Search results for "PAIRS"

showing 10 items of 82 documents

Les systèmes de comportement du jeune enfant dans un groupe de pairs, aspects fonctionnels et ontogénétiques

1984

International audience

[SHS.ANTHRO-SE] Humanities and Social Sciences/Social Anthropology and ethnology[ SHS.ANTHRO-SE ] Humanities and Social Sciences/Social Anthropology and ethnologygroupe de pairsontogénétiquessystèmescomportementjeune enfant[SHS.ANTHRO-SE]Humanities and Social Sciences/Social Anthropology and ethnologyComputingMilieux_MISCELLANEOUSaspects fonctionnels
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L'adéquation entre Chambre des pairs et décentralisation sous la Monarchie de Juillet

2007

International audience

[SHS.DROIT]Humanities and Social Sciences/Law[SHS.DROIT] Humanities and Social Sciences/Lawchambre des pairsMonarchie de juillet[ SHS.DROIT ] Humanities and Social Sciences/LawComputingMilieux_MISCELLANEOUSdécentralisation
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Peer effects in the light of students interactions and the subjective dimensions of school experience

2011

This Thesis addresses the issue of peer-effects in the context of school. From analysis of a large database produced by a Chilean national study (SIMCE 2004), this work investigates the mechanisms through which pupils with different levels of scholastic, human and cultural capital influence each other. These influences seem present for a diverse range of school outcomes, including academic achievement. Drawing on the literature produced by different disciplinary approaches —sociology, economics, social psychology and education— the study focuses on ways of identifying and measuring peer-effects. The presence of subjective dimensions capable of reflecting, in part, the school experience of p…

[SHS.EDU]Humanities and Social Sciences/Education[SHS.EDU] Humanities and Social Sciences/EducationPeer-effectsModèles multiniveauxPratiques d'étude[ SHS.EDU ] Humanities and Social Sciences/EducationSégrégation socio-scolaireStudy practicesEntraideSchool well-beingFactorial analysisConcept de soi académiqueHierarchical modelsEffets de pairsPeer assistanceQuantile regressionChiliAcademic self-conceptChileRégression par quantilesBien-être à l'écoleSocial and academic segregationAnalyse factorielle
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On the tensor degree of finite groups

2013

We study the number of elements $x$ and $y$ of a finite group $G$ such that $x \otimes y= 1_{_{G \otimes G}}$ in the nonabelian tensor square $G \otimes G$ of $G$. This number, divided by $|G|^2$, is called the tensor degree of $G$ and has connection with the exterior degree, introduced few years ago in [P. Niroomand and R. Rezaei, On the exterior degree of finite groups, Comm. Algebra 39 (2011), 335--343]. The analysis of upper and lower bounds of the tensor degree allows us to find interesting structural restrictions for the whole group.

algebraic topologyFOS: MathematicsAlgebraic Topology (math.AT)Mathematics - CombinatoricsGroup Theory (math.GR)Combinatorics (math.CO)Mathematics - Algebraic TopologySettore MAT/03 - Geometria20D15 20J99 20D60 20C25Nonabelian tensor squareprobability of commuting pairsMathematics - Group Theory$p$-goup
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A general diastereoselective synthesis of highly functionalized ferrocenyl ambiphiles enabled on a large scale by electrochemical purification

2017

International audience; A general synthesis of highly functionalized ferrocenes, which include (P,B)- and (N,B)-ambiphiles, has been developed at a multigram scale. Diastereoselective stepwise modification of di-tert-butylated ferrocenes included the unprecedented separation of electroactive species. Bulky alkyl groups on ferrocenes ensure planar chirality of ambiphiles and enforce closer proximity of antagonist Lewis functions.

catalytic applicationsPlanar chirality010402 general chemistryElectrochemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesCatalysisMaterials ChemistryOrganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryfree hydrogen activationaryl bromidesAlkylchemistry.chemical_classificationcomplexes010405 organic chemistryChemistryligandsdirect arylationMetals and AlloysGeneral ChemistrypalladiumCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsfrustrated lewis pairsCeramics and Compositescoordination chemistry
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Comparative studies of oxidation processes on Group 10 Metals Dithiolene Derivatives in the formation of coordination polymers

