Search results for "hydrogen"

showing 10 items of 4254 documents

tert-ButylN-(4-methyl-2-pyridyl)carbamate

2008

The crystal structure of the title compound, C11H16N2O2, contains two crystallographically independent molecules forming dimers by pairs of intermolecular N—H...N hydrogen bonds. The two molecules are related by a pseudo-twofold axis. The dihedral angle between the pyridine ring and the carbamate plane differs in the two molecules [12.1 (3) and 3.5 (3)°].

Tert butylCarbamateHydrogen bondChemistrymedicine.medical_treatmentGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsBioinformaticsRing (chemistry)Organic PapersMedicinal chemistrylcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999PyridinemedicineGeneral Materials ScienceActa Crystallographica Section E Structure Reports Online
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2,4-Di-tert-butyl-6-({[2-(di-methyl-amino)-eth-yl](2-hy-droxy-benz-yl)amino}-meth-yl)phenol.

2014

The title compound, C26H40N2O2, has both its N atoms in trigonal-pyramidal geometries. The molecular structure is stabilized by O—H...N and C—H...O hydrogen bonds. In the crystal, C—H...π interactions lead to the formation of a supramolecular helical chain along theb-axis direction.

Tert butylQuantitative Biology::BiomoleculesCrystallographyChemistryHydrogen bondSupramolecular chemistryGeneral ChemistryMeth-Condensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic PapersHelical chainchemistry.chemical_compoundQD901-999PhenolGeneral Materials ScienceActa crystallographica. Section E, Structure reports online
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Bis(tert-butylammonium) oxalate

2006

The component species in the title compound, 2C4H12N2+·C2O42−, inter­act by way of N—H⋯O hydrogen bonds, resulting in a layered network. N and two C atoms of the cation possess site symmetry m and the C atom of the anion has site symmetry 2.

Tert butylchemistry.chemical_compoundchemistryHydrogen bondAtomGeneral Materials ScienceGeneral ChemistryAmmonium oxalateCondensed Matter PhysicsMedicinal chemistryIonActa Crystallographica Section E Structure Reports Online
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CCDC 125321: Experimental Crystal Structure Determination

1996

Related Article: J.Faus, F.Lloret, M.Julve, J.M.Clemente-Juan, M.C.Munoz, X.Solans, M.Font-Bardia|1996|Angew.Chem.,Int.Ed.|35|1485|doi:10.1002/anie.199614851

Tetra-potassium hexa-aqua-nickel(ii) decakis(hydrogen violurato)-bis(dihydrogen violurato)-hexahedro-octa-nickel(ii) icosahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Dimeric Capsules Formed by Tetra-CMPO Derivatives of (Thia)Calix[4]arenes

2010

Thiacalix[4]arene 2, calix[4]arene 3 a and its tetraether fixed in the cone conformation 3 b form homo- and heterodimeric capsules in apolar solvents, which are held together by a seam of NH⋅⋅⋅O=P hydrogen bonds between carbamoylmethyl phospine oxide functions attached to their wide rim. Their internal volume of ∼370 A3 requires the inclusion of a suitable guest. Although neutral molecules such as adamantane (derivatives) or tetraethylammonium cations form kinetically stable complexes (1H- and 31P-time scale), the included solvent is rapidly exchanged. The internal mobility of the included tetraethylammonium cation is distinctly higher (ΔG=42.5 and 49.7 kJ mol−1 for 3 a and 3 b) than that f…

TetraethylammoniumbiologyHydrogen bondAdamantaneOrganic ChemistryCationic polymerizationGeneral Chemistrybiology.organism_classificationBiochemistrySolventchemistry.chemical_compoundchemistryCalixarenePolymer chemistryMoleculeTetraChemistry - An Asian Journal
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Synthesis, characterization, crystal structures and magnetic exchange in dinuclear copper complexes with 3-amino-1-propanol as terminal and bridging …

1990

Abstract The synthesis, X-ray structures and spectroscopic and magnetic properties are described for two groups of dinuclear Cu(II) compounds with the ligand 3-amino-1-propanol (Hap). The formulae of the compounds are for group A: [Cu(ap)(anion)]2, in which ap is the dehydronated Hap and the anions are formate, nitrate, chloride and bromide and for group B: [Cu(ap)(Hap)]2(anion)2, with anion = iodide, bromide, chloride, nitrate and tetrafluoroborate. The structure of group A compounds consists of dinuclear units with the co-planar centrosymmetric chromophore ANCuOO′CuNA, in which the A ligands (anions) bridge to neighbouring units as axial ligands, thereby forming infinite chains. Dimer Cu……

TetrafluoroborateCoordination sphereChemistryHydrogen bondStereochemistryLigandDimerBridging ligandCrystal structureSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundCrystallographyMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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The role of the dual nature of ionic liquids in the reversed-phase liquid chromatographic separation of basic drugs.

