallographychemistryComputational chemistrylawHalogenMaterials ChemistryCeramics and CompositesMoleculeMethanolCrystallizationSingle crystalta116Chemical communications (Cambridge, England)
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Synthesis of tetrahalide dianions directed by crystal engineering

2015

CrystEngComm 17(35), 6641-6645(2015). doi:10.1039/C5CE01288K

Hydrogen bondStereochemistryChemistryRational designCharge (physics)General ChemistryCrystal structureCondensed Matter PhysicsCrystal engineering540crystal engineeringChemical physicsHalogenddc:540tetrahalide dianionsGeneral Materials Scienceta116
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