Ligands, Complex Architectures and Catalysis (Team G)

LCC

Overview

Since its creation, the “Ligands, Complex Architectures and Catalysis” team has gathered a wide range of expertise in organic chemistry and heterochemistry of ligands, coordination chemistry, organometallic chemistry, homogeneous catalysis, studies of reaction mechanisms by experimental methods (including kinetics) and theoretical methods, and atom transfer radical polymerization.

Members of the team

All
Directeur de recherche

MANOURY Eric

Professeur

DEYDIER Eric

Doctorante

ABOU FAYSSAL Chantal

Senior Associate Professor + Habilitation

AGUSTIN Dominique

Master 2

AMBERT Dorian

AUDIN Catherine
Maître de conférences

AUDIN Catherine

BACQUE Cecilia
Etudiante

BACQUE Cecilia

Student

BAYSSINE Abdelhakim

BEZVUHLIAK Yuliia
Student

BEZVUHLIAK Yuliia

BIBAL-KOEPKE Christine
Maître de conférences

BIBAL-KOEPKE Christine

Directeur de recherche

DARAN Jean-Claude

Doctorant

FAGUÉ Vincent

Chargé de recherche

FLIEDEL Christophe

FORGET Laurianne
PhD student

FORGET Laurianne

GARG Nidhi
Chercheur invité

GARG Nidhi

Maître de conférences

GUILLO Pascal

Doctorant

HAIDAR Ali Alhadi

Master 2

HARB Jana

Doctorant

KISTEN Paven

Chargée de recherche

LABANDE Agnes

MASSOU Stephane
ITA

MASSOU Stephane

Doctorant

MICHELAS Maxime

Doctorante

MURALI Meenu

MURILLO-GUILLEN Maranda
Student

MURILLO-GUILLEN Maranda

Professeur

POLI Rinaldo

Doctorant

PULIDO DIAZ Israel

Guest

RAZA Arsen

CDD

RUZHYLO Illia

Etudiante

STEPHEN Treesa

ITA

VINCENDEAU Sandrine

Master 2

VOROZHBIAN Anna

Doctorante

YANG Runqian

Guest

ZEROUGH Izid-bih

No Results Found

Directeur de recherche

MANOURY Eric

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Ancien élève de l’ENS CACHAN. Doctorat sous la supervision de Gilbert Balavoine à l’Université Paris-Sud Orsay (Epoxydation asymétrique des alcènes utilisant des borates chiraux), stage postdoctoral avec K. Barry Sharpless au MIT (Dihydroxylation asymétrique des alcènes utilisant des complexes de l’osmium). CR CNRS de 1992 à 2013 à l’Université Paris-Sud Orsay puis au Laboratoire de Chimie de Coordination de Toulouse (LCC). DR au LCC depuis 2013. Directeur Adjoint du LCC depuis 2018.

Email:eric.manoury(at)lcc-toulouse.fr

Téléphone:05.61.33.31.74

Bureau:B213

Equipe:G

Professeur

DEYDIER Eric

Numéro ORCID : 0000-0001-9662-9572

Après un doctorat sur des complexes à ligands diazoalcanes C-coordinés, j’ai effectué un postdoc à CALTECH sur les cinétiques de transfert d’électrons (complexes d’iridium). En tant que MCF à Castres, j’ai travaillé sur la valorisation des cendres de farines animales puis, depuis mon rattachement au LCC en 2007, sur la catalyse asymétrique par des complexes métalliques. Actuellement, je travaille sur l’hétérogénéisation de catalyseurs chiraux pour recyclage et développement de procédés en continu.

Email:eric.deydier(at)lcc-toulouse.fr

Téléphone:05.63.62.11.66

Bureau:Castres

Equipe:G

Doctorante

ABOU FAYSSAL Chantal

Email:chantal.aboufayssal(at)lcc-toulouse.fr

Téléphone:0561333174

Bureau:C226

Equipe:G

Senior Associate Professor + Habilitation

AGUSTIN Dominique

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– PhD at LHFA (Toulouse)
– post-doc at Saarland University (Germany)
– MCF (assistant Professor) 2002-2006 at UPMC (Sorbonne University, Paris)
– MCF since 2006 at Paul Sabatier University (IUT, Castres)
– Habilitation in 2012

Numéro ORCID : 0000-0003-1933-8442

– President of the Research Commission of the IUT Castres
– Secretary of Sustainable Chemistry Division of the French Chemical Society
– Co-pilot of Science Popularization Meetings : Exploreur Science en Circuit Court– Castres
– member of LCC – Sustainable Workgroup
– Member of the IUT Paul Sabatier Ecological Transition Steering Committee
– TIRIS Training Programs Steering Committee Facilitator

