Search results for "120"

showing 10 items of 581 documents

Interaction of Novel Metal Complexes with DNA: Synthetic and Structural Aspects

2009

Metal ions bind to nucleic acids at various positions. This binding can be modulated by using metal complexes with appropriate ligands. Novel mono- and especially dinuclear metal complexes could be a powerful tool to detect rare, but still physiologically relevant, forms of DNA, e.g. the left-handed Z-DNA. In this review, our recent research activities in this area of bioinorganic chemistry are summarized. A special emphasis is laid on the synthetic challenges that arose upon the synthesis of the polyamine ligands. Further, some rather unusual approaches to elucidate the solution structure of copper bound to guanosine monophosphate with the help of pulsed EPR techniques like ENDOR and HYSC…

10120 Department of ChemistryMono- and dinuclear metal complexesMetal ions in aqueous solutionand dinuclear metal complexes1600 General ChemistrydnaBioinorganic chemistryZ-DNAMetalchemistry.chemical_compoundMono- and Dinuclear Metal ComplexeGuanosine monophosphate540 ChemistryQD1-999Pulsed EPRCrystal structureBioinorganic chemistryGeneral MedicineGeneral ChemistryZ-DNACombinatorial chemistrySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Chemistrychemistryvisual_artCrystal structuresNucleic acidvisual_art.visual_art_mediumMonoSynthetic ChemistryDNAZ
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Angular Trapping of Anisometric Nano-Objects in a Fluid

2012

We demonstrate the ability to trap, levitate, and orient single anisometric nanoscale objects with high angular precision in a fluid. An electrostatic fluidic trap confines a spherical object at a spatial location defined by the minimum of the electrostatic system free energy. For an anisometric object and a potential well lacking angular symmetry, the system free energy can further strongly depend on the object's orientation in the trap. Engineering the morphology of the trap thus enables precise spatial and angular confinement of a single levitating nano-object, and the process can be massively parallelized. Since the physics of the trap depends strongly on the surface charge of the objec…

10120 Department of ChemistryOptics and Photonics3104 Condensed Matter PhysicsSilverMaterials scienceMacromolecular SubstancesSurface PropertiesStatic Electricity2210 Mechanical EngineeringMetal Nanoparticles1600 General ChemistryBioengineeringTrap (computing)OpticsOrientation (geometry)540 ChemistryNano-ElectrochemistryNanotechnologyScattering RadiationGeneral Materials ScienceFluidicsSurface chargeParticle Size1502 Bioengineeringbusiness.industryPhysicsMechanical EngineeringElectrostatic unitsDNAGeneral ChemistryCondensed Matter Physics2500 General Materials ScienceSymmetry (physics)KineticsHydrodynamicsLevitationAnisotropybusinessNano Letters
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Efficient Linear-Scaling Density Functional Theory for Molecular Systems

2013

Despite recent progress in linear scaling (LS) density function theory (DFT), the computational cost of the existing LS methods remains too high for a widespread adoption at present. In this work, we exploit nonorthogonal localized molecular orbitals to develop a series of LS methods for molecular systems with a low computational overhead. High efficiency of the proposed methods is achieved with a new robust two-stage variational procedure or by replacing the optimization altogether with an accurate nonself-consistent approach. We demonstrate that, even for challenging condensed-phase systems, the implemented LS methods are capable of extending the range of accurate DFT simulations to molec…

10120 Department of ChemistryWork (thermodynamics)Mathematical optimization010304 chemical physicsSeries (mathematics)Computer scienceLocalized molecular orbitalsMolecular systems01 natural sciencesComputer Science ApplicationsRange (mathematics)0103 physical sciences540 ChemistryLinear scale1706 Computer Science ApplicationsDensity functional theoryPhysical and Theoretical Chemistry010306 general physics1606 Physical and Theoretical ChemistryAlgorithmOrder of magnitude
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Crystal and solution structures of di-n-butyltin(IV) complexes of 5-[(E)-2-(4-methoxyphenyl)-1-diazenyl]quinolin-8-ol and benzoic acid derivatives: E…

