Search results for " Geometry."

showing 10 items of 2189 documents

Mössbauer study of the solid state configuration of triorganotin derivatives with intramolecular coordination

1980

Triorganotin bromides with intramolecular nitrogen-to-tin coordination (I-VIII, Fig. 1) have been structurally investigated by Mossbauer and infrared spectroscopy. Mossbauer-Zeeman spectra have been measured for I and VIII in order to obtain the sign of the nuclear quadrupole splitting ΔE and the value of the asymmetry parameter η. Point-charge model values of ΔE and η have been calculated for environments of tin atoms in I-VIII which are plausible in view of the results of previous investigations. From trends of experimental ΔE in the series, and from the agreement between experimental and calculated Mossbauer parameters it is concluded that the compounds I-VIII all have trigonal bipyramid…

Stereochemistrymedia_common.quotation_subjectInfrared spectroscopychemistry.chemical_elementQuadrupole splittingAsymmetrySpectral lineInorganic ChemistryTrigonal bipyramidal molecular geometryCrystallographychemistryIntramolecular forceMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinmedia_commonInorganica Chimica Acta
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Weak Interactions Modulating the Dimensionality in Supramolecular Architectures in Three New Nickel(II)-Hydrazone Complexes, Magnetostructural Correl…

2011

Three different ONO donor acetyl hydrazone Schiff bases have been synthesized from the condensation of acetic hydrazide with three different carbonyl compounds: salicylaldehyde (HL(1)), 2-hydroxyacetophenone (HL(2)), and 2, 3-dihydroxybenzaldehyde (HL(3)). These tridentate ligands are reacted with Ni(OOCCF(3))(2)·xH(2)O to yield three new Ni(II) complexes having distorted octahedral geometry at each Ni center: [Ni(L(1))(OOCCF(3))(CH(3)OH)](2) (1), [Ni(L(2))(OOCCF(3))(H(2)O)](2) (2), and [Ni(L(3))(L(3)H)](OOCCF(3))(H(2)O)(1.65)(CH(3)OH)(0.35) (3). The ligands and the complexes have been characterized by elemental analysis and IR and UV-vis spectroscopy, and the structures of the complexes ha…

Steric effectsModels MolecularStereochemistryMacromolecular SubstancesDimerSupramolecular chemistryHydrazoneAlkenes[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryCrystallography X-RayLigands01 natural sciencesCatalysisPhase TransitionInorganic Chemistrychemistry.chemical_compoundMagneticsNickelOctahedral molecular geometryMagnetic propertiesOrganometallic Compounds[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesPhysical and Theoretical Chemistrychemistry.chemical_classificationMolecular StructureCatalysts010405 organic chemistryChemistryHydrogen bondLigandHydrazonesHydrocarbons0104 chemical sciencesCrystallographySalicylaldehydeOligomersEpoxy Compounds
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DNA interaction of new copper(II) complexes with sulfonamides as ligands

2007

New copper(II) complexes with sulfonamide ligands have been prepared and characterized. Sulfonamide ligands were prepared through a reaction between 8-aminoquinoline and either 2-mesitylene (Hqmesa), 4-tert-butylbenzene (Hqtbsa), or alpha-toluene (Halphaqtsa) sulfonyl chlorides. The structural analysis carried out for complex [Cu(alphaqtsa)(2)] indicated that the local environment of the Cu(II) cation is between a square planar and a tetrahedral geometry, with stacking of the benzene rings of the sulfonyl ligands between neighbor molecules. Powder EPR spectra at room temperature gave rhombic spectra for the [Cu(alphaqtsa)(2)] and [Cu(qmesa)(2)] complexes and an axial spectrum for the [Cu(qt…

Steric effectsMolecular Conformationchemistry.chemical_elementAscorbic AcidCrystallography X-RayPhotochemistryBiochemistryMedicinal chemistrylaw.inventionInorganic ChemistrylawOrganometallic CompoundsMoleculeSinglet stateElectron paramagnetic resonancechemistry.chemical_classificationSulfonylSulfonamidesMolecular StructureTetrahedral molecular geometryDNACopperIntercalating AgentsSulfonamidechemistryReactive Oxygen SpeciesCopperPlasmidsJournal of Inorganic Biochemistry
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Dispersion Forces and Counterintuitive Steric Effects in Main Group Molecules: Heavier Group 14 (Si-Pb) Dichalcogenolate Carbene Analogues with Sub-9…

