Search results for "force"

showing 10 items of 3423 documents

A new tetranuclear copper(I) complex based on allyl(5-phenyl-1,3,4-thiadiazol-2-yl)azanide ligand: Synthesis and structural characterization

2015

Abstract By means of alternating current electrochemical technique a new tetranuclear crystalline copper(I) complex [Cu I 4 ( L − ) 4 ] ( L −  – allyl(5-phenyl-1,3,4-thiadiazol-2-yl)azanide ion) has been obtained and characterized by X-ray single crystal diffraction ( Sp. gr. I 4 1 / a ) and Raman spectroscopy. The metal center adopts linear arrangement, composed of one thiadiazole N atom from the one L − anion and one azanide N atom of the other L − ligand. A bridged Cu atoms stitch four L − ligands into the firstly observed tetranuclear copper(I) azanide complex with intramolecular Cu(I)⋯Cu(I) interactions at the distance of 2.7451(6) A. Molecular structure and Raman spectrum of the compo…

Stereochemistrychemistry.chemical_elementthiadiazoleElectrochemistryDFTAnalytical ChemistryInorganic ChemistryMetalsymbols.namesakeraman spectroscopyMoleculeta116SpectroscopyBasis setLigandChemistryOrganic Chemistryac-electrochemical techniquetetranuclear complexCopperCrystallographyvisual_artIntramolecular forcevisual_art.visual_art_mediumsymbolsRaman spectroscopyCopper(I)Journal of Molecular Structure
researchProduct

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
researchProduct

Iron(III) bis(pyrazol-1-yl)acetate based decanuclear metallacycles: synthesis, structure, magnetic properties and DFT calculations

2016

The synthesis, structural aspects, magnetic interpretation and theoretical rationalizations for a new member of the ferric wheel family, a decanuclear iron(III) complex with the formula [Fe10(bdtbpza)10(μ2-OCH3)20] (1), featuring the N,N,O tridentate bis(3,5-di-tert-butylpyrazol-1-yl)acetate ligand, are reported. The influence of the steric effect on both the core geometry and coordination mode is observed. Temperature dependent (2.0–300 K range) magnetic susceptibility studies carried out on complexes 1 established unequivocally antiferromagnetic (AF) interactions between high-spin iron(III) centers (S = 5/2), leading to a ground state S = 0. The mechanism of AF intramolecular coupling was…

Steric effects010405 organic chemistryChemistryStereochemistryLigand010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographyiron complexesIntramolecular forcemetallacyclesmedicineFerricAntiferromagnetismacetate ligandsmagnetic propertiesGround stateta116density functional theoryMagnetic interpretationmedicine.drugDalton Transactions
researchProduct

Stability of Dinuclear Phosphane Palladium(III) Complexes: A DFT Approach

2018

Computational density functional theory studies have been carried out for the dinuclear ortho-metalated palladium(III) compounds [Pd2{μ-(C6H4)PPh2}2{μ-(X1-X2)}2Cl2]. These studies have shown that the electronic and steric properties of the auxiliary ligands (X1-X2 = bridging (carboxylato) or chelating (phenolato/acetylacetonato) O,O-donor ligands, bridging N,N-donor ligands (triazenido/formamidinato/pyrazolato), and bridging N,S-donor ligands) lead to systematic trends in their stability, highlighting that (a) the electronic nature of the donor atoms trans to the P has a clear trend, the replacement of hard donor atoms (O, N) by softer S donors generally reducing the stability of the compou…

Steric effects010405 organic chemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographychemistryIntramolecular forceDensity functional theoryChelationPhysical and Theoretical ChemistryPalladiumOrganometallics
researchProduct

Overcoming Steric Hindrance in Aryl‐Aryl Homocoupling via On‐Surface Copolymerization

2019

On-surface synthesis is a unique tool for growing low-dimensional carbon nanomaterials with precise structural control down to the atomic level. This novel approach relies on carefully designed precursor molecules, which are deposited on suitable substrates and activated to ultimately form the desired nanostructures. One of the most applied reactions to covalently interlink molecular precursors is dehalogenative aryl-aryl coupling. Despite the versatility of this approach, many unsuccessful attempts are also known, most of them associated to the poor capability of the activated precursors to couple to each other. Such failure is often related to the steric hindrance between reactants, which…

Steric effectsArylIntermolecular force02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesNanomaterialschemistry.chemical_compoundAdsorptionchemistryCovalent bond540 ChemistryCopolymer570 Life sciences; biologyPhysical and Theoretical Chemistry0210 nano-technologyChemPhysChem
researchProduct

Photochemical Generation of Cyclophanes from 1,3,5-Trisubstituted Benzenes with Chalcone Chromophores

