Search results for "X-ray structure"

showing 10 items of 32 documents

From self-inclusion and host-guest complexes to channel structures

2012

Various supramolecular interactions are applied as driving forces in self-assembly and molecular recognition processes. Single crystal X-ray diffraction method is especially important for solid-state studies of non-covalent interactions as it reveals their influence on the molecular and supramolecular structures. This paper discusses structures of two completely different types of compounds in which a variety of intermolecular interactions are involved. It will be shown that strong and weak intermolecular hydrogen bonds in N-alkylammonium resorcinarene salts, depending on the type of anion, inclusion of resorcinarene upper rim pendant group or solvent molecules into the cavity, strongly aff…

010405 organic chemistryChemistryStereochemistryX-ray structure; supramolecular chemistry; hydrogen bonding; hydrophobic interaction; resorcinarene; palladium complexSupramolecular chemistryGeneral ChemistryInclusion (mineral)010402 general chemistryta11601 natural sciencesHost (network)0104 chemical sciencesCommunication channel
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Equipping metallo-supramolecular macrocycles with functional groups: Assemblies of pyridine-substituted urea ligands

2012

A series of di-(m-pyridyl)-urea ligands were prepared and characterized with respect to their conformations by NOESY experiments and crystallography. Methyl substitution in different positions of the pyridine rings provides control over the position of the pyridine N atoms relative to the urea carbonyl group. The ligands were used to self-assemble metallo-supramolecular M(2)L(2) and M(3)L(3) macrocycles which are generated in a finely balanced equilibrium in DMSO and DMF according to DOSY NMR experiments and ESI FTICR mass spectrometry. Again, crystallography was used to characterize the assemblies. Methyl substitution in positions next to the pyridine nitrogen prevents coordination, while …

010405 organic chemistryHydrogen bondChemistryStereochemistrySupramolecular chemistryurea ligands; metallo-supramolecular macrocycles; X-ray structure; hydrogen-bonding010402 general chemistryMass spectrometry01 natural sciencesFourier transform ion cyclotron resonance0104 chemical sciencesInorganic ChemistrySubstituted ureaCrystallographychemistry.chemical_compoundPyridineUreaTwo-dimensional nuclear magnetic resonance spectroscopyta116Dalton Transactions
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Preparation and molecular structures of N′-(2-heteroarylmethylidene)-3-(3-pyridyl)acrylohydrazides

2018

Abstract The crystal and molecular structures of N′-(2-furylmethylidene)-3-(3-pyridyl)acrylohydrazide and N′-(2-thienylmethylidene)-3-(3-pyridyl)acrylohydrazide are reported, and the influence of the type of the heteroatom on the aromaticity of the aromatic rings is discussed. Both molecules are nearly planar. The geometry of the acrylohydrazide arrangement is comparable to that of homologous compounds. Density functional theory (DFT) calculations were performed in order to analyze the changes in the geometry of the studied compounds in the crystalline state and for the isolated molecule. The most significant changes were observed in the values of the N–N and C–N bond lengths. The harmonic …

0301 basic medicinecrystal structure010405 organic chemistryChemistryacroylhydrazidesaromaticityGeneral ChemistryX-ray structure determination01 natural sciences0104 chemical sciences03 medical and health sciences030104 developmental biologyPolymer chemistryquantum chemical calculationsdensity functional theoryheteroaryl substituentsZeitschrift für Naturforschung B
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Binding Modes of Nonspherical Anions to N-Alkylammonium Resorcinarenes in the Solid State

2012

A series of hydrogen bond stabilized N-alkylammonium resorcinarene salts with nitrate, triflate, and picrate as the counteranions were synthesized and characterized with 1H NMR and electrospray ionization (ESI) mass spectrometry. Together with electrostatic interactions, the binding of the anions with several hydrogen bond donor sites proceeds through a complex array of intra- and intermolecular hydrogen bonds, evidenced by single crystal X-ray diffraction analysis. These N-alkyl ammonium resorcinarenes bind the larger nonspherical anions into deformed cavitand-like structures and enforce a transformation of the resorcinarene conformation from almost symmetrical to extremely distorted.

ChemistryHydrogen bondPicrateElectrospray ionizationIntermolecular forceInorganic chemistryGeneral ChemistryResorcinareneCondensed Matter PhysicsMass spectrometrychemistry.chemical_compoundCrystallographyProton NMRGeneral Materials ScienceTrifluoromethanesulfonateta116resorcinarenes; non-spherical anions; hydrogen bonding; X-ray structureCRYSTAL CROWTH & DESIGN
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Hydrogen bond-stabilised N-alkylammonium resorcinarene halide cavitands

2010

A family of hydrogen bond-stabilised N-alkylammonium resorcinarene chloride and bromide cavitands were synthesised and characterised with 1H NMR and ESI mass spectrometry. The seven compounds exhibit interestingly either self-inclusion or guest complexation in the solid state evidenced by single crystal X-ray diffraction. The four dimers show self-inclusion of the upper rim propyl chains and consist of two hydrogen-bonded resorcinarene tetracations and six halide anions, while the remaining two halide anions are located in between the dimers linking them via hydrogen bonding. Small solvent molecules such as dichloromethane, methanol, n-butanol or chloroform are complexed into the resorcinar…

ChloroformHydrogen bondHalideGeneral ChemistryResorcinarenePhotochemistrySolventchemistry.chemical_compoundchemistryBromidePolymer chemistryProton NMRMoleculeresorcinarenes; tetrabenzoxazines; ammonium halides; hydrogen bonding; X-ray structure
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Interaction of half-sandwich alkylmolybdenum(III) complexes with B(C6F5)3. The X-ray structure of [CpMo(η4-C4H6)(μ-Cl)(μ-CH2)(O)MoCp][CH3B(C6F5)3]

2001

Abstract The reactions of the half-sandwich molybdenum(III) complexes CpMo(η 4 -C 4 H 4 R 2 )(CH 3 ) 2 , where Cpη 5 -C 5 H 5 and RH or CH 3 , with equimolar amounts of B(C 6 F 5 ) 3 have been investigated in toluene. EPR monitoring shows the formation of an addition product which does not readily react with Lewis bases such as ethylene, pyridine, or PMe 3 . The analysis of the EPR properties and the X-ray structure of a decomposition product obtained from dichloromethane, [CpMo(η 4 -C 4 H 6 )(μ-Cl)(μ-CH 2 )(O)MoCp][CH 3 B(C 6 F 5 ) 3 ], indicate that the borane attack has occurred at the methyl position.

