0000000000909193

AUTHOR

Raphaël Tripier

showing 5 related works from this author

Electrochemically-driven conformational shift in mono- and di-copper constrained macrotricyclic cyclen receptors

2008

International audience; An electrochemical study of mono- and di-copper constrained cyclen macrotricycles is presented. Electrochemical data in DMF solution indicate that the reduction of dinuclear complexes occurs in two steps in the -0.4 to -0.8 V vs.AgCl/Ag potential range yielding CuII CuI and CuI CuI species further reduced to Cu metal at highly negative potentials. Mononuclear complexes are reduced in two steps to CuI and Cu metal. Electrochemical data suggest that reduction of both mononuclear and dinuclear complexes approach a square scheme involving electrochemically-driven conformational shifts for metal ions. The presence of endo- and exo-forms of the complexes are revealed by ch…

010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryMetal ions in aqueous solutionchemistry.chemical_elementTetraethylammonium chloride010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryCyclen[CHIM.ANAL]Chemical Sciences/Analytical chemistryvisual_artvisual_art.visual_art_medium[CHIM]Chemical SciencesReceptorOctane
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Macrocycle-Based Spin-Crossover Materials

2009

International audience; New iron(II) complexes of formula [Fe(L1)](BF(4))(2) (1) and [Fe(L2)](BF(4))(2) x H(2)O (2) (L1 = 1,7-bis(2'-pyridylmethyl)-1,4,7,10-tetraazacyclododecane; L2 = 1,8-bis(2'-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane) have been synthesized and characterized by infrared spectroscopy, variable-temperature single-crystal X-ray diffraction, and variable-temperature magnetic susceptibility measurements. The crystal structure determinations of 1 and 2 reveal in both cases discrete iron(II) monomeric structures in which the two functionalized tetraazamacrocycles (L1 and L2) act as hexadentate ligands; the iron(II) ions are coordinated with six nitrogen atoms: four from …

Coordination sphere010405 organic chemistryChemistryCrystal structure[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistryTrigonal prismatic molecular geometry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographyParamagnetismMolecular geometrySpin crossoverOctahedral molecular geometry[CHIM]Chemical SciencesPhysical and Theoretical Chemistry
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Reaction of polyamines with diethyloxalate: a convenient route for the synthesis of tetraazacycloalkanes

2006

International audience; The reactivity of various polyamines with diethyloxalate has been investigated. It appears that, in similar experimental conditions, primary diamines give predominantly [2+2] adducts while the use of secondary benzylated polyamines results in [1+1] condensation. Although the intermediate tetraamides formed in the first case are extremely poorly soluble and show very slow reactivity towards reducing agents, cyclam has been obtained by using ultrasounds during the reaction of the corresponding tetraoxomacrocycle with BH 3 /THF. The [1+1] cyclization reaction of diversely N-benzylated linear tetraamines, whose selective syntheses have been devised herein, gives access t…

synthesisReducing agent010402 general chemistry01 natural sciencesAdductlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistry[PHYS.COND.CM-GEN] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other][ CHIM.ORGA ] Chemical Sciences/Organic chemistryAmideCyclamOrganic chemistryReactivity (chemistry)ComputingMilieux_MISCELLANEOUSPrimary (chemistry)010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistrytetraaminesOrganic ChemistryCombinatorial chemistry0104 chemical sciences[PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]AminalAmine gas treating
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Polyamines and applications. A look at the first workshop in linear and cyclic polyamines chemistry

2008

Given their versatile coordination properties, cyclic and linear polyamines are the subject of numerous worksin many research groups. This great interest is mainly related to their use in diverse fields such as removalof metals from liquids, purification of gases, application in catalysis, in sensors, as well as in various probesfor medical applications. This paper summarizes recent results obtained by the French research groupswhich attended the first ìworkshop in linear and cyclic polyamines chemistryî.

[CHIM.INOR] Chemical Sciences/Inorganic chemistryPolyamines cycliquescoordinationco ordinationextraction/puri fication[CHIM.INOR]Chemical Sciences/Inorganic chemistrycatalysehybrid materials.[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCyclic polyaminesluminescence[CHIM.COOR]Chemical Sciences/Coordination chemistrylinear polyaminescomplexesvectorisationcatalysisextraction/Èpur ation[CHIM.ORGA]Chemical Sciences/Organic chemistrymatÈriaux hybrides[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistryIR M[CHIM.ORGA] Chemical Sciences/Organic chemistrypolyamines linÈairesMRI
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Polyamines : études et applications

2008

International audience

complexescoordinationvectorisationextraction/purificationcatalysis[CHIM.ORGA]Chemical Sciences/Organic chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistrycyclic polyamines[ CHIM.ORGA ] Chemical Sciences/Organic chemistryhybrid materialsluminescenceComputingMilieux_MISCELLANEOUSlinear polyaminesMRI
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