Search results for "Substitution reactions"

showing 4 items of 4 documents

trans-4-Bromo-ONN-azoxybenzene at 100 K.

2004

The crystal structure of the alpha isomer of trans-4-bromoazoxybenzene [systematic name: trans-1-(bromophenyl)-2-phenyldiazene 2-oxide], C(12)H(9)BrN(2)O, has been determined by X-ray diffraction. The geometries of the two molecules in the asymmetric unit are slightly different and are within approximately 0.02 A for bond lengths, approximately 2 degrees for angles and approximately 3 degrees for torsion angles. The azoxy bridges in both molecules have the typical geometry observed for trans-azoxybenzenes. The crystal network contains two types of planar molecules arranged in columns. The torsion angles along the Ar-N bonds are only 7 (2) degrees, on either side of the azoxy group.

DiffractionAzoxyCrystal structureIsomersTorsion (mechanics)X ray diffraction analysisGeneral MedicineCrystal structureMolecular dynamicsGeneral Biochemistry Genetics and Molecular BiologyBond lengthCrystalchemistry.chemical_compoundCrystallographyTorsional stressMolecular geometrychemistrySubstitution reactionsOxidationMoleculeActa crystallographica. Section C, Crystal structure communications
researchProduct

H−ZSM-5 Modified Zeolite:  Quantum Chemical Models of Acidic Sites

2007

A ZSM-5 fragment, containing 52 tetrahedral moieties, each of them formed by one silicon or one aluminum atom surrounded by four oxygen atoms, was employed to model (52T systems) by quantum chemical calculations (i) the influence of the positions of the acidic sites on the energetics of 22 aluminum monosubstituted and bisubstituted 52T acidic zeolite (H-ZSM-5) systems and (ii) the local adsorption properties and acidic strength of the corresponding -OH sites. The energetics and the structural properties of simpler acid H-ZSM-5 systems containing only five Tetrahedral moieties (5T systems) were also modeled for comparison. B3LYP/6-31G(d,p) partial geometry optimization routines were performe…

ONIOMSiliconChemistryAdsorption Computational methods Molecular modeling Molecular structure Quantum chemistry Substitution reactionschemistry.chemical_elementSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyAdsorptionAluminiumComputational chemistryAtomTetrahedronPhysical chemistryPhysical and Theoretical ChemistryZSM-5ZeoliteThe Journal of Physical Chemistry C
researchProduct

Synthesis, crystal and molecular-electronic structure, and kinetic investigation of two new sterically hindered isomeric forms of the dimethyl[methyl…

2017

Two new structural isomers – 2,4-dimethyl-5-[methyl(phenylsulfonyl)amino]benzenesulfonyl chloride (1) and 2,4-dimethyl-3-[methyl(phenylsulfonyl)amino]benzenesulfonyl chloride (2) were synthesized by interaction of N-(2,4-dimethylphenyl)-N-methyl-benzenesulfonamide or N-(2,6-dimethylphenyl)-N-methylbenzenesulfonamide with chlorosulfonic acid. Both compounds have been structurally characterized by X-ray single crystal diffraction at 100 K. The crystals of 1 are triclinic: space group View the MathML source, a = 8.1542(2), b = 11.0728(3), c = 11.2680(3) Å, α = 116.557(3), β = 95.155(2), γ = 108.258(2)°, V = 831.97(4) Å3, Z = 2, R = 0.0251 for 2429 reflections; the crystals of 2 are monoclinic:…

Steric effectsSubstitution reaction010405 organic chemistryStereochemistryHydrogen bondOrganic ChemistryTriclinic crystal system010402 general chemistry01 natural sciencesKinetics of substitution reactions in aqueous solution0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographychemistry.chemical_compoundQuantum-chemical analysischemistryX-ray crystal structure determinationIntramolecular forceBenzenesulfonyl chlorideStructural isomerMoleculeOrtho-effectSterically hindered derivatives of aromatic sulfonic acidsSpectroscopyJournal of Molecular Structure
researchProduct

A new mechanism for internal nucleophilic substitution reactions

2018

A new mechanism for the classic internal nucleophilic substitution reactions SNi by means of computational studies in the gas-phase, DCM and acetonitrile is reported. Despite the importance of the SNi mechanism, since the mid-1990s this mechanism has remained unexplored. This study focused mainly on the comparison between the mechanisms postulated to date for the SNi reactions and a new mechanism suggested by us that fits better the experimental observations. This comparative study has been applied to the conversion of ethyl, neopentyl, isopropyl and tert-butyl chlorosulfites into the corresponding alkyl chlorides. This new mechanism occurs through two transition structures. For primary and…

Substitution reaction010405 organic chemistryChemistryOrganic ChemistryInternal substitution reaction010402 general chemistryDFT01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesGovernment (linguistics)Substitution reactionsNucleophilic substitutionMechanismPhysical and Theoretical ChemistryMechanism (sociology)Organic & Biomolecular Chemistry
researchProduct