EthyleneStereochemistrychemistry.chemical_elementBorane010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundlawPyridineMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryLewis acids and basesPhysical and Theoretical ChemistryElectron paramagnetic resonanceDichloromethaneMolybdenumEPR properties010405 organic chemistryOrganic ChemistryTolueneButadiene ligand0104 chemical sciences3. Good healthchemistryHalf-sandwichMolybdenumX-ray structure
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N-(4-Acetyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N-methyl-2-(2-methyl-4-oxo-3,4-dihydroquinazolin-3-yl)benzamide

2013

In the title compound, C29H25N5O3, the dihedral angle between the benzene ring and the pendant quinazoline ring system (r.m.s. deviation = 0.036Å) is 87.60 (17)°. The equivalent angle between the pyrazole ring and the phenyl group is 70.0 (2)°. The dihedral angle between the benzene and pyrazole rings is 30.7 (2)° and overall, the molecular conformation approximates to a Z shape. A short intramolecular C—H...O contact occurs. In the crystal, the molecules are linked by Cπ—H...O-type hydrogen bonds and aromatic π–π stacking interactions [centroid–centroid distance = 3.860 (3) Å], generating a three-…

Hydrogen bondQuinazolinylbenzamide derivative X-ray structureStackingGeneral ChemistryDihedral anglePyrazoleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic PapersMedicinal chemistrySettore CHIM/08 - Chimica Farmaceuticalcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999QuinazolinePhenyl groupGeneral Materials ScienceBenzeneActa Crystallographica Section E
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Resolution of β-aminophosphines with chiral cyclopalladated complexes

2005

Abstract Resolution of the racemic chiral β-aminophosphines Ph 2 PCH 2 CH(Ph)NH(Ar) ( L 1 for Ar = C 6 H 5 and L 2 for Ar = 2,6-C 6 H 3 i Pr 2 ) has been investigated by use of different cyclopalladated complexes as chiral agents. The resulting complexes afford diastereomeric adducts in a 1:1 ratio. After successive crystallizations from ethanol, a d.e. of 98% was achieved for one aminophosphine palladium complex, while no significant d.e. was obtained after crystallizations from chlorinated solvents. The X-ray structure analysis has pointed out intermolecular hydrogen interactions N–H⋯Cl between the P,N ligand and the chloride ion, which are responsible for the formation and stabilization …

HydrogenAminophosphinesStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryChlorideMedicinal chemistryAdductInorganic ChemistryMaterials Chemistrymedicine[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryLigandOrganic ChemistryIntermolecular forceDiastereomerAbsolute configuration0104 chemical scienceschemistryPN ligandsRacemic resolutionChiral palladium complexesX-ray structuresPalladiummedicine.drugJournal of Organometallic Chemistry
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N2,N2.N6,N6-Tetrakis(perfluorobenzoyl)-2,6-diaminopyridine

2011

The title compound, C³³H³F²⁰N³O⁴, is a highly fluorinated organic imide that was isolated as an unexpected product from the reaction of 2,6-diaminopyridine with 2,3,4,5,6-pentafluorobenzoyl chloride in a 1:2 molar ratio. The molecule is located on a twofold axis and one of its symmetry-independent 2,3,4,5,6-pentafluorobenzoyl groups is disordered over two sets of sites, the occupancy of the major component being 0.773 (3). In the major component, the dihedral angle between the perfluorophenyl groups is 63.64 (10)°, and these groups form dihedral angles of 67.14 (7) and 21.1 (2)° with the pyridine core. Short intermolecular C-HO and C-H...N contacts are found in the crystal structure. peerRe…

KiderakenneCrystal structureRöntgenrakenneX-ray structure
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Lanthanide molecular oxohydroxides: Synthesis and characterisation of [Y4(μ4-O)(μ-OEt)2(μ,η2-AAA)2(η2-AAA)3]2(μ3-OH)4(μ3-OEt)2 (HAAA = allylacetatoac…

2007

International audience; The reaction between Y5O(OPri)13 and allylacetatoacetate or 2-(methacryloyloxy)ethyl acetatoacetate in 1:5 stoichiometry afforded octanuclear oxohydroxo species. Structural characterization was achieved for the allylacetatoacetate derivative homo and copolymerisation reactions with styrene were evaluated for doping of polystyrene. Hydoxo species, Y4(OH)2(AAA)10, where also obtained by reacting Y[N(SiMe3)]3 and HAAA.

LanthanideInorganic chemistrychemistry.chemical_element02 engineering and technologyAlkoxides010402 general chemistry01 natural sciences"Polymerizable ligands"StyreneInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryYttriumPhysical and Theoretical ChemistryPolymerizable ligands"Alkoxides"Doping"X-ray structure"Yttrium[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnology[SDE.ES]Environmental Sciences/Environmental and Society0104 chemical scienceschemistryPolystyreneX-ray structure0210 nano-technology"Yttrium"Derivative (chemistry)Stoichiometry
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