2009

Abstract Reactions of nBu2SnCl(L1) (1), where L1 = acid residue of 5-[(E)-2-(4-methoxyphenyl)-1-diazenyl]quinolin-8-ol, with various substituted benzoic acids in refluxing toluene, in the presence of triethylamine, yielded dimeric mixed ligand di-n-butyltin(IV) complexes of composition [nBu2Sn(L1)(L2–6)]2 where L2 = benzene carboxylate (2), L3 = 2-[(E)-2-(2-hydroxy-5-methylphenyl)-1-diazenyl]benzoate (3), L4 = 5-[(E)-2-(4-methylphenyl)-1-diazenyl]-2-hydroxybenzoate (4), L5 = 2-{(E)-4-hydroxy-3-[(E)-4-chlorophenyliminomethyl]-phenyldiazenyl}benzoate (5) and L6 = 2-[(E)-(3-formyl-4-hydroxyphenyl)-diazenyl]benzoate (6). All complexes (1–6) have been characterized by elemental analyses, IR, 1H,…

10120 Department of Chemistry[(E)81303 Biochemistry5DenticityStereochemistry12Crystal structuredinBiochemistrybutyltin(IV) complexes(4Inorganic Chemistrychemistry.chemical_compoundPentagonal bipyramidal molecular geometry540 ChemistryMaterials ChemistryCarboxylatePhysical and Theoretical Chemistry2505 Materials ChemistryCoordination geometryXmixed ligandsol1604 Inorganic ChemistryChemistryCrystal structurebenzoic acidOrganic Chemistry5-[(E)-2-(4-methoxyphenyl)-1- diazenyl]quinolin-8-ol Di-n-butyltin(IV) complexes Benzoic acid Mixed ligands Solution and solid-state tin NMR Crystal structureNuclear magnetic resonance spectroscopysolution and solid state tinNMRBond lengthTrigonal bipyramidal molecular geometryCrystallographydiazenyl]quinolinmethoxyphenyl)Settore CHIM/03 - Chimica Generale E Inorganica1606 Physical and Theoretical Chemistry1605 Organic Chemistry
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Desulfurization and ring opening of thiirane induced by tantalocene trihydride complexes: Synthesis, reactivity and X-ray structure of Cp′2Ta(=S)(S-i…

1999

The reaction of the tantalocene trihydride complexes Cp′ 2 TaH 3 1 (Cp′= η 5 -C 5 H 4 t Bu) or Cp″CpTaH 3 1′ (Cp″= η 5 -C 5 H 2 -1,2-Me 2 -4- t Bu) with propylene sulfide was found to proceed via an unprecedented sulfur transfer and regioselective ring opening reaction at once to yield sulfido-thiolato tantalocene complexes Cp′ 2 Ta(S)(S- i Pr) 2a whose structure has been determined by X-ray crystallography or Cp″CpTa(S)(S- i Pr) 2′a . Complex 1 reacts with ethylene sulfide to give Cp′ 2 Ta(S)(S–Et) 2b . The reactivity of 2a towards a variety of electrophilic moities has been investigated: protonation (with HBF 4 ) and alkylation (with MeI) reactions occur at the terminal sulfur ligand, …

10120 Department of Chemistrychemistry.chemical_classification1303 BiochemistryEthyleneSulfide1604 Inorganic ChemistryStereochemistryOrganic ChemistryRegioselectivityProtonationCrystal structureAlkylationBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryThiirane540 ChemistryElectrophileMaterials ChemistryPhysical and Theoretical Chemistry1606 Physical and Theoretical Chemistry2505 Materials Chemistry1605 Organic Chemistry
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Reactions of the hydrofluoroborate salts of open-chain analogues of Reissert compounds with some α,β-ethylenic esters

1999

The reaction of the hydrofluoroborate salt of an open-chain analogue of a Reissert compound with some α,β-ethylenic esters does not give a [4 + 2] cycloadduct, as previously described in the case of ethyl acrylate. The reaction starts with a 1,3-dipolar cycloaddition of a munchnone imine 5c, d. The [3 + 2] cycloadducts 13 evolve via a rearrangement–condensation sequence to give a substituted 2-pyridone derivative 18 or 19. The proposed mechanism has been verified by the isolation and structural X-ray analysis of some compounds of the reaction sequence.

10120 Department of Chemistrychemistry.chemical_classificationOrganic ChemistryImineSalt (chemistry)Azomethine ylideSequence (biology)Medicinal chemistryCycloadditionchemistry.chemical_compoundchemistry540 Chemistry13-Dipolar cycloadditionEthyl acrylatePhysical and Theoretical Chemistry1606 Physical and Theoretical ChemistryDerivative (chemistry)1605 Organic Chemistry
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Synthesis and stereochemical studies of 2-substituted thiazolidine-4-carboxamide derivatives

2000

A series of new 2-substituted thiazolidine-4-carboxamide derivatives which have potentially useful immunological properties, have been synthesized in a stereoselective manner by coupling 2-subsituted thiazolidine-4-carboxylic acids with amines or amino esters. The structure of these compounds was established by combination of NMR methods and by X-ray analysis.