Email:dominique.agustin(at)lcc-toulouse.fr

Telephone:05.63.62.11.72

Room:Castres

Team:G

Master 2

AMBERT Dorian

Email:dorian.ambert(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C224

Equipe:G

Maître de conférences

AUDIN Catherine

Email:catherine.audin(at)lcc-toulouse.fr

Téléphone:05.63.62.11.54

Bureau:CASTRES

Equipe:G

Etudiante

BACQUE Cecilia

Email:cecilia.bacque(at)lcc-toulouse.fr

Téléphone:05.61.33.31.58

Bureau:C226

Equipe:G

Student

BAYSSINE Abdelhakim

Email:abdelhakim.bayssine(at)lcc-toulouse.fr

Phone:05.63.62.11.72

Office:CASTRES

Team:G

Student

BEZVUHLIAK Yuliia

Email:yuliia.bezvuhliak(at)lcc-toulouse.fr

Phone:05.61.33.31.74

Office:C222

Team:G

Maître de conférences

BIBAL-KOEPKE Christine

Email:christine.bibal-koepke(at)lcc-toulouse.fr

Téléphone:05.63.62.11.55

Bureau:Castres

Equipe:G

Directeur de recherche

DARAN Jean-Claude

Email:jean-claude.daran(at)lcc-toulouse.fr

Téléphone:05.61.33.31.74

Bureau:B225

Equipe:G

Doctorant

FAGUÉ Vincent

Email:vincent.fague(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C224

Equipe:G

Chargé de recherche

FLIEDEL Christophe

Numéro ORCID : 0000-0003-1442-0682

Christophe Fliedel a obtenu son doctorat de l’Université de Strasbourg (France) en 2010, sous la direction du Dr Pierre Braunstein. Il a ensuite effectué un stage postdoctoral à l’Université Nouvelle de Lisbonne (Portugal). En 2016, il a été recruté par le CNRS en tant que chargé de recherche et a intégré le Laboratoire de Chimie de Coordination à Toulouse. Ses activités de recherche se concentrent sur la chimie de coordination, la chimie organométallique et les réactions de polymérisation.

Email:christophe.fliedel(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C224

Equipe:G

PhD student

FORGET Laurianne

Email:laurianne.forget(at)lcc-toulouse.fr

Phone:05.61.33.31.66

Office:C226

Team:G

Chercheur invité

GARG Nidhi

Email:nidhi.garg(at)lcc-toulouse.fr

Téléphone:05.61.33.31.73

Bureau:B211

Equipe:G

Maître de conférences

GUILLO Pascal

Numéro ORCID : 0000-0002-9818-7824

Après un doctorat axé sur les complexes métalliques dinucléaires pour des applications photocatalytiques, j’ai développé pendant mon postdoc des catalyseurs hétérogènes Ta-Ge pour l’époxydation et leurs analogues moléculaires. Actuellement, je conçois des catalyseurs avec différents objectifs et plusieurs approches : influence de la seconde sphère de coordination en catalyse, hétérogénéisation des catalyseurs moléculaires, réactions de couplage C-C basées sur de nouveaux processus d’activation.

Email:pascal.guillo(at)lcc-toulouse.fr

Téléphone:05.63.62.11.61

Bureau:Castres

Equipe:G

Doctorant

HAIDAR Ali Alhadi

Email:alialhadi.haidar(at)lcc-toulouse.fr

Téléphone:06.23.90.73.23

Bureau:Castres

Equipe:G

Master 2

HARB Jana

Email:jana.harb(at)lcc-toulouse.fr

Téléphone:05.61.33.31.38

bureau:B106

Equipes:G et V

Doctorant

KISTEN Paven

Domaines d’expertise : Spectroscopie RMN, synthèse de ligands et catalyse

Paven est doctorant sous la direction conjointe de Simon Duckett, Jason Lynam et John Slattery à York et de Rinaldo Poli à Toulouse. Dans le cadre du réseau ITN CCIMC, le projet vise à mieux comprendre les mécanismes de catalyse impliqués dans les processus d’hydrogénation asymétrique et d’hydrogénation par transfert. A York, les espèces organométalliques transitoires présentes dans ces cycles catalytiques seront étudiées à l’aide de la RMN, complétée par des études théoriques utilisant la DFT.

Doctorat en cotutelle entre l’Université de York et le Laboratoire de Chimie de Coordination du CNRS.
Dans le cadre de l’ITN CCIMC, ce projet a reçu un financement du programme de recherche et d’innovation Horizon 2020 de l’Union européenne (convention Marie Skłodowska-Curie n° 860322).

Email:paven.kisten(at)lcc-toulouse.fr

Téléphone:05.61.33.31.85

Bureau:B217

Equipe:G

Chargée de recherche

LABANDE Agnes

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Après une thèse sur les nanoparticules d’or fonctionnalisées comme sondes redox en 2000, sous la direction du Prof. Didier Astruc (Bordeaux), Agnès Labande a effectué un postdoctorat à l’Université d’Oxford (Angleterre) de 2001 à 2003, chez le Prof. David M. Hodgson. Depuis octobre 2003, elle est Chargée de Recherche CNRS au LCC, où elle développe de nouveaux ligands NHCs et ferrocéniques pour la catalyse.

Email:agnes.labande(at)lcc-toulouse.fr

Téléphone:05.61.33.31.58

Bureau:B214

Equipe:G

ITA

MASSOU Stephane

Email:stephane.massou(at)lcc-toulouse.fr

Téléphone:05.61.33.31.96

Bureau:B036

Equipe:G, O et P

Doctorant

MICHELAS Maxime

Après un Master de Chimie des Polymères pour Technologies Avancées (Grenoble), j’ai effectué un stage chez le Prof. Sébastien Perrier à Warwick (Angleterre). Suite à cela, j’ai débuté mon doctorat au LCC sous la supervision du Prof. Rinaldo Poli et du Dr. Christophe Fliedel (ANR-POLYSWTICH). L’objectif de ce projet, qui allie chimie des polymères et de coordination, est de concevoir de nouveaux modérateurs à base de cobalt pour la polymérisation contrôlée par voie radicalaire et ouverture de cycle.

Email:maxime.michelas(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C224

Equipe:G

Doctorante

MURALI Meenu

Email:meenu.murali(at)lcc-toulouse.fr

Téléphone:05.61.33.31.85

Bureau:B217

Equipe:G

Student

MURILLO-GUILLEN Maranda

Email:maranda.murillo-guillen(at)lcc-toulouse.fr

Phone:05.63.62.11.72

Office:CASTRES

Team:G

Professeur

POLI Rinaldo

Numéro ORCID : 0000-0001-9662-9572

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Email:rinaldo.poli(at)lcc-toulouse.fr

Téléphone:05.61.33.31.73

Bureau:B225

Equipe:G

Doctorant

PULIDO DIAZ Israel

Email:Israel.Pulido-Diaz(at)lcc-toulouse.fr

Téléphone:05.63.62.11.72

Bureau:Castres

Equipe:G

Guest

RAZA Arsen

Email:arsen.raza(at)lcc-toulouse.fr

Phone:05.61.33.31.66

Office:C226

Team:G

CDD

RUZHYLO Illia

Numéro ORCID : 0000-0002-7565-5840

Je m’appelle Ruzhylo Illia et je viens d’Ukraine, où j’ai obtenu ma licence en chimie à l’Université nationale Taras Shevchenko de Kiev en 2018. Ensuite, j’ai reçu une bourse du gouvernement français, qui m’a permis d’étudier à l’Université Paul Sabatier et d’obtenir mon master chimie verte en 2019. Actuellement, je suis doctorant et je travaille sous la supervision du Dr Agnès Labande sur l’application de complexes de dirhodium contenant des ligands ferrocéniques en catalyse.

