Search results for "TRIP"

showing 10 items of 2134 documents

Incommensurate nature of the multilayered molecular ferromagnetic metals based on bis(ethylenedithio)tetrathiafulvalene and bimetallic oxalate comple…

2004

The salt [ET]x[MnRh(ox)(3)].CH(2)Cl(2) (x = 2.526(1)) has been obtained and characterized. This paramagnetic metal is essentially isostructural to the ferromagnetic metal [ET]y[MnCr(ox)(3)].CH(2)Cl(2) (y approximately equal to 3) and provides a definite answer on the origin of the structural disorder present on such systems. As in the ferromagnetic analogue, this material shows high electrical conductivity at room temperature (13 S.cm(-1)) and metallic behavior.

ChemistryMineralogyOxalateInorganic ChemistryMetalParamagnetismchemistry.chemical_compoundCrystallographyFerromagnetismElectrical resistivity and conductivityvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryIsostructuralBimetallic stripTetrathiafulvaleneInorganic chemistry
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Recent Approaches for Chemical Speciation and Analysis by Electrospray Ionization (ESI) Mass Spectrometry

2021

In these latest years, the chemical speciation of several species has been increasingly monitored and investigated by means of electrospray ionization mass spectrometry (ES-MS). This soft ionization technique is capable to gently take into the gas phase metal-ligand complexes and gather a wealth of information on their energetics, shape, and fragmentation pathways. For this reason, this technique is frequently chosen in a synergistic approach to investigate competitive ligand exchange-adsorptive other ways analyzed by cathodic stripping voltammetry (CLE-ACSV). ESI-MS analyses require a careful experimental design as they may be impacted by instrumental artifacts such as ESI adduct formation…

ChemistryMini ReviewElectrospray ionizationmetals speciation010401 analytical chemistryMetallomeelectrospray ionizationspeciation analysisGeneral Chemistry010402 general chemistryMass spectrometryTandem mass spectrometry01 natural sciencesmetallomics0104 chemical sciencesIonlcsh:ChemistryChemistryFragmentation (mass spectrometry)lcsh:QD1-999Computational chemistryIonizationCathodic stripping voltammetrymass spectrometryFrontiers in Chemistry
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Thermal stability and reaction of chalcogen-containing metallocenic compounds with elemental chalcogens

1989

Abstract Dissymmetrical four-membered bimetallocenacycles (t-BuC 5 H 4 ) 2 M(μ-S) 2 M′-(RC 5 H 4 ) 2 (M, M′ = Zr, Hf; R = H, t-Bu) have been prepared and found to give redistribution products in solution at 190°C; identification of these products shows that the reaction involves exclusive cleavage of a metal-sulfur bond. Elemental sulfur and selenium react with chalcogen-containing complexes. The reaction is shown to involve the introduction of chalcogenic species in place of the σ-ligands of the complex to give either four-membered bimetallic complexes or catenated pentachalcogen metallocenic compounds. Some examples of insertion of sulfur and tellurium into the zirconium-methyl bond are a…

ChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementBiochemistrySulfurInorganic ChemistryChalcogenPolymer chemistryMaterials ChemistryRedistribution (chemistry)Thermal stabilityPhysical and Theoretical ChemistryTelluriumBimetallic stripSeleniumJournal of Organometallic Chemistry
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Breaking the semi-quinoid structure: spin-switching from strongly coupled singlet to polarized triplet state.

2014

2,7-TMPNO (4,5,9,10-tetramethoxypyrene-2,7-bis(tert-butylnitroxide)) was found to exist in semi-quinoid form with unprecedented strong intramolecular magnetic exchange interaction of 2 J/kB = 1185 K operating over a distance of 10 A. Structural transformations with the activation energy of ΔEeq = 949 K were observed by varying the temperature, from more quinoid structure at low temperature to more biradicaloid structure at higher temperature. Moreover, this molecule undergoes a transient spin transition from singlet to polarized triplet state upon photoexcitation revealed by TREPR spectroscopy. The spin Hamiltonian parameters were determined to be S = 1, g = 2.0065, D = -0.0112 cm(-1), and …

ChemistryOrganic ChemistrySpin transitionGeneral ChemistryMolecular physicsCatalysislaw.inventionPhotoexcitationlawComputational chemistryIntramolecular forceSinglet stateTriplet stateElectron paramagnetic resonanceSpin (physics)SpectroscopyChemistry (Weinheim an der Bergstrasse, Germany)
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Synthese vonN-Glycopeptid-Partialstrukturen der Verknüpfungsregion sowohl der Transmembran-Neuraminidase eines Influenza-Virus als auch des Faktors B…

1989

Mit Hilfe der Schutzgruppenkombination Boc-Gruppe/Allylester und Acetylschutz im Kohlenhydratteil wurden die geschutzten N-Chitobiosyl-asparagin-peptide 12a und 14 synthetisiert, die der Verknupfungsregion des Faktors B des menschlichen Komplementsystems und einer Influenza-Virus-Neuraminidase entsprechen. Aus dem vollgeschutzten Glycopeptid 12a liesen sich der Allylester und die Acetylschutzgruppen simultan mit methanolischem Ammoniak und die Boc-Schutzgruppe mit wasserfreier Trifluoressigsaure ohne storende Nebenreaktionen entfernen. Versuche, die Boc-Gruppe aus an den Kohlenhydrat-Hydroxyfunktionen deblockierten Glycopeptiden abzulosen, fuhrten uberwiegend zur Spaltung der O-glycosidisch…

