Search results for "Dimer"

showing 10 items of 558 documents

Influences of Chemical Functionalities on Crystal Structures and Electrochemical Properties of Dihydro-benzoxazine Dimer Derivatives

2021

Dihydro-1,3,2H-benzoxazine dimer derivatives or dihydro-benzoxazine dimers are a class of compounds typically prepared by ring-opening reactions between dihydro-benzoxazines and phenols. Dihydro-benzoxazine dimers act as chelating agents for several transition and rare-earth cations. To better understand the chelating properties, it is necessary to examine their structural features and electrochemical characteristics thoroughly. However, the electrochemical properties of dihydro-benzoxazine dimers have not been tremendously examined. Herein, eight derivatives of dihydro-benzoxazine dimers possessing different substituents on the benzene ring and the tertiary-amine nitrogen were synthesized …

crystal structureCrystallographyHydrogen bondGeneral Chemical EngineeringDimerHirshfeld surfaceIntermolecular forceCrystal structureCondensed Matter PhysicsRedoxInorganic ChemistryCrystalelectrochemical propertychemistry.chemical_compoundCrystallographychemistryQD901-999General Materials SciencebenzoxazineCyclic voltammetryMethyleneCrystals
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Crystal structure and Hirshfeld surface analysis of 1-(2,4-dichlorobenzyl)-5-methyl-N-(thiophene-2-sulfonyl)-1H-pyrazole-3-carboxamide

2018

In the title compound, C16H13Cl2N3O3S2, the thiophene ring is disordered in a 0.762 (3):0.238 (3) ratio by an approximate 180° rotation of the ring around the S—C bond linking the ring to the sulfonyl unit. The dichlorobenzene group is also disordered over two sets of sites with the same occupancy ratio. The molecular conformation is stabilized by intramolecular C—H...Cl and C—H...N hydrogen bonds, forming rings with graph-set notation S(5). In the crystal, pairs of molecules are linked by N—H...O and C—H...O hydrogen bonds, forming inversion dimers with graph-set notation R 2 2(8) and R 1 2(11), which are connected by C—H...O hydrogen-bonding interactions into ribbons parallel to (100). Th…

crystal structureDimer1H-pyrazole ringStackingThio-Crystal structurePyrazole010403 inorganic & nuclear chemistryRing (chemistry)01 natural scienceslcsh:Chemistrychemistry.chemical_compoundthiophene ringGeneral Materials ScienceSulfonylchemistry.chemical_classification010405 organic chemistryHydrogen bondChemistrydisorderGeneral ChemistrydimerCondensed Matter Physics0104 chemical sciencesCrystallographylcsh:QD1-999hydrogen-bonding patternsActa Crystallographica Section E Crystallographic Communications
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Crystal structure of bis{μ2-3-(pyridin-2-yl)-5-[(1,2,4-triazol-1-yl)methyl]-1,2,4-triazolato}bis[aquanitratocopper(II)] dihydrate

2016

The title complex is a centrosymmetric dimer with a copper–copper distance of 4.0408 (3) Å. The Cu ions in the dimer are bridged by two triazole rings and oxygen donor ligands from water mol­ecules and nitrate anions in a distorted octa­hedral coordination geometry.

crystal structureDimerTriazoledinuclear copper complexchemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesResearch CommunicationsCrystalchemistry.chemical_compound124-triazoleGeneral Materials ScienceCoordination geometryCrystallography010405 organic chemistryHydrogen bond124-TriazoleGeneral ChemistryCondensed Matter PhysicsCopper0104 chemical sciencesCrystallographychemistryQD901-999hydrogen bondsActa Crystallographica Section E: Crystallographic Communications
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Crystal structure and Hirshfeld surface analysis of 2-[(1,3-benzoxazol-2-yl)sulfanyl]-N-(2-methoxyphenyl)acetamide

2019

Akkurt, Mehmet/0000-0003-2421-0929; Saylam, Merve/0000-0002-7602-4565

crystal structureHydrogen bondGeneral ChemistryCrystal structureDihedral angleCondensed Matter::Mesoscopic Systems and Quantum Hall Effecthydrogen bonding010402 general chemistry010403 inorganic & nuclear chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciences13-benzoxazole ring system0104 chemical scienceslcsh:ChemistryCrystaldimerschemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryHirshfeld surface analysisGeneral Materials ScienceBenzeneAcetamideActa Crystallographica Section E Crystallographic Communications
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Crystal structure of (E)-pent-2-enoic acid

2015

The molecule of the title compound, C5H8O2, a low-melting α,β-unsaturated carboxylic acid, is essentially planar [maximum displacement = 0.0239 (13) Å]. In the crystal, molecules are linked into centrosymmetric dimersviapairs of O—H...O hydrogen bonds.

crystal structurehydrogen bondunsaturated carb­oxy­lic acidHydrogen bondDimerGeneral ChemistryCrystal structureCondensed Matter Physicscomputer.software_genredimerData ReportsCrystallcsh:ChemistryCrystallographychemistry.chemical_compoundPlanarchemistrylcsh:QD1-999General Materials ScienceData miningMaximum displacementcomputerunsaturated carboxylic acidActa Crystallographica Section E: Crystallographic Communications
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1,1-Diphenyl-4-(thiophen-2-yl)but-3-yn-1-ol