Email:illia.ruzhylo(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C226

Equipe:G

Etudiante

STEPHEN Treesa

Email:treesa.stephen(at)lcc-toulouse.fr

Téléphone:05.63.62.11.72

Bureau:CASTRES

Equipe:G

ITA

VINCENDEAU Sandrine

Email:sandrine.vincendeau(at)lcc-toulouse.fr

Téléphone:05.61.33.31.58

Bureau:B214

Equipe:G

Master 2

VOROZHBIAN Anna

Email:anna.vorozhbian(at)lcc-toulouse.fr

Téléphone:05.61.33.31.58

Bureau:C226

Equipe:G

Doctorante

YANG Runqian

Email:Runqian.Yang(at)lcc-toulouse.fr

Téléphone:05.61.33.31.66

Bureau:C226

Equipe:G

Guest

ZEROUGH Izid-bih

Email:izid-bih.zerough(at)lcc-toulouse.fr

Phone:05.61.33.31.66

Office:C224

Team:G

Research topics

Ligands and complexes

Complex architectures

Catalysis

Team news

Chemistry goes green.

Chemistry goes green.

Listen to the podcast “Les Deux Font La Paire”
recorded on the occasion of the Researchers’ Night 2022.

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Publications

2024

Rh nanoparticles confined in triphenylphosphine oxide-functionalized core-crosslinked micelles with a polyanionic shell: Synthesis, characterization, and application in aqueous biphasic hydrogenation
Abou-Fayssal C. J., Schill L., Poli R., Riisager A., Manoury E., Philippot K.
Reactive and Functional Polymers 2024, 205, 106061/1-8.
https://doi.org/10.1016/j.reactfunctpolym.2024.106061
https://hal.science/hal-04725286

[Rh2(phesp)2]: a bulkier [Rh2(esp)2] analog to tune the site-selectivity in carbene C–H insertion reactions
Labande A., Ruzhylo I., Vorozhbian A., Vincendeau S., Saget T., Mallet-Ladeira S., Dauban P., Manoury E.
ChemCatChem, 2024, e202400874/1-12.
https://doi.org/10.1002/cctc.202400874
https://hal.science/hal-04574738

Benchtop-stable carbyl iminopyridyl NiII complexes for olefin polymerization
Rauf H. S., Liu Y.-S., Arslan M., Solanki S. P. S., Deydier E., Poli R., Grabow L. C., Harth E.
ACS Catalysis 2024, 14(17), 13136-13147.
https://doi.org/10.1021/acscatal.4c02708
https://hal.science/hal-04692509

Synthesis and characterization of new highly fluorinated phosphoramidates bearing different alkylamino groups
Argoubi S., Sanhoury M. A., Zerough I., Manoury E., Chehidi I.
Synthetic Communications 2024, 54(15), 1273-1283.
https://doi.org/10.1080/00397911.2024.2382784
https://hal.science/hal-04665277

Polymeric nanoreactors for catalytic applications
Abou-Fayssal C. J., Poli R., Philippot K., Riisager A., Manoury E.
Comptes Rendus Chimie 2024, 27(S1), 1-23.
https://doi.org/10.5802/crchim.301
https://hal.science/hal-04635254

Impact of POM’s coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts
Pisk J., Vrdoljak V., Mandarić M., Hrenar T., Agustin D., Rubčić M.
RSC Advances 2024, 14(27), 19029-19040.
http://dx.doi.org/10.1039/D4RA03563A
https://hal.science/hal-04632363

Molybdenum complexes derived from 2-hydroxy-5-nitrobenzaldehyde and benzhydrazide as potential oxidation catalysts and semiconductors
Pisk J., Šušković M., Topić E., Agustin D., Judaš N., Pavić L.
International Journal of Molecular Sciences 2024, 25(9), 4859/1-16.
https://doi.org/10.3390/ijms25094859
https://hal.science/hal-04593900

Coordination Chemistry Inspires Molecular Catalysis
Poli R., Caminade A.-M. (Eds).
Zenodo, 2024.
https://doi.org/10.5281/zenodo.10966127
https://hal.science/hal-04548441

One-pot synthesis of Rh nanoparticles in polycationic-shell, triphenylphosphine oxide-functionalized core-crosslinked micelles for aqueous biphasic hydrogenation
Abou-Fayssal C. J., Schill L., Poli R., Manoury E., Philippot K., Riisager A.
ChemCatChem 2024, 16(15), e202400189/1-10.
https://doi.org/10.1002/cctc.202400189
https://hal.science/hal-04524464

Mechanistic insights of the Ir-bipyridonate catalyzed aqueous methanol dehydrogenation and transfer dehydrogenation to acetophenone: Experimental and DFT study
Garg N., Poli R., Sundararaju B.
European Journal of Inorganic Chemistry 2024, 27(13), e202300744/1-10.
https://doi.org/10.1002/ejic.202300744
https://hal.science/hal-04502966

Preparative and catalytic properties of MoVI mononuclear and metallosupramolecular coordination assemblies bearing hydrazonato ligands
Mandarić M., Topić E., Agustin D., Pisk J., Vrdoljak V.
International Journal of Molecular Sciences 2024, 25 (3), 1503/1-17.
https://doi.org/10.3390/ijms25031503
https://hal.science/hal-04501274