2007

(E,E,E)-1,3,5-Tricinnamoylbenzene (7a) photodimerizes in solution to the [4.4.4](1,3,5)cyclophane 8a. The process consists of three consecutive steps in which cisoid enone conformations of 7a react in regio- and stereoselective anti-head-to-head cycloadditions. (E,E,E)-1,3,5-Tris(3-oxo-3-phenylpropenyl)benzene (13a), an isomer of 7 with reversed enone units, shows a single [2π+2π] cycloaddition of the same type. Due to steric reasons, it is afterwards not capable of intramolecular processes and oligomerizes by intermolecular photocycloadditions. Photolyses in the crystalline state yield dimers by topochemically controlled syn-head-to-tail processes (7a → 10a, 13a → 15a). An efficient dimeri…

Steric effectsChalconeOlefin fiberChemistryStereochemistryOrganic ChemistryRegioselectivityPhotochemistryCycloadditionchemistry.chemical_compoundIntramolecular forcePhysical and Theoretical ChemistryEnoneCyclophaneEuropean Journal of Organic Chemistry
researchProduct

Dinitrogen complexation with main group radicals

2011

In this report we present data from hyperfine sublevel correlation spectroscopy (HYSCORE), an electron paramagnetic resonance (EPR) spectroscopic technique, that reveals weak but distinct interactions between several main group element radicals and physically dissolved dinitrogen in solution. These interactions are the basis for a well-defined coordination of N2 to the paramagnetic centers. The complexes formed are primarily of the van der Waals-type but also feature a non-negligible orbital overlap between dinitrogen and the radicals' SOMO. Our spectroscopic findings are strongly supported by experiments with isotope-labeled 15N2, spectral simulations and quantum chemical and density funct…

Steric effectsChemistryGeneral ChemistryOrbital overlapPhotochemistrylaw.inventionsymbols.namesakeMain group elementComputational chemistryPolarizabilitylawsymbolsDensity functional theoryPhysics::Chemical Physicsvan der Waals forceElectron paramagnetic resonanceHyperfine structureChem. Sci.
researchProduct

Weak intermolecular interactions promote blue luminescence of protonated 2,2′-dipyridylamine salts

2014

In this work we demonstrate that protonation and π-stacking can be exploited to convert non-luminescent 2,2′-dipyridylamine into blue-emitting derivatives. We have synthesized a series of luminescent 2,2′-dipyridylamine (dpa) salts, i.e., (dpaH)X·nSolv (dpa = 2,2′-dipyridylamine, X = HF2, n = 0.5, Solv = H2O 1; X = Cl, n = 2, Solv = H2O 2; X = Br, n = 2, Solv = H2O 3; X = I n = 1, Solv = H2O 4a; X = I n = 1, Solv = CHCl34b), (dpaH)2[SiF6]·H2O 5 and (dpaH)X (X = I36; SbF67; BF48) and characterized their emission properties, both in the solid-state and in solution. To rationalize our observations and relate the luminescence properties to the structure in the solid state and in solution, we ha…

Steric effectsChemistryHydrogen bondIntermolecular forceSolid-stateProtonationGeneral ChemistryConical intersectionCrystallographyComputational chemistryMaterials ChemistryAb initio computationsLuminescenceta116J. Mater. Chem. C
researchProduct

Chemistry of density : extension and structural origin of Carnelley's rule in chloroethanes

2012

Low-density liquids and solids, with all intermolecular contacts longer than the sum of van der Waals radii, are formed by all ethanes chlorinated at one locant: CH2ClCH3, CHCl2CH3 and CCl3CH3. The concepts of molecular symmetry described by Carnelley and that of point groups have been compared. Carnelley's rule, when applied to liquid and solid chloroethanes clearly reveals the density dependence on the presence of intermolecular Cl⋯Cl and H⋯Cl short contacts, or their absence due to steric hindrances of overcrowded substituents. At 2.62 GPa, CH2ClCH3 freezes directly into phase II, with molecules arranged into layers with short Cl⋯Cl, H⋯Cl and H⋯H contacts. Only for CH2ClCH3, both the low…

Steric effectsChemistryIntermolecular forceGeneral ChemistryCondensed Matter PhysicsPoint groupLocantsymbols.namesakeComputational chemistryChemical physicsPhase (matter)Molecular symmetrysymbolsMoleculeGeneral Materials ScienceVan der Waals radiusCrystEngComm
researchProduct

Solid State Luminescence Enhancement in π-Conjugated Materials: Unraveling the Mechanism beyond the Framework of AIE/AIEE

2017

Solid state luminescence enhancement (SLE) of conjugated organic materials has had a great impact in materials science, but a deep understanding has been rather limited to date. Here, we investigate a prototype example of SLE materials, cyano-substituted distyrylbenzene (DCS), by varying systematically and subtly the substitution pattern (inter alia of the position of the cyano-substituent) to give largely different photoresponse in fluid and solid solution as well in the crystalline state. The combination of quantitative (ultra)fast optical spectroscopic techniques, appropriate quantum-chemical methods, and structural (X-ray) data allows us to elucidate and rationalize all details of the S…

Steric effectsChemistryIntermolecular forceSolid-stateNanotechnology02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyChemical physicsMechanism (philosophy)Radiative transferPhysical and Theoretical Chemistry0210 nano-technologyLuminescenceSolid solutionThe Journal of Physical Chemistry C
researchProduct