ChemistryOrganic ChemistryTripeptidePhysical and Theoretical ChemistryMolecular biologyLiebigs Annalen der Chemie
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First-principles calculations of oxygen interstitials in corundum: a site symmetry approach

2017

The authors are indebted to R. Vila, A. Popov and A. Lushchik for stimulating discussions. This work was carried out within the framework of the EUROfusion Consortium and received funding from the European Union’s Horizon 2020 Research and Innovation Programme under grant agreement 633053. The views and opinions expressed herein do not necessarily reflect those of the European Commission. Support from Latvian National Research Program IMIS2 (2014–2017) is also appreciated. Calculations were carried out using both the Marconi supercomputer system at the Computational Simulation Centre and the Computer Center of St. Petersburg State University.

ChemistryOxideGeneral Physics and AstronomyCharge (physics)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciences0104 chemical sciencesHybrid functionalCondensed Matter::Materials Sciencechemistry.chemical_compoundTriplet oxygenInterstitial defectAtom:NATURAL SCIENCES:Physics [Research Subject Categories]DumbbellSinglet statePhysical and Theoretical ChemistryAtomic physics0210 nano-technologyPhysical Chemistry Chemical Physics
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Raman spectroscopy and crystal-field split rotational states of photoproducts CO and H2 after dissociation of formaldehyde in solid argon.

2012

Raman signal is monitored after 248 nm photodissociation of formaldehyde in solid Ar at temperatures of 9-30 K. Rotational transitions J = 2 ← 0 for para-H(2) fragments and J = 3 ← 1 for ortho-H(2) are observed as sharp peaks at 347.2 cm(-1) and 578.3 cm(-1), respectively, which both are accompanied by a broader shoulder band that shows a split structure. The rovibrational spectrum of CO fragments has transitions at 2136.5 cm(-1), 2138.3 cm(-1), 2139.9 cm(-1), and 2149 cm(-1). To explain the observations, we performed adiabatic rotational potential calculations to simulate the Raman spectrum. The simulations indicate that the splitting of rotational transitions is a site effect, where H(2) …

ChemistryPhotodissociationGeneral Physics and AstronomyRotational–vibrational spectroscopyDissociation (chemistry)symbols.namesakeExcited statesymbolsMoleculeRotational spectroscopyPhysical and Theoretical ChemistryAtomic physicsTriplet stateRaman spectroscopyta116The Journal of chemical physics
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Relaxation Mechanisms of 5-Azacytosine.

2015

The photophysics and deactivation pathways of the noncanonical 5-azacytosine nucleobase were studied using the CASPT2//CASSCF protocol. One of the most significant differences with respect to the parent molecule cytosine is the presence of a dark (1)(nNπ*) excited state placed energetically below the bright excited state (1)(ππ*) at the Franck-Condon region. The main photoresponse of the system is a presumably efficient radiationless decay back to the original ground state, mediated by two accessible conical intersections involving a population transfer from the (1)(ππ*) and the (1)(nNπ*) states to the ground state. Therefore, a minor contribution of the triplet states in the photophysics o…

ChemistryRelaxation (NMR)NanotechnologyMolecular physicsComputer Science ApplicationsNucleobaseIntersystem crossingExcited stateNUCLEOSÍDEOSMoleculePhysical and Theoretical ChemistryTriplet stateGround stateQuantumJournal of chemical theory and computation
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Properties and performance of a quadrupole mass filter used for resonance ionization mass spectrometry

1998

Abstract The performance of commercial quadrupole mass spectrometers (QMS) with a number of imperfections, as compared to the ideal hyperbolic geometry, has been characterized using the computer simulation program simion 3d version 6.0. The analysis of simulated QMS geometries focuses primarily on modeling of the internal potential, the study of field deviations, and the influence of finite length on performance of the QMS. The computer simulation of ion trajectories in the QMS field yields predictions for optimum working conditions and provides estimates for the resolving power and the maximum isotopic abundance sensitivity. Experimental measurements that confirm these expectations are pre…

ChemistrySelected reaction monitoringAnalytical chemistryThermal ionization mass spectrometryCondensed Matter PhysicsMass spectrometryTriple quadrupole mass spectrometerComputational physicsSelected ion monitoringPhysical and Theoretical ChemistryTime-of-flight mass spectrometryInstrumentationQuadrupole mass analyzerSpectroscopyHybrid mass spectrometerInternational Journal of Mass Spectrometry
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A New Rhodium(III) Complex with a Tripodal Bis(imidazolylidene) Ligand. Synthesis and Catalytic Properties

2003

A new bis(imidazolylidene) tripodal ligand has been obtained by a simple method. The coordination of this ligand to Rh provides the first Rh(III) complex with a bis(carbene) ligand in a tripodal coordination, and its catalytic properties toward hydrogen transfer have been examined.

ChemistryStereochemistryLigandOrganic ChemistryHydrogen transferchemistry.chemical_elementRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundTripodal ligandPolymer chemistryPhysical and Theoretical ChemistryCarbeneOrganometallics
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