Peculiar catalytic properties of oxide glass-(ceramics) in epoxidation reactions
Pisk J., Marijan S., Klaser T., Mošner P., Koudelka L., Agustin D., Skoko Ž., Pavić L.
Journal of Non-Crystalline Solids 2024, 626, 122780/1-5.
https://doi.org/10.1016/j.jnoncrysol.2023.122780
https://hal.science/hal-04503149

Hafnium coordination vitrimer based on carboxylate exchange: synthesis, properties, and mechanistic investigations on the [Hf6O4(OH)4(O2CMe)12]2 model compound
Murali M., Berne D., Daran J.-C., Bijani C., Manoury E., Leclerc E., Caillol S., ladmiral V., Joly-Duhamel C., Poli R.
European Journal of Inorganic Chemistry 2024, 27(8), e202300672.
https://doi.org/10.1002/ejic.202300672
https://hal.science/hal-04427867

New protocol for the synthesis of S-thioesters from benzylic, allylic and tertiary alcohols with thioacetic acid
Lachguar A., Bandyopadhyay U., Ech-Chariy M., Vincendeau S., Audin C., Daran J.-C., Manoury E., Poli R., Deydier E.
Chemistry – A European Journal 2024, 30(1), e202302551/1-13.
https://doi.org/10.1002/chem.202302551
https://hal.science/hal-04268374

2023

Improving the kinetic resolution of rac-2-(diphenylthiophosphinoferrocene) methanol catalyzed by Thermomyces lanuginosus lipase immobilized on immobead-150
Santana Fróes N. O., Bandyopadhyay U., Negreiro J. M., de Sousa Fonseca T., Nunes F. M., de Mattos M. C., Zanatta G., de Melo Pereira J. V., de Jesus Guimarães C., do Ó Pessoa C., Poti e Silva B., Manoury E., Ferreira Oliveira M. C.
Molecular Catalysis 2023, 535, 112867/1-9.
https://doi.org/10.1016/j.mcat.2022.112867
https://hal.science/hal-04669292

Coordination adaptable networks: Introducing vitrimer properties using dynamic coordination bonds
Murali M., Manoury E., Poli R.
European Journal of Inorganic Chemistry 2023, 26(36), e202300574/1-13.
https://doi.org/10.1002/ejic.202300574
https://hal.science/hal-04269901

Combination of fluorine and tertiary amine activation in catalyst-free thia-michael covalent adaptable networks
Berne D., Poli R., Caillol S., Ladmiral V., Leclerc E.
Macromolecules 2023, 56(20), 8260–8274.
https://doi.org/10.1021/acs.macromol.3c01129
https://hal.science/hal-04232888

Hydrogenation and dehydrogenation of N-heterocycles under Cp*Co(III)-catalysis
Dahiya P., Garg N., Poli R., Sundararaju B.
Dalton Transactions 2023, 52(41), 14752-14756.
http://dx.doi.org/10.1039/D3DT03161F
https://hal.science/hal-04232849

Role of organic solvent and influence of oxidant in the oxidation of linalool catalyzed by molybdenum and vanadium complexes
Haidar A. A. H., Agustin D.
Tetrahedron Green Chem 2023, 2, 100029/1-8.
https://doi.org/10.1016/j.tgchem.2023.100029
https://hal.science/hal-04233003

Confinement of Rh nanoparticles in triphenylphosphine oxide-functionalized core-crosslinked micelles for aqueous biphasic hydrogenation catalysis
Abou-Fayssal C. J., Fliedel C., Poli R., Riisager A., Philippot K., Manoury E.
Materials Today Chemistry 2023, 34, 101752/1-10.
https://doi.org/10.1016/j.mtchem.2023.101752
https://hal.science/hal-04232955

Asymmetric syntheses of enantioenriched 2,5-disubstituted pyrrolidines
Lazib Y., Naves J. G., Labande A., Dauban P., Saget T.
ACS Organic & Inorganic Au 2023, 3(3), 120-129.
https://doi.org/10.1021/acsorginorgau.2c00061
https://hal.science/hal-04210008

Acetate ion addition to and exchange in (1,5-cyclooctadiene)rhodium(i) acetate: relevance for the coagulation of carboxylic acid-functionalized shells of core-crosslinked micelle latexes
Fiore A. M., Petrelli V., Fliedel C., Manoury E., Mastrorilli P., Poli R.
Dalton Transactions 2023, 52(35), 12534-12542.
http://dx.doi.org/10.1039/D3DT02260A
https://hal.science/hal-04194797

Homolytic PdII–C bond cleavage in the MILRad process: Reversibility and termination mechanism
Poli R., Nguyen D. H., Liu Y.-S., Harth E.
Organometallics 2023, 42(16), 2277-2286.
https://doi.org/10.1021/acs.organomet.3c00277
https://hal.science/hal-04194769

Termination of the carbomethoxyisopropyl radical, a poly(methyl methacrylate) model, in the presence of copper complexes and proton donors
Sobieski J., Silab S. D., Thevenin L., Matyjaszewski K., Fliedel C., Poli R.
Macromolecules 2023, 56(16), 6339-6353.
https://doi.org/10.1021/acs.macromol.3c00545
https://hal.science/hal-04194741

Acetate exchange mechanism on a Zr12 oxo hydroxo cluster: Relevance for reshaping zr-carboxylate coordination adaptable networks
Murali M., Bijani C., Daran J.-C., Manoury E., Poli R.
Chemical Science 2023, 14(30), 8152-8163.
http://dx.doi.org/10.1039/D3SC02204H
https://hal.science/hal-04155107