2010

The cationic nature of basic drugs gives rise to broad asymmetrical chromatographic peaks with conventional C18 columns and hydro-organic mixtures, due to the ionic interaction of the positively charged solutes with the free silanol groups on the alkyl-bonded reversed-phase packing. Ionic liquids (ILs) have recently attracted some attention to reduce this undesirable silanol activity. ILs are dual modifiers (with a cationic and anionic character), which means that both cation and anion can be adsorbed on the stationary phase, giving rise to interesting interactions with the anionic free silanols and the cationic basic drugs. A comparative study of the performance of four imidazolium-based I…

TetrafluoroborateIonic bondingIonic LiquidsBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhase (matter)BoratesEthylaminesTriethylamineChromatography Reverse-PhaseChromatographyOrganic ChemistryCationic polymerizationImidazolesSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationSilanesSilanolchemistryModels ChemicalPharmaceutical PreparationsIonic liquidLinear ModelsJournal of chromatography. A
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Synthesis, crystal structure, spectroscopic characterisation and magnetic properties of [Cu2(BIBM)2(C2O4)2]·4H2O (BIBM=bis(2-imidazolyl)bis(methoxyca…

2001

Abstract The structure and spectroscopic and magnetic properties of bis(μ-1,2,3-oxalato)bis[bis(2-imidazolyl)bis(methoxycarbonyl)methylmethane]dicopper(II) tetrahydrate are described. The compound is built of centrosymmetric neutral dimeric [Cu2(BIBM)2(C2O4)2] entities linked through hydrogen bonds involving water molecules and oxalate groups. In the dimeric unit the two centrosymmetrically related copper — which are involved in CuN2O2O2′ chromophores lying in an elongated octahedral environment — are bridged through the oxalate group which acts in a bidentate–monodentate (μ-1,2,3) fashion. Both electronic and EPR spectra are indicative of an essentially dx2−y2 ground state for the copper(I…

TetrahydrateChemistryHydrogen bondStereochemistryCrystal structureMagnetic susceptibilityOxalatelaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronlawMaterials ChemistryMoleculePhysical and Theoretical ChemistryElectron paramagnetic resonanceInorganica Chimica Acta
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Tris(1,10-phenanthroline)zinc(II) dichromate tetrahydrate

2002

The title compound, [Zn(C12H8N2)3][Cr2O7]·4H2O, was obtained by mixing 1,10-phenanthroline (phen), potassium chromate and zinc sulfate solutions. The asymmetric unit is composed of a [Zn(phen)3]2+ cation, a Cr2O72− anion and four water mol­ecules. The ZnII ion is in a distorted octahedral environment, coordinated by six N atoms from three phen mol­ecules. The cations are connected to anions by weak C—H⋯O hydrogen bonds, with shortest H⋯O distances of ca 2.27–2.33 A. The Cr2O72− anion is in a staggered conformation. Two of the four crystallographically independent water mol­ecules are ordered, and two others are disordered, each over two sites.

TetrahydrateHydrogen bondPhenanthrolinechemistry.chemical_elementGeneral ChemistryZincStaggered conformationCondensed Matter PhysicsIonchemistry.chemical_compoundCrystallographychemistryOctahedronGeneral Materials SciencePotassium chromateActa Crystallographica Section E Structure Reports Online
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The role of cation⋯π interactions in capsule formation: co-crystals of resorcinarenes and alkyl ammonium salts

2008

An unprecented dimeric capsular assembly of a tetramethylated C-hexyl resorcinarene and an expected one from unsubstituted C-butyl resorcinarene with tetramethylammonium cation are described. Surprisingly tetramethylated C-hexyl resorcinarene, with no apparent possibility for intra-capsular hydrogen bonds, forms a capsule which is held together solely by the cation⋯π interactions and the complementary geometry of the spherical guest cation and the concave resorcinarene host. The C-butyl resorcinarene capsule, as in the case of dimeric resorcinarene capsules reported earlier, is mediated viasolvent molecules and intra-capsular hydrogen bonds. We also report here two co-crystals of C-methyl r…

Tetramethylammoniumchemistry.chemical_classificationStereochemistryHydrogen bondHalideGeneral ChemistryResorcinareneCondensed Matter PhysicsCrystalchemistry.chemical_compoundchemistryPolymer chemistryMoleculeGeneral Materials ScienceAmmoniumAlkylCrystEngComm
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