2013

The synthesis and spectroscopic and structural characterization of an extensive series of acyclic, monomeric tetrylene dichalcogenolates of formula M(ChAr)2 (M = Si, Ge, Sn, Pb; Ch = O, S, or Se; Ar = bulky m-terphenyl ligand, including two new acyclic silylenes) are described. They were found to possess several unusual features-the most notable of which is their strong tendency to display acute interligand, Ch-M-Ch, bond angles that are often well below 90°. Furthermore, and contrary to normal steric expectations, the interligand angles were found to become narrower as the size of the ligand was increased. Experimental and structural data in conjunction with high-level DFT calculations, in…

Steric effectsMolecular StructureChemistryLigandStereochemistryGeneral ChemistryBiochemistryLondon dispersion forceCatalysischemistry.chemical_compoundCrystallographyColloid and Surface ChemistryMonomerMolecular geometryOrganometallic CompoundsChalcogensQuantum TheoryMoleculeDispersion (chemistry)MethaneCarbeneta116Journal of the American Chemical Society
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EPR spectroscopic characterization of persistent germyl-substituted Pb(III)- and Sn(III)-radicals.

2010

In this report we present the synthesis and the detailed electron paramagnetic resonance (EPR) spectroscopic characterization of novel trivalent lead- and tin-based radicals comprising sterically demanding germyl substituents. The investigated radicals are derived from the recently reported trihypersilyl-substituted tetryl radicals *PbHyp3 and *SnHyp3. The tetryl radicals *Pb(Ge(SiMe3)3)3 (8), *Pb(Ge(SiMe3)3)2Si(SiMe3)3 (9), *PbGe(SiMe3)3(Si(SiMe3)3)2 (10), and *Sn(Ge(SiMe3)3)3 (11) show substitution patterns derived from stepwise (9, 10) or complete (8, 11) substitution of hypersilyl groups (Hyp = Si(SiMe3)3) in *PbHyp3 and *SnHyp3 by homologous hypergermyl groups (Hge = Ge(SiMe3)3). They …

Steric effectsNucleophilic additionChemistryStereochemistryRadicalSubstituentlaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundMolecular geometrylawMolecular orbitalElectron paramagnetic resonanceHyperfine structureDalton transactions (Cambridge, England : 2003)
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Synthesis, spectroscopic characterization and in vitro antimicrobial activity of diorganotin(IV) dichloride adducts with [1,2,4]triazolo-[1,5-a]pyrim…

2006

Abstract The heterocyclic ligands [1,2,4]triazolo-[1,5-a]pyrimidine (tp) and 5,7-dimethyl-[1,2,4]triazolo-[1,5-a]pyrimidine (dmtp), react with diorganotin dichlorides giving the addition compounds Me2SnCl2(tp)2, Et2SnCl2(tp)2, Me2SnCl2(dmtp)2, Et2SnCl2(dmtp)2, Bu2SnCl2(dmtp), Ph2SnCl2(dmtp). The organotin:ligand stoichiometry goes from 1:2 to 1:1 by increasing the steric hindrance of the organic groups bound to tin. The compounds have been characterized by means of infrared, 119Sn Mossbauer and 1H AND 13C NMR spectroscopy. The ligands presumably coordinate to tin classically through the nitrogen atom at the position 3. The 1:1 complexes adopt trigonal bipyramidal structures, with the organi…

Steric effectsPyrimidineLigandStereochemistryOrganic ChemistryDFT calculationchemistry.chemical_elementAntimicrobial activityBiochemistryMedicinal chemistryTriazolopyrimidine; Diorganotin(IV); Mossbauer; DFT calculations; Antimicrobial activityAdductMossbauerInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundchemistryOctahedronMössbauer spectroscopyMaterials ChemistryTriazolopyrimidinePhysical and Theoretical ChemistryTinDiorganotin(IV)Journal of Organometallic Chemistry
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Tin( II ) and Lead( II ) 4‐Acyl‐5‐pyrazolonates: Synthesis, Spectroscopic and X‐ray Structural Characterization

2004

Novel tin(II) β-diketonate Sn(Q)2 complexes [HQ = 1-R1-3-R3-4-R4(C=O)-pyrazol-5-one; HQC: R1 = Ph, R3 = Me, R4 = Cy; HQS: R1 = Ph, R3 = Me, R4 = CHPh2; HQL: R1 = Ph, R3 = Me, R4 = CH2Ph; HQT: R1 = Ph, R3 = Me, R4 = CH2tBu; HQE: R1 = Ph, R3 = Me, R4 = Et; HQB: R1 = Ph, R3 = Me, R4 = tBu; HQW: R1 = Ph, R3 = Me, R4 = p-(tBu)Ph; HQR: R1 = Ph, R3 = Me, R4 = p-[(CH2)5CH3]Ph; HQN: R1 = p-NO2Ph, R3 = Me, R4 = Ph; HQM: R1 = Me, R3 = Me, R4 = Ph; HQD: R1 = Me, R3 = Me, R4 = Me; HQP: R1 = Ph, R3 = Ph, R4 = Ph; HQG: R1 = Ph, R3 = Ph, R4 = Me; HQF: R1 = p-CF3Ph, R3 = Me, R4 = Ph; HQH: R1 = p-CF3Ph, R3 = Me, R4 = Me] have been isolated and characterized by single-crystal X-ray diffraction analyses, IR, 1…