Transamidation vitrimers enabled by neighbouring fluorine atom activation
Berne D., Tanguy G., Caillol S., Poli R., Ladmiral V., Leclerc E.
Polymer Chemistry 2023, 14(30), 3479-3492.
http://dx.doi.org/10.1039/D3PY00577A
https://hal.science/hal-04174700

Redox-responsive catalysis: fine tuning of chemoselectivity in the intramolecular reaction of diazo compounds catalysed by ferrocene-functionalised dirhodium(ii) complexes
Ruzhylo I., Vincendeau S., Dauban P., Manoury E., Poli R., Labande A.
New Journal of Chemistry 2023, 47(20), 9601-9610.
https://dx.doi.org/10.1039/D3NJ01131C
https://hal.science/hal-04099187

A mononuclear cobalt(III) carboxylate complex with a fully O-based coordination sphere: CoIII-O bond homolysis and controlled radical polymerisation from [Co(acac)2(O2CPh)]
Michelas M., Daran J.-C., Saquet A., Fliedel C., Poli R.
Dalton Transactions 2023, 52(20), 6791-6798.
http://dx.doi.org/10.1039/D3DT00910F
https://hal.science/hal-04084576

Facile assembly of C–N bond-containing polymer electrolytes enabled by lithium salt-catalyzed aza-Michael addition
Wang J., Zhang C., Zhang Y., Chen G., Poli R., Xie X., Xue Z.
Macromolecules 2023, 56(6), 2484-2493.
https://doi.org/10.1021/acs.macromol.2c02230
https://hal.science/hal-04036882

A new classification for the ever-expanding mechanistic landscape of catalyzed hydrogenations, dehydrogenations and transfer hydrogenations
Poli R.
in Advances in Organometallic Chemistry. Pérez Pedro J. (Ed.). Elsevier/Academic Press: Cambridge, 2023, vol. 79, pp. 87-133. (978-0-443-18888-6).
https://doi.org/10.1016/bs.adomc.2022.10.002
https://hal.science/hal-04016457

Cobalt(II) and cobalt(III) complexes of tripodal tetradentate diamino-bis(phenolate) ligands: Synthesis, characterization, crystal structures and evaluation in radical polymerization processes
Michelas M., Redjel Y. K., Daran J.-C., Benslimane M., Poli R., Fliedel C.
Inorganica Chimica Acta 2023, 549, 121408/1-9.
https://doi.org/10.1016/j.ica.2023.121408
https://hal.science/hal-04008189

Catalyst-free thia-Michael addition to alpha-trifluoromethylacrylates for 3D network synthesis
Berne D., Lemouzy S., Guiffrey P., Caillol S., Ladmiral V., Manoury E., Poli R., Leclerc E.
Chemistry – A European Journal 2023, 29(20), e202203712/1-10.
https://doi.org/10.1002/chem.202203712
https://hal.science/hal-03972802

IrI(η4-diene) precatalyst activation by strong bases: formation of an anionic IrIII tetrahydride
Kisten P., Manoury E., Lledos A., Whitwood A. C., Lynam J. M., Slattery J. M., Duckett S. B., Poli R.
Dalton Transactions 2023, 52(8), 2495-2505.
http://dx.doi.org/10.1039/D2DT04036K
https://hal.science/hal-03960179

Synthesis of tris[2-(dimethylamino)ethyl]amine with regiospecific deuterium labels
Sobieski J., Ruzhylo I., Szczepaniak G., Gorczyński A., Matyjaszewski K., Manoury E., Poli R.
ChemistrySelect 2023, 8(5), e202300053/1-5.
https://doi.org/10.1002/slct.202300053
https://hal.science/hal-03971862

2022

Organometallic derivatives of decoquinate targeted toward toxoplasma gondii
Betts H. D., Ong Y. C., Anghel N., Keller S., Karges J., Voutsara N., Müller J., Manoury E., Blacque O., Cariou K., Hemphill A., Gasser G.
Organometallics 2022, 41(15), 2035-2041.
https://doi.org/10.1021/acs.organomet.2c00204
https://hal.science/hal-03727450

Synthesis, characterization and electrochemical behavior of new bis(fluoroalkyl) ferrocenylphosphonates and their tin tetrachloride complexes
Mechi H., Sanhoury M. A. K., Laribi F., Manoury E., Mastouri M., Raouafi N., Bousseksou A., Dhia M. T. B.
Journal of Organometallic Chemistry 2022, 957, 122178/1-9.
https://doi.org/10.1016/j.jorganchem.2021.122178
https://hal.archives-ouvertes.fr/hal-03576457

Core-crosslinked micelles with a poly-anionic poly(styrene sulfonate)-based outer shell made by RAFT polymerization
Wang H., Fliedel C., Manoury E., Poli R.
Polymer 2022, 243, 124640/1-9.
https://doi.org/10.1016/j.polymer.2022.124640
https://hal.archives-ouvertes.fr/hal-03574234

Molybdenum-, vanadium-, and tungsten-containing materials for catalytic applications
Agustin D., Pisk J.
Materials 2022, 15(5), 1720/1-3.
https://doi.org/10.3390/ma15051720
https://hal.archives-ouvertes.fr/hal-03592139

Interrupted intramolecular hydroaminomethylation of N-protected-2-vinyl anilines: Novel access to 3-substitued indoles or indoline-2-ols
Hochberger-Roa F., García-Ríos P. H., López-Cortés J. G., Ortega-Alfaro M. C., Daran J.-C., Gouygou M., Urrutigoïty M.
Molecules 2022, 27(3), 1074/1-12.
https://doi.org/10.3390/molecules27031074
https://hal.archives-ouvertes.fr/hal-03592301

Catalyst-free epoxy vitrimers based on transesterification internally activated by an α–CF3 group
Berne D., Cuminet F., Lemouzy S., Joly-Duhamel C., Poli R., Caillol S., Leclerc E., Ladmiral V.
Macromolecules 2022, 55(5), 1669–1679.
https://doi.org/10.1021/acs.macromol.1c02538
https://hal.archives-ouvertes.fr/hal-03583794

