Search results for "Configuration"

showing 10 items of 601 documents

Binding and isomerization energies for the Cu/CN and Cu(I)CN interactions

1993

Abstract Binding and isomerization energies of the CuCN, CuNC, CuCN+, and CuNC+ systems were investigated by means of a multireference CI perturbatively selected, MRCI-PS approach. The inclusion of the main dynamical correlation effects are evaluated. The binding energies for CuCN and CuNC are 4.37 and 4.03 eV, respectively, and those for CuCN+ and CuNC+ are 0.08 and 1.61 eV. Calculated isomerization energies are 7.86 and 35.98 kcal/mol for CuCN and Cu(I)CN isomerizations, respectively.

chemistry.chemical_classificationElectronic correlationBinding energyGaussian orbitalGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyCrystallographychemistryComputational chemistryElectron affinityPhysical and Theoretical ChemistryInorganic compoundIsomerizationChemical Physics
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Dissociation energies within selected configuration interaction and perturbation theory

1993

Abstract Selected configuration interaction (CI) calculations and second-order perturbational theory are used to truncate systematically multireference single and double excitation CI (MRCI) expansions in the calculation of the bond dissociation energies of several systems like the single-bonded LiF molecule or the multiple-bonded N2, NO and O2 diatomic systems. The method is extended to compute the CH bond dissociation energy ofethene C2H4. It is shown how the proposed scheme (perturbation-selected MRCI (MRCI-PS)) is able to reproduce the accuracy of complete MRCI expansions with only a small number of configurations variationally evaluated.

chemistry.chemical_classificationElectronic correlationConfiguration interactionCondensed Matter PhysicsBiochemistryBond-dissociation energyDiatomic moleculeMolecular physicsDissociation (chemistry)chemistryComputational chemistryMoleculePhysical and Theoretical ChemistryInorganic compoundExcitationJournal of Molecular Structure: THEOCHEM
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High Yield Syntheses of Stable, Singly Bonded Pd26+ Compounds

2006

A general method for the syntheses of dipalladium compounds having a singly bonded Pd26+ core and the formula R,S-cis-Pd2(C6H4PPh2)2(O2CR)2Cl2 is described. When the alkyl group in the carboxylate ligands is an electron donating group, the compounds are stable and the yields high. The Pd-Pd distances for the diamagnetic compounds with R = CF3 and CMe3 are 2.5434(4) and 2.5241(9) A, respectively. Calculations at the DFT level suggest that the electronic configuration is sigma2pi4delta2delta*2pi*4. These represent rare examples of palladium(III) compounds.

chemistry.chemical_classificationGeneral methodStereochemistrychemistry.chemical_elementGeneral ChemistryBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryGroup (periodic table)Yield (chemistry)DiamagnetismCarboxylateElectron configurationAlkylPalladiumJournal of the American Chemical Society
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Stereospecific CC-bond formation with rabbit muscle aldolase - A chemoenzymatic synthesis of (+)-exo-brevicomin

1990

Abstract (+)-(1S,5R,7S)-Exo-brevicomin 9, a sex pheromone of the western pine bark beetle, is synthesized using an aldol reaction catalyzed by fructose-1,6-diphosphate aldolase (EC 4.1.2.13) from rabbit muscle as the key step by which the absolute configuration of the target is established.

chemistry.chemical_classificationKetonebiologyStereochemistryOrganic ChemistryAldolase AAbsolute configurationFructose-bisphosphate aldolasecomplex mixturesBiochemistryEnzyme catalysisStereospecificitychemistryAldol reactionDrug Discoverybiology.proteinAldol condensationTetrahedron Letters
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The role of dislocations in the solid-state polymerization of monomers having conjugated triple bonds: A study of 2,4-hexadiyne-1,6-diol bis(p-toluen…

1975

The crystal structure of the monomer bis(p-toluene sulfonate) ester of 2,4-hexadiyne-1,6-diol (pT) is conducive from the viewpoint of both the separation distances and molecular configuration, to polymerization, irrespective of whether initiation is thermal, photochemical, or mechanical. The dislocations present in the monomer and polymer structures have been characterized by employing optical microscopic techniques. The slip system (102)[010] is found to be present in both monomer and polymer crystals but the (010)[001] system is found only in the monomer. On this basis a crystal structure for the monomer is proposed based on existing crystallographic information relating to the structure …

chemistry.chemical_classificationMaterials scienceGeneral EngineeringNucleationPolymerCrystal structureMolecular configurationchemistry.chemical_compoundMonomerSulfonateChain-growth polymerizationchemistryPolymerizationPolymer chemistryJournal of Polymer Science: Polymer Physics Edition
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Ligand design for multidimensional magnetic materials: a metallosupramolecular perspective.