Steric effectsStereochemistryChemistryCoordination numberCrystal structureNuclear magnetic resonance spectroscopyInorganic ChemistryMetalCrystallographyMolecular geometryCovalent radiusvisual_artvisual_art.visual_art_mediumReactivity (chemistry)European Journal of Inorganic Chemistry
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Crystal structure of ethyl 2-(di-eth-oxy-phosphor-yl)-2-(2,3,4-tri-meth-oxy-phen-yl)acetate.

2014

The title compound, C17H27O8P, was prepared by Michaelis–Arbuzov reaction of ethyl 2-bromo-2-(2,3,4-trimethoxyphenyl)acetate and triethyl phosphite. Such compounds rarely crystallize, but single crystals were recovered after the initial oil was left for approximately 10 years. The bond angle of thesp3-hybridized C atom connecting the benzene derivative with the phospho unit is widened marginally [112.5 (2)°]. The terminal P—O bond length of 1.464 (2) Å clearly indicates a double bond, whereas the two O atoms of the ethoxy groups connected to the phosphorous atom have bond lengths of 1.580 (2) Å and 1.581 (3) Å. The three methoxy groups emerge out of the benzene-ring plane due to steric hind…

Steric effectschemistry.chemical_classificationcrystal structureCrystallographyMichaelis–Arbuzov reactionDouble bondChemistryHydrogen bondGeneral ChemistryCrystal structurephosphonoacetateCondensed Matter PhysicsBioinformaticsData ReportsBond lengthCrystalCrystallographyMolecular geometryQD901-999hydrogen bondsMichaelis–Arbuzov reactionGeneral Materials Sciencenon-merohedral twinActa crystallographica. Section E, Structure reports online
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Crystal structure of N-(tert-butoxycarbonyl)phenylalanyldehydroalanine isopropyl ester (Boc–Phe–ΔAla–OiPr)

2014

In the crystal structure of the de­hydro­dipeptide (Boc-Phe-ΔAla-OiPr), the mol­ecule has a trans configuration of the N-methyl­amide group. Its geometry is different from saturated peptides but is in excellent agreement with other de­hydro­alanine compounds. In the crystal, an N—H⋯O hydrogen bond links the mol­ecules in a herringbone packing arrangement.

Steric effectsde­hydro­alaninecrystal structurede­hydro peptidesCrystal structureResearch Communicationslcsh:Chemistrychemistry.chemical_compoundDehydroalanineαβ-dehydroamino acidsPeptide bondMoietyGeneral Materials ScienceHydrogen bond[alpha]General Chemistrydehydroalaninedehydro peptidesCondensed Matter Physicsherringbone packing[beta]-de­hydro­amino acidsCrystallographyMolecular geometrychemistrylcsh:QD1-999αβ-de­hydro­amino acidsIsopropylActa Crystallographica Section E
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Halogen...halogen interactions in pressure-frozen ortho- and meta-dichlorobenzene isomers.

2007

Isomers 1,2-dichlorobenzene (o-DCB) and 1,3-dichlorobenzene (m-DCB) were high-pressure frozen in-situ in a Merrill–Bassett diamond–anvil cell and their structures determined at room temperature and at 0.18 (5) GPa for o-DCB, and 0.17 (5) GPa for m-DCB by single-crystal X-ray diffraction. The patterns of halogen...halogen intermolecular interactions in these structures can be considered to be the main cohesive forces responsible for the molecular arrangements in these crystals. The molecular packing of dichlorobenzene isomers, including three polymorphs of 1,4-dichlorobenzene (p-DCB), have been compared and relations between their molecular symmetry, packing arrangements, intermolecular inte…

Steric effectspressure-crystallization methodhigh-pressure crystal structureStereochemistryChemistryIntermolecular forcehalogen...halogen intermolecular interactionsstructure-property relationsGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyDichlorobenzeneCrystallographyMolecular geometryMolecular symmetryMelting pointMoleculeActa crystallographica. Section B, Structural science
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