Heteroleptic dirhodium(II) complexes with redox-active ferrocenyl ligands: Synthesis, electrochemical properties, and redox-responsive chemoselectivity in carbene C−H insertion
Ruzhylo I., Sournia-Saquet A., Moreau A., Delord T., Manoury E., Poli R., Labande A.
European Journal of Inorganic Chemistry 2022, 2022(12), e202200033/1-10.
https://doi.org/10.1002/ejic.202200033
https://hal.archives-ouvertes.fr/hal-03528757

Synthesis of ferrocenyl phosphorhydrazone dendrimers
Caminade A.-M., Manoury E.
Encyclopedia Platform. MDPI: Bâle (Switzerland), 2022, Entry 23675.
https://encyclopedia.pub/entry/23675
https://hal.archives-ouvertes.fr/hal-03714158

Cobalt–carbon bonding in a salen-supported cobalt(IV) alkyl complex postulated in oxidative MHAT catalysis
Wilson C. V., Kim D., Sharma A., Hooper R. X., Poli R., Hoffman B. M., Holland P. L.
Journal of the American Chemical Society 2022, 144(23), 10361-10367.
https://doi.org/10.1021/jacs.2c02128
https://hal.archives-ouvertes.fr/hal-03689305

Synthesis and crystal structure of [(Sp)-(2-phenyl-ferrocen-yl)meth-yl]tri-methyl-ammonium iodide di-chloro-methane monosolvate
Lachguar A., Deydier E., Labande A., Manoury E., Poli R., Daran J. C.
Acta Crystallographica Section E 2022, 78(Pt 7), 722-726.
https://doi.org/10.1107/s2056989022006053
https://hal.archives-ouvertes.fr/hal-03737936

Understanding the reshaping of fluorinated polyester vitrimers by kinetic and DFT studies of the transesterification reaction
Lemouzy S., Cuminet F., Berne D., Caillol S., Ladmiral V., Poli R., Leclerc E.
Chemistry – A European Journal 2022, 28(48), e202201135/1-10.
https://doi.org/10.1002/chem.202201135
https://hal.archives-ouvertes.fr/hal-03689286

Coordination adaptable networks: zirconium(IV) carboxylates
Murali M., Berne D., Joly-Duhamel C., Caillol S., Leclerc E., Manoury E., Ladmiral V., Poli R.
Chemistry – A European Journal 2022, 28(61), e202202058/1-6.
https://doi.org/10.1002/chem.202202058
https://hal.archives-ouvertes.fr/hal-03739165

Phosphine-functionalized core-crosslinked micelles and nano-gels with an anionic poly(styrenesulfonate) shell: Synthesis, rhodium(I) coordination and aqueous biphasic hydrogenation catalysis
Wang H., Abou-Fayssal C. J., Fliedel C., Manoury E., Poli R.
Polymers 2022, 14(22), 4937/1-25.
https://doi.org/10.3390/polym14224937
https://hal.archives-ouvertes.fr/hal-03852403

Ring size-reactivity relationship in radical ring-opening copolymerisation of thionolactones with vinyl pivalate
Ivanchenko O., Mazières S., Poli R., Harrisson S., Destarac M.
Polymer Chemistry 2022, 13(45), 6284-6292
http://dx.doi.org/10.1039/D2PY01153K
https://hal.archives-ouvertes.fr/hal-03846177

Molybdenum, vanadium, and tungsten-based catalysts for sustainable (ep)oxidation
Pisk J., Agustin D.
Molecules 2022, 27(18), 6011/1-26.
https://doi.org/10.3390/molecules27186011
https://hal.archives-ouvertes.fr/hal-03877754

2021

Metal Complexes as Catalysts/Moderators for Polymerization Reactions
Fliedel C., Dagorne S., Le Roux E.
in Comprehensive Coordination Chemistry III, Constable E. C., Parkin G., Que Jr. L. (Eds.). Elsevier: Oxford, 2021, vol. 9, pp. 410-464. (978-0-12-409547-2).
https://doi.org/10.1016/B978-0-08-102688-5.00089-1
https://hal.archives-ouvertes.fr/hal-03594817

Recent representative advances on the synthesis and reactivity of N-heterocyclic-carbene-supported zinc complexes
Specklin D., Fliedel C., Dagorne S.
The Chemical Record 2021, 21(5), 1130-1143.
https://doi.org/10.1002/tcr.202100041
https://hal.archives-ouvertes.fr/hal-03204158

Chiral N-Heterocyclic Carbene-Based Ligands
César V., Fliedel C., Labande A.
in New Directions in Organic & Biological Chemistry Series. Chiral Ligands : Evolution of Ligand Libraries for Asymmetric Catalysis, Diéguez M. (Ed.). CRC Press: Boca Raton, 2021, pp. 195-232. (978-0-367-4-28488).
https://doi.org/10.1201/9780367855734-6
https://hal.archives-ouvertes.fr/hal-03230806

Implication of oxidant activation on olefin epoxidation catalysed by molybdenum catalysts with aroylhydrazonato ligands: Experimental and theoretical studies
Bafti A., Razum M., Topić E., Agustin D., Pisk J., Vrdoljak V.
Molecular Catalysis 2021, 512, 111764/1-12.
https://doi.org/10.1016/j.mcat.2021.111764
https://hal.archives-ouvertes.fr/hal-03356884

RAFT polymerisation of trifluoroethylene: the importance of understanding reverse additions
Bouad V., Guerre M., Totée, Silly G., Gimello O., Améduri B., Tahon J.-F., Poli R., Barrau S., Ladmiral V.
Polymer Chemistry 2021, 12(15), 2271-2281.
http://dx.doi.org/10.1039/D0PY01754J
https://hal.archives-ouvertes.fr/hal-03182909