10120 Department of Chemistrychemistry.chemical_compoundAmino esterschemistrymedicine.drug_classStereochemistryOrganic ChemistryThiazolidine540 ChemistrymedicineCarboxamideStereoselectivity1605 Organic Chemistry
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Influence of the exchange and correlation functional on the structure of amorphous InSb and In3SbTe2 compounds

2016

We have investigated the structural, vibrational, and electronic properties of the amorphous phase of InSb and In3SbTe2 compounds of interest for applications in phase change non-volatile memories. Models of the amorphous phase have been generated by quenching from the melt by molecular dynamics simulations based on density functional theory. In particular, we have studied the dependence of the structural properties on the choice of the exchange-correlation functional. It turns out that the use of the Becke-Lee-Yang-Parr functional provides models with a much larger fraction of In atoms in a tetrahedral bonding geometry with respect to previous results obtained with the most commonly used P…

10120 Department of Chemistrynon-volatile memoryYield (engineering)Theory of Condensed MatterGeneral Physics and Astronomy02 engineering and technologyElectronic structure01 natural sciencesMolecular dynamicsComputational chemistry540 Chemistry0103 physical sciencesPhysical and Theoretical Chemistry010306 general physicsamorphous materialFIS/03 - FISICA DELLA MATERIAQuenchingChemistry021001 nanoscience & nanotechnologyelectronic structure3100 General Physics and AstronomyAmorphous solidab-initio simulationChemical physicsMolecular vibrationTetrahedronDensity functional theory1606 Physical and Theoretical Chemistry0210 nano-technologyphase change material
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Wheelchair half-marathon and marathon performance: The ‘Oita International Wheelchair Marathon’ 1983-2011

2013

Knechtle, B. & Lepers, R. (2013). Wheelchair half-marathon and marathon performance ‐ the ‘Oita International Wheelchair Marathon’ 1983-2011. J. Hum. Sport Exerc., 8(4), pp.974-985. We compared participation and performance trends of individuals with disabilities competing in the half- and full-marathon in the ‘Oita International Wheelchair Marathon’ from 1981 to 2011. The performance times decreased during the 1980’s until the middle 1990’s and stabilized thereafter for both half-marathoners and marathoners. The mean top five overall finishers times were 0:52±0:07 h:min for half-marathoners and 1:36 ±0:11 h:min for marathoners, respectively. The mean age of the finishers increased signific…

11035 Institute of General PracticeAge effectmedicine.medical_specialty610 Medicine & healthPhysical Therapy Sports Therapy and RehabilitationSpinal cord injuryEnduranceWheelchairPhysical medicine and rehabilitationHumEducación Física y DeportivaMedicine3612 Physical Therapy Sports Therapy and Rehabilitationlcsh:Sports medicineSpinal cord injurybiologyIndividuals with disabilitybusiness.industryAthletesMean agebiology.organism_classificationmedicine.diseaseAging athletesPhysical therapybusinesslcsh:RC1200-1245Journal of Human Sport and Exercise
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European dominance in multistage ultramarathons: an analysis of finisher rate and performance trends from 1992 to 2010

2013

Mohannad Abou Shoak,1 Beat Knechtle,1,2 Christoph Alexander Rüst,1 Romuald Lepers,3 Thomas Rosemann11Institute of General Practice and for Health Services Research, University of Zurich, Zurich, Switzerland; 2Gesundheitszentrum St Gallen, St Gallen, Switzerland; 3INSERM U1093, Faculty of Sport Sciences, University of Burgundy, Dijon, FranceBackground: Participation and performance trends regarding the nationality of ultraendurance athletes have been investigated in the triathlon, but not in running. The present study aimed to identify the countries in which multistage ultramarathons were held around the world and the nationalities of successful finishers.Methods: Finisher rates and…

11035 Institute of General PracticeFuture studiesOperations researchbusiness.industryrun610 Medicine & healthTotal fieldnationalitystagelanguage.human_languageultraenduranceGermanDominance (economics)languageNationalityMedicinelcsh:Sports medicinelcsh:RC1200-1245businessdistanceOpen Access Journal of Sports MedicineTourismDemographyOriginal ResearchOpen Access Journal of Sports Medicine
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