2018

This document is the Accepted Manuscript Version of a Published Work that appeared in final form in "Crystal Growth and Design", copyright © 2018 American Chemical Society after peer review and techical editing by publisher. To access the final and published work see "Comparative Studies of Oxidation Processes on Group 10 Metals Dithiolene Derivatives in the Formation of Coordination Polymers Oscar Castillo, Esther Delgado, Carlos J. Gómez-García, Diego Hernández, Elisa Hernández, Pilar Herrasti, Avelino Martín, and Félix Zamora Crystal Growth & Design 2018 18 (4), 2486-2494

chemistry.chemical_classification010405 organic chemistryDianionic tetranickel dithiolene clusterFísicaGeneral ChemistryPolymerQuímica010402 general chemistryCondensed Matter Physics01 natural sciencesMedicinal chemistryRedoxGroup 10 metal dithiolene Ion-Pairs0104 chemical sciencesCoordination polymerschemistryGroup (periodic table)General Materials ScienceGroup 10 metal dithiolene compounds
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The first structurally characterized cationic lanthanide–alkyl complexesElectronic supplementary information (ESI) available: experimental and spectr…

2002

Reaction of rare earth metal–alkyl complexes [Ln(CH2SiMe3)3(THF)2] (Ln = Y, Lu) with B(C6X5)3 (X = H, F) in the presence of crown ethers gives crystallographically characterized ion pairs [Ln(CH2SiMe3)2(CE)(THF)n]+[B(CH2SiMe3)(C6X5)3]– (CE = [12]-crown-4, n = 1; CE = [15]-crown-5 and [18]-crown-6, n = 0).

chemistry.chemical_classificationLanthanideStereochemistryRare earthMetals and AlloysCationic polymerizationGeneral ChemistryIon pairsMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMaterials ChemistryCeramics and CompositesAlkylChemical Communications
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B-DNA Structure and Stability as Function of Nucleic Acid Composition. Dispersion-Corrected DFT Study of Dinucleoside-Monophosphate Single and Double…

2013

actions of the sugar-phosphate skeleton with water; (6) hydrophobic interactions of the DNA cylindrical core, made up by the hydrogen-bonded and stacked nitrogen bases, with the water solvent. Recently, there has been increasing effort in developing and applying quantum chemical methods able to reproduce the structure of native B-DNA and to correctly describe the energy involved in the intrastrand and interstrand noncovalent interactions between the nucleotide monomers. This topic has been approached by both wave function methods and density functional theory. [2] Water solvent and sodium counterions also play an important role in the formation and relative stabilization of the double-helic…

chemistry.chemical_classificationStereochemistryChemistryBase pairHydrogen bondStackingGeneral ChemistryCrystal structureFull Papersstacking interactionsNucleobaseHydrophobic effectCrystallographyDNA structuresSettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationshydrogen bondsNon-covalent interactionsDNA DFT calculations structure stabilityDensity functional theoryWatson–Crick base pairsTheoretical ChemistryGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)
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Rate constants for ion-pair dissociation and association in the anionic two-state polymerization of styrene in THF

1965

chemistry.chemical_compoundReaction rate constantPolymerizationchemistryPolymer chemistryGeneral EngineeringIon pairsDissociation (chemistry)StyreneJournal of Polymer Science Part B: Polymer Letters
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Nickel as a Lewis Base in a T‐Shaped Nickel(0) Germylene Complex Incorporating a Flexible Bis(NHC) Ligand

2018

Flexible, chelating bis(NHC) ligand 2, able to accommodate both cis- and trans-coordination modes, was used to synthesize (2)Ni(η 2 -cod), 3. In reaction with GeCl2, this produced (2)NiGeCl2, 4, featuring a T-shaped Ni(0) and a pyramidal Ge center. Complex 4 could also be prepared from [(2)GeCl]Cl, 5, and Ni(cod)2, in a reaction that formally involved Ni-Ge transmetalation, followed by coordination of the extruded GeCl2 moiety to Ni. A computational analysis showed that 4 possesses considerable multiconfigurational character and the Ni→Ge bond is formed through σ-donation from the Ni 4s, 4p, and 3d orbitals to Ge. (NHC)2Ni(cod) complexes 9 and 10, as well as (NHC)2GeCl2 derivative 11, incor…

chemistry.chemical_elementBite angleorganometalliyhdisteet010402 general chemistry01 natural sciencesCatalysisTransmetalationchemistry.chemical_compoundnickelPolymer chemistryMoietyChelationLewis acids and basesN-heterocyclic carbenesta116010405 organic chemistryLigandGeneral MedicineGeneral Chemistrykompleksiyhdisteet0104 chemical sciencesT-geometryNickelgermaniummetal-only Lewis pairschemistrynikkeliDerivative (chemistry)Angewandte Chemie International Edition
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