Search results for "complexe"

showing 10 items of 920 documents

Cyclotriveratrylene-Containing Porphyrins

2016

International audience; The C-3-symmetric cyclotriveratrylene (CTV) was covalently bonded via click chemistry to 1, 2, 3, and 6 zinc(II) porphyrin units to various host for C-60. The binding constants, Ka, were measured from the quenching of the porphyrin fluorescence by C-60. These constants vary between 400 and 4000 M-1 and are considered weak. Computer modeling demonstrated that the zinc(II) porphyrin units, [Zn], exhibit a strong tendency to occupy the CTV cavity, hence blocking the access for C-60 to land on this site. Instead, the pincer of the type [Zn]-[Zn] and in one case [Zn]-CTV, were found to be the most probable geometry to promote host-guest associations in these systems.

cagesStereochemistrychemistry.chemical_elementCyclotriveratryleneZinc010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessupramolecular chemistrydendrimersInorganic Chemistrychemistry.chemical_compoundc-60[CHIM]Chemical SciencesmoleculesctvPhysical and Theoretical Chemistryinclusion complexesQuenching (fluorescence)010405 organic chemistryfullereneFluorescencePorphyrin0104 chemical sciencesPincer movementCrystallographychemistryCovalent bondClick chemistryderivativeshosts
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Badanie właściwości inkluzyjnych p-tert-butylokaliksarenów metodą inwersyjnej chromatografii gazowej

2007

Metodą QSRR scharakteryzowano właściwości inkluzyjne p-tert-butylokaliksarenów o 4, 6 i 8 merach w cyklu oraz ich octanów, wykorzystując do tego celu inwersyjną chromatografię gazową. W badaniach zastosowano przy tym dwa szeregi homologiczne solutów - alkohole alifatyczne oraz benzen i jego homologi. Stwierdzono, że zdolności inkluzyjne w znacznym stopniu zależą od wymiarów luki molekularnej cyklomeru. Zamiana w kaliksarenach grup wodorotlenowych na octanowe nie wywiera natomiast istotnego wpływu na możliwości tworzenia kompleksów typu gość-gospodarz. Wyniki uzyskane metodą QSRR potwierdzono wyznaczonymi wartościami indeksów Kovátsa.

calixareneskaliksarenyinverse gas chromatographykompleksy inkluzyjneinclusion complexesinwersyjna chromatografia gazowaPolimery
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Badanie metodą inwersyjnej chromatografii gazowej wpływu wielkości podstawnika na właściwości inkluzyjne kaliksarenów

2009

Badano wpływ wielkości alifatycznego podstawnika na zdolności inkluzyjne kaliksarenów {kaliks[4]arenu(K4), p-izopropylokaliks[4]arenu (IPK4) i p-tert-butylokaliks[4]arenu (TBK4)}. Oceny wpływu dokonywano za pomocą metody QSRR przy użyciu inwersyjnej chromatografii gazowej. W charakterze solutów użyto szeregu alifatycznych alkoholi, homologów benzenu i homologów pirydyny. Na podstawie indeksów retencji Kovatsa i wykresów zależności właściwej objętości retencji od temperatury wrzenia [Vg=f(Tw)] stwierdzono, że tylko podstawione kaliksareny wykazują właściwości inkluzyjne w stosunku do niższych alkoholi.

calixareneskaliksarenyinverse gas chromatographykompleksy inkluzyjnewłaściwa objętość retencjispecific retention volumeinclusion complexesinwersyjna chromatografia gazowaPolimery
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Influence of Anion and Cation Structure of Ionic Liquids on Carboxylic Acids Extraction

2019

A recently proposed new mechanism and a model of reactive extraction of carboxylic acids by hydrophobic ionic liquids (ILs) was tested on five systems from published as well as from new equilibrium data on liquid-liquid extraction of butyric and lactic acids (BA and LA) from aqueous solutions. Two phosphonium and one ammonium ILs were used. The model describes experimental data for all systems with a good fit. The mechanism of acid extraction by ILs is very similar for all tested systems. This indicates a more general validity of the developed model. The model allows deeper understanding of regularities in carboxylic acid extraction by hydrophobic ILs. Stability constants of the first acid-…

carboxylic acidsL/L equilibriumCarboxylic acid02 engineering and technologyPhosphinate010402 general chemistry01 natural sciencesHydrophobic effectlcsh:Chemistryionic liquidschemistry.chemical_compoundPolymer chemistryPhosphoniumOriginal Researchchemistry.chemical_classificationAqueous solutionmodelGeneral Chemistry021001 nanoscience & nanotechnologyinfluence of structure0104 chemical sciencesSolventChemistrychemistrylcsh:QD1-999Stability constants of complexesIonic liquidextraction0210 nano-technologyFrontiers in Chemistry
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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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Analyser les catastrophes : une approche par les comportements humains