Oxidation-promoted synthesis of ferrocenyl planar chiral rhodium(III) complexes for C–H functionalization catalysis
Cabanes J., Odnoroh M., Duhayon C., Bijani C., Sournia-Saquet A., Polia R., Labande A.
Mendeleev Communications 2021, 31(5), 620-623.
https://doi.org/10.1016/j.mencom.2021.09.010
https://hal.archives-ouvertes.fr/hal-03412564

Chiral Tridentate-Based Ligands
Bandyopadhyay U., Sundararaju B., Poli R., Manoury E.
in New Directions in Organic & Biological Chemistry Series. Chiral Ligands : Evolution of Ligand Libraries for Asymmetric Catalysis, Diéguez M. (Ed.). CRC Press: Boca Raton, 2021, pp. 167-194. (978-0-367-4-28488).
https://doi.org/10.1201/9780367855734-5
https://hal.archives-ouvertes.fr/hal-03230854

Amphiphilic polymeric nanoreactors containing Rh(i)–NHC complexes for the aqueous biphasic hydrogenation of alkenes
Salomon Sambou S., Hromov R., Ruzhylo I., Wang H., Allandrieu A., Sabatier C., Coppel Y., Daran J.-C., Gayet F., Labande A., Manoury E., Poli R.
Catalysis Science & Technology 2021, 11, 6811-6824.
http://dx.doi.org/10.1039/D1CY00554E
https://hal.archives-ouvertes.fr/hal-03171897

Synthesis and crystallographic studies of 2-(diphenylphosphinothioyl)-2-(3-oxobut-1-en-yl)ferrocene
Bandyopadhyay U., Sundararaju B., Poli R., Manoury E., Daran J.-C.
Acta Crystallographica Section E 2021, 77(8), 853-856.
https://doi.org/10.1107/S205698902100760X
https://hal.archives-ouvertes.fr/hal-03364269

Replacement of volatile acetic acid by solid sio2@COOH silica (nano)beads for (ep)oxidation using Mn and Fe complexes containing BPMEN ligand
Wang Y., Gayet F., Daran J.-C., Guillo P., Agustin D.
Molecules 2021, 26(18), 5435/1-26.
https://doi.org/10.3390/molecules26185435
https://hal.archives-ouvertes.fr/hal-03356932

New borrowing hydrogen mechanism for redox-active metals
Chakraborty P., Sundararaju B., Manoury E., Poli R.
ACS Catalysis 2021, 11, 11906-11920.
https://doi.org/10.1021/acscatal.1c02616
https://hal.archives-ouvertes.fr/hal-03244195

NMR investigations of polytrifluoroethylene (PTrFE) synthesized by RAFT
Bouad V., Guerre M., Zeliouche S., Améduri B., Totée C., Silly G., Poli R., Ladmiral V.
Polymer Chemistry 2021, 12(15), 2293-2304.
http://dx.doi.org/10.1039/D0PY01753A
https://hal.archives-ouvertes.fr/hal-03188630

Efficient molybdenum hydrazonato epoxidation catalysts operating under green chemistry conditions: Water vs. decane competition
Mrkonja S., Topić E., Mandarić M., Agustin D., Pisk J.
Catalysts 2021, 11(7), 756/1-14.
https://doi.org/10.3390/catal11070756
https://hal.archives-ouvertes.fr/hal-03267910

Rhodium nanoparticles inside well-defined unimolecular amphiphilic polymeric nanoreactors: synthesis and biphasic hydrogenation catalysis
Wang H., Fiore A. M., Fliedel C., Manoury E., Philippot K., Dell’Anna M. M., Mastrorilli P., Poli R.
Nanoscale Advances 2021, 3(9), 2554-2566.
http://dx.doi.org/10.1039/D1NA00028D
https://hal.archives-ouvertes.fr/hal-03176469

Triphenylphosphine-functionalized core-cross-linked micelles and nanogels with a polycationic outer shell: Synthesis and application in rhodium-catalyzed biphasic hydrogenations
Wang H., Vendrame L., Fliedel C., Chen S., Gayet F., D’Agosto F., Lansalot M., Manoury E., Poli R.
Chemistry – A European Journal 2021, 27(16), 5205-5214.
https://doi.org/10.1002/chem.202004689
https://hal.archives-ouvertes.fr/hal-03081418

A journey into metal–carbon bond homolysis
Poli R.
Comptes Rendus Chimie 2021, 24(1), 147-175.
https://doi.org/10.5802/crchim.73
https://hal.archives-ouvertes.fr/hal-3209704

Phospholylmethano P-chirogenic-phosphine-borane as P-(η2-BH3)-chelating ligands of rhodium (I): Synthesis, characterization and asymmetric hydrogenation
Salomon-Bertrand C., Bayardon J., Lauréano H., Jugé S., Daran J.-C., Gouygou M.
Journal of Organometallic Chemistry 2021, 938, 121753/1-7.
https://doi.org/10.1016/j.jorganchem.2021.121753
https://hal.archives-ouvertes.fr/hal-03202816

Well-defined PIII-terminated polymers from phosphorylated carbodithioate RAFT agents
Karpus A., Harrisson S., Poli R., Mazières S., Manoury E., Destarac M.
Macromolecules 2021, 54(6), 2627-2636.
https://doi.org/10.1021/acs.macromol.0c02805
https://hal.archives-ouvertes.fr/hal-03200586

Cobalt complexes of an OSNSO-tetrapodal pentadentate ligand: Synthesis, structures and reactivity
Thevenin L., Daran J.-C., Poli R., Fliedel C.
Inorganica Chimica Acta 2021, 518, 120215/1-8.
https://doi.org/10.1016/j.ica.2020.120215
https://hal.archives-ouvertes.fr/hal-03108199