2018

The asymmetric unit of the title homopropargyl alcohol, C20H16OS, contains two independent molecules comprising a hydroxy group, a 3-(2-thiophenyl)- propargylic moiety and two aromatic rings linked to a central carbon atom. The two unique molecules are linked into a dimer by an O—HO hydrogen bond. In one molecule, the thiophene ring is disordered over two orientations rotated by 180 with a refined occupancy ratio of 0.575 (4):0.425 (4). The crystal structure is stabilized by O—H and C—H hydrogen-bond interactions. The crystal studied was a two-component non-merohedral twin, the refined ratio of the twin components being 0.575 (4):0.425 (4). UCR::Vicerrectoría de Docencia::Ciencias Básicas::…

crystal structurepropargylationHomopropargyl alcoholsDimer13-dilithiopropyneCrystal structurealkynes010402 general chemistryRing (chemistry)01 natural sciencesCrystalchemistry.chemical_compoundlcsh:QD901-999MoleculeMoiety010405 organic chemistryHydrogen bondCrystal structurePropargylationAromaticity0104 chemical sciences13-dili­thio­propyneCrystallographychemistryAlkynes540 Químicahomopropargyl alcoholslcsh:Crystallography
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Synthesis, structural, and thermal characterization of a new binuclear copper(II) chelate complex bearing an amine-hardener for epoxy resins

2016

A new di(μ-carbonato)bis[aqua(diethylenetriamine)copper(II)] hexahydrate complex, [{Cu(NH(C2H4NH2)2)(H2O)(μ-CO3)}2]⋅6H2O (1), was synthesized by direct interaction of malachite with diethylenetriamine (dien). The crystals of 1 were characterized by X-ray powder diffraction and IR spectra, as well as structurally characterized. Compound 1 consists of [{Cu(dien)(H2O)(μ-CO3)}2] discrete units whose CO32– anions play the role of bridging ligands combining two Cu(II) chelate cores into a centrosymmetric dimer. The elongated octahedral environment of Cu2+ consists of three nitrogens of dien and an oxygen from CO32– at the base of the bipyramid; the two apical positions of such polyhedron are occu…

differential thermal analysisfire retardant-hardeners of epoxy resinsCopper(II) chelate complexessynthesisHydrogen bondDimerThermal decompositionInorganic chemistrychemistry.chemical_element010402 general chemistry010403 inorganic & nuclear chemistryX-ray crystal structure01 natural sciencesCopper0104 chemical scienceschemistry.chemical_compoundCrystallographyBipyramidchemistryOctahedronIR spectroscopyDifferential thermal analysisDiethylenetriamineMaterials ChemistryPhysical and Theoretical ChemistryJournal of Coordination Chemistry
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Quinoidal oligothiophenes: towards biradical ground-state species.

2009

A family of quinoidal oligothiophenes, from the dimer to the hexamer, with fused bis(butoxymethyl)cyclopentane groups has been extensively investigated by means of electronic and vibrational spectroscopy, electrochemical measurements, and density functional calculations. The latter predict that the electronic ground state always corresponds to a singlet state and that, for the longest oligomers, this state has biradical character that increases with increasing oligomer length. The shortest oligomers display closed-shell quinoidal structures. Calculations also predict the existence of very low energy excited triplet states that can be populated at room temperature. Aromatization of the conju…

education.field_of_studyDimerOrganic ChemistryPopulationInfrared spectroscopyGeneral ChemistryElectronic structurePhotochemistryCatalysischemistry.chemical_compoundchemistryExcited stateSinglet statePhysics::Chemical PhysicsTriplet stateGround stateeducationChemistry (Weinheim an der Bergstrasse, Germany)
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Dosaggio del D-dimero "alta sensibilità" (D-D HS): valutazione del test e applicazioni nella pratica laboratoristica (risultati preliminari)

2009

emostasiD-DimeroSettore MED/42 - Igiene Generale E Applicata
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Allocation of Ambipolar Charges on an Organic Diradical with a Vinylene-Phenylenediyne Bridge.

2021

Two redox and magnetically active perchlorotriphenylmethyl (• PTM) radical units have been connected as end-capping groups to a bis(phenylene)diyne chain through vinylene linkers. Negative and positive charged species have been generated, and the influence of the bridge on their stabilization is discussed. Partial reduction of the electron-withdrawing • PTM radicals results in a class-II mixed-valence system with the negative charge located on the terminal PTM units, proving the efficiency of the conjugated chain for the electron transport between the two terminal sites. Counterintuitively, the oxidation process does not occur along the electron-rich bridge but on the vinylene units. The • …

endocrine system010405 organic chemistryRadical anion010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesPolitical scienceOxidationGeneral Materials ScienceStilbene analoguePhysical and Theoretical ChemistryPTM radicalMixed-valence speciesHumanitiesDimerizationOligoyneThe journal of physical chemistry letters
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