2011

La catastrophe est une forme de crise qui altère profondément un système social soumis à une situation de stress collectif. Ce dernier est confronté à une agression qui surpasse ses capacités d'adaptation induisant une désorganisation sociale et territoriale plus ou moins longue. L'environnement physique, qui influe peu sur les comportements observés en situation normale, contrairement à l'environnement social, impose de nouvelles façons d'agir, de nouveaux modes d'organisation, quelles que soient les échelles considérées. Il s'agit au moment du choc d'assurer sa survie et celle de ses proches (à condition qu'ils ne soient pas trop éloignés spatialement), puis une fois le danger écarté, de …

catastrophe[SHS.GEO] Humanities and Social Sciences/Geography[SHS.GEO]Humanities and Social Sciences/Geographysystèmes complexesémergencecomportement humaintypologie[ SHS.GEO ] Humanities and Social Sciences/Geography
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Coordination chemistry on surfaces through vapor phase processing: smart molecular/graphene heterostructures based on spin-crossover complexes and 2D…

2023

Los compuestos de coordinación están últimamente focalizando la atención de los investigadores en el campo de la nanociencia. Particular interés están generando aquellos compuestos con propiedades magnéticas de cara a su integración a la nanoescala en ramas como la electrónica y/o la espintrónica moleculares. Sin embargo, para su uso real en dispositivos destinados a estas aplicaciones, su procesabilidad es un requisito indispensable. En el marco de esta necesidad, la presente tesis doctoral se ha destinado al estudio del procesado sobre superficies mediante técnicas de fase gas de dos tipos distintos de compuestos de coordinación. Por tanto, el trabajo se ha dividido en dos partes. La prim…

chemistry on surfacesspin-crossoverUNESCO::QUÍMICAsublimable moleculesmolecular magnetismcoordination complexessmart heterostructurestwo-dimensional materialslayered coordination polymerschemical vapor deposition
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A nucleophilic gold complex.

2019

Solid-state auride salts featuring the negatively charged Au– ion are known to be stable in the presence of alkali metal counterions. While such electron-rich species might be expected to be nucleophilic (in the same manner as I–, for example), their instability in solution means that this has not been verified experimentally. Here we report a two-coordinate gold complex (NON)AlAuPtBu3 (where NON is the chelating tridentate ligand 4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethylxanthene) that features a strongly polarized bond, Auδ––Alδ+. This is synthesized by reaction of the potassium aluminyl compound [K{Al(NON)}]2 with tBu3PAuI. Computational studies of the complex, includ…

chemistry.chemical_classification010405 organic chemistryChemistryLigandGeneral Chemical EngineeringAtoms in moleculesGeneral Chemistrykompleksiyhdisteetgold010402 general chemistryAlkali metal01 natural scienceskulta0104 chemical sciencesIonElectronegativityCrystallographyNucleophileCovalent bondcoordination complexesCounterionNature chemistry
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Anticancer study of heterobimetallic platinum(II)-ruthenium(II) and platinum(II)-rhodium(III) complexes with bridging dithiooxamide ligand

2019

Abstract Three heterobimetallic platinum (II)/ruthenium (II) and platinum (II)/rhodium (III) complexes, A: Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}-[Ru (p-cymene)Cl], R = isoamyl; B: Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}[Rh (phpy)2], R = isoamyl; C: [Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}-[Rh(C5Me5)Cl]], R = benzyl, were prepared from mononuclear complexes 1 and 2, 1: [Pt (H-isoamyl2DTO)2]; 2: [Pt (H-benzyl2DTO)2], DTO = dithiooxamide, by reaction of 1 or 2 with the corresponding chlorido-bridged dimers, [Rh(C5Me5)Cl (μ-Cl)]2, [Ru (p-cymene)Cl (μ-Cl)]2 or [Rh (phpy)2 (μ-Cl)]2, and then evaluated as anticancer agents for the inhibition of the three proteolytic activities of human 20S proteasome, one of the main target …

chemistry.chemical_classification010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_element010402 general chemistrymedicine.disease01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesRhodiumRutheniumAnticancer; Dithiooxamide; Heterobimetallic; Platinum complexes; Rhodium; RutheniumInorganic Chemistrychemistry.chemical_compoundEnzymeDithiooxamideApoptosisNeuroblastomaMaterials ChemistrymedicinePhysical and Theoretical ChemistryPlatinumCytotoxicityJournal of Organometallic Chemistry
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Influence of structural elements on iron(III) chelating properties in a new series of amino acid-derived monohydroxamates

2018

Abstract A series of amino acid-derived monohydroxamate compounds A1 – A7 was synthesized and characterized for their coordination properties of Fe(III). The series varies in their skeletal lengths and compositions; some compounds lack external substituents, others are substituted with external functional amino or carboxylic groups, or alternatively inert methyl. Undertaken investigations allowed the determination of stoichiometry, stability constants and spectroscopic parameters of formed ferric complexes. Incorporation of an external functional group with a dissociable proton affects the coordination behavior; the presence of carboxylic or amino groups hampers the formation of mono-, di- …

chemistry.chemical_classification010405 organic chemistryChemistryStereochemistrySiderophores010402 general chemistry01 natural sciences0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundHydroxamatesFe(III) complexesFunctional groupPolymer chemistryMaterials ChemistrymedicineFerricChelationPhysical and Theoretical ChemistryStoichiometrymedicine.drugInorganica Chimica Acta
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