Enhanced aminolysis of cyclic carbonates by β-hydroxylamines for the production of fully biobased polyhydroxyurethanes
Quienne B., Poli R., Pinaud J., Caillol S.
Green Chemistry 2021, 23(4), 1678-1690.
http://dx.doi.org/10.1039/D0GC04120C
https://hal.archives-ouvertes.fr/hal-03148901

Partnerships

Click here to consult the partners

Dr. Bruno Améduri, Dr. Vincent Ladmiral

Institut Charles Gerhardt (UMR 5253 CNRS)

Ingénierie et Architectures Macromoléculaires,

ENSCM, Place Eugène Bataillon,

34095 Montpellier, Cedex 5 (France)

bruno.ameduri@enscm.fr

vincent.ladmiral@enscm.fr

 

Prof. Ahmed Benharref

Laboratoire de chimie biomoléculaire, substances naturelles et réactivité,

Unité associée au CNRST (URAC16)

Université Cadi-Ayyad

Faculté des sciences Semlalia

BP 2390, boulevard My Abdellah

40000 Marrakech (Morocco)

benharref@uca.ac.ma

 

Dr. Stéphane Caillol

ICGM

Université Montpellier

CNRS, ENSCM

Montpellier (France)

Tel: +1-33-467144327

sylvain.caillol@enscm.fr

 

Prof. Jérôme Claverie

Département de Chimie

Université de Sherbrooke

2500, Blvd de l’Université

Faculté des sciences Semlalia

J1K2R1, Sherbrooke, Qc (Canada)

Tel: +1-819-821-7246

jerome.claverie@usherbrooke.ca

 

Dr. Franck D’Agosto, Dr. Muriel Lansalot

Chimie Catalyse Polymères et Procédés (C2P2)

Equipe LCPP (UMR 5265 CNRS/ESCPE/UCBLyon1)

CPE Lyon – 43, boulevard du 11 Novembre 1918

BP 2077

69616 Villeurbanne Cedex

Tel: +33-(0)472431770

franck.dagosto@univ-lyon1.fr

muriel.lansalot@univ-lyon1.fr.fr

 

Prof. Henri Delmas, Dr. Carine Julcour , Dr. Jean-François Blanco

CNRS, LGC (Laboratoire de Génie Chimique)

4 Allée Emile Monso

BP 84234

31030 Toulouse Cedex 4 (France)

henri.delmas@ensiacet.fr

carine.julcour@ensiacet.fr

jeanfrancois.blanco@ensiacet.fr

 

Prof. Mathias Destarac, Dr. Stéphane Mazières

CNRS, IMRCP UMR 5623,

Université Paul Sabatier

118 route de Narbonne, 31062 Toulouse (France)

destarac@chimie.ups-tlse.fr

mazieres@chimie.ups-tlse.fr

 

Dr. Christophe Detrembleur, Dr. Antoine Debuigne

Center for Education and Research on Macromolecules

University of Liege

Sart-Tilman B6

4000 Liege (Belgium)

Tel. +32 4 3663465

Fax. +32 4 3663497

christophe.detrembleur@ulg.ac.be

adebuigne@ulg.ac.be

 

Prof. Montserrat Diéguez

Universitat Rovira i Virgili

Campus Sescelades

Marcel·lí Domingo s/n

43007 Tarragona (Spain)

Tel. +34-977-558046 / 558627

Fax. +34-977-559563

montserrat.dieguez@urv.cat

 

Prof. Simon Duckett

Department of Chemistry

University of York

Heslington

York YO10 5DD (UK)

Tel. +44-1904-432564

Fax. +34-977-559563

sbd3@york.ac.uk

 

Prof. Norberto Farfán

Facultad de Química

Depto. de Química Orgánica

Universidad Nacional Autónoma de México

04510 México D.F., (Mexico)

norberto.farfan@gmail.com

 

Dr. Artem Guschchin

Nikolaev Institute of Inorganic Chemistry,

Siberian Branch of the Russian Academy
of Sciences,

3 Lavrentiev av., Novosibirsk, 630090 (Russia)

gushchin@niic.nsc.ru

 

Prof. Patrick Holland

Department of Chemistry,

Yale University,

New Haven, Connecticut 06511 (USA)

patrick.holland@yale.edu

 

Prof. Agustí Lledós

Departament de Química

Universitat Autònoma de Barcelona

Edifici Cn

08193 Bellaterra (Spain)

Tel: +34-935811716

Fax: +34-935812920

agusti@klingon.uab.es

 

Dr. Alexandr M. Kal’sin

  1. N. Nesmeyanov Labratory for Organometallic Chemistry

A.N. Nesmeyanov Institute of Organoelement Compounds

RAS 28 Vavilov Str.

Moscow (Russia)

kalsin@ineos.ac.ru

 

Prof. Piero Mastrorilli

DICATECh

Politecnico di Bari

via Orabona, 4

70125 Bari (Italy)

Tel: +39-080-5963605

pietro.mastrorilli@poliba.it

 

Prof. Krzysztof Matyjaszewski

Department of Chemistry

Carnegie Mellon University

4400 Fifth Ave.

Pittsburgh, PA 15213 (USA)

Tel: +1-412-268-3209

Fax: +1-412-268-6897

km3b@andew.cmu.edu

 

Prof. Jean-Luc Pirat, Prof. David Virieux

Ecole Nationale Supérieure de Chimie de Montpellier

8 rue de l’Ecole Normale

34296 Montpellier Cedex 5 (France)

Tel. +33-(0)467147243

jean-luc.pirat@enscm.fr

david.virieux@enscm.fr

 

Dr. Karine Philippot

Laboratoire de Chimie de Coordination

205 Route de Narbonne

31077 Toulouse (France)

Tel: +39-561333230

karine.philippot@lcc-toulouse.fr

 

Prof. Anders Riisager

Technical University of Denmark

Kemitorvet

Building 206, room 144

2800 Kgs. Lyngby (Denmark)

Tel: +45 