2008

The aim and scope of this review is to show the general validity of the ‘complex-as-ligand’ approach for the rational design of metallosupramolecular assemblies of increasing structural and magnetic complexity. This is illustrated herein on the basis of our recent studies on oxamato complexes with transition metal ions looking for the limits of the research avenue opened by Kahn's pioneering research twenty years ago. The use as building blocks of mono-, di- and trinuclear metal complexes with a novel family of aromatic polyoxamato ligands allowed us to move further in the coordination chemistry-based approach to high-nuclearity coordination compounds and high-dimensionality coordination po…

chemistry.chemical_classificationModels MolecularMolecular StructureChemistryMagnetismLigandMacromolecular SubstancesRational designMolecular electronicsNanotechnologyBridging ligandCrystallography X-RayLigandsCoordination complexInorganic ChemistryMagneticsMetals HeavyOrganometallic CompoundsMoleculeElectron configurationDalton transactions (Cambridge, England : 2003)
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I. Glass Transition. Theoretical concepts on the glass transition of polymers and their test by computer simulation

1996

Various organic molecules, in particular polymers, are extremely good glass formers and allow the study of supercooled melts near the glass transition in metastable equilibrium. Theories of the glass transition imply such an equilibrium (e.g. mode-coupling theory, or Gibbs-di Marzio theory) and can hence be tested in these systems. Simplified lattice models for polymer melts (e.g. the bond fluctuation model) have been developed that can very efficiently be studied by Monte-Carlo simulation, and although they fail to accurately describe the local structure, they describe many features of the experiments very well. In this model, the mechanism of the glass transition is a competition between …

chemistry.chemical_classificationPhase transitionMaterials scienceGeneral Chemical Engineeringmedia_common.quotation_subjectConfiguration entropyFrustrationThermodynamicsPolymerCondensed Matter::Soft Condensed MatterchemistryGravitational singularitySupercoolingGlass transitionmedia_commonEntropy (order and disorder)Berichte der Bunsengesellschaft für physikalische Chemie
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Glass transition of polymer melts: Test of theoretical concepts by computer simulation.

2003

Abstract Polymers are good glass formers and allow for the study of melts near the glass transition in (meta-)stable equilibrium. Theories of the glass transition imply such an equilibrium and can, hence, be tested by the study of polymer melts. After a brief summary of the basic experimental facts about the glass transition in polymers, the main theoretical concepts are reviewed: mode coupling theory (MCT), entropy theory, free-volume theory, the idea of a growing length describing the size of cooperative regions, etc. Then, two basic coarse-grained models of polymers are described, which have been developed aiming at a test of these concepts. The first model is the bond-fluctuation model …

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodConfiguration entropy02 engineering and technologySurfaces and InterfacesPolymer021001 nanoscience & nanotechnology01 natural sciencesCondensed Matter::Soft Condensed MatterMolecular dynamics0103 physical sciencesMode couplingMaterials ChemistryCeramics and CompositesEntropy (information theory)Kinetic Monte CarloStatistical physics010306 general physics0210 nano-technologyGlass transition[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
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Monte carlo simulation of the glass transition of polymer melts

2007

The bond fluctuation model of polymer melts is presented as a reasonable compromise between simulation efficiency and realistic chemical detail. It is shown that inclusion of a potential energy that depends on the length of the effective bonds connecting the effective monomers easily creates a conflict between configurational entropy of dense packing and the energetic tendency of the bonds to stretch. This competition leads to a glass transition of the model, which very well describes many features of real systems.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodConfiguration entropyThermodynamicsPolymerPotential energyCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerchemistryGlass transitionSupercoolingBond fluctuation model
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Diastereoselective formation of highly functionalised α-substituted amino acid derivatives via aldol addition

2005

Abstract Highly diastereoselective aldol additions of (2 R ,4 S )-3- tert -butyl 4-methyl 2- tert -butyloxazolidine-3,4-dicarboxylate ( 1 ) are reported. The utility of the highly substituted oxazolidines of type 1 for diastereoselective α-addition of the fully protected amino acid l -serine with achiral and chiral carbonyl compounds is demonstrated and the relative and absolute configuration of the aldol products are discussed on the basis of NOESY data and solid state structures of selected examples. The aldol products represent highly useful intermediates in the syntheses of sphingosine-related metabolites.

chemistry.chemical_classificationStereochemistryOrganic ChemistryAbsolute configurationSolid-stateAnalytical ChemistryAmino acidInorganic ChemistrySerineAldol reactionchemistrySubstituted Amino AcidTwo-dimensional nuclear magnetic resonance spectroscopySpectroscopyJournal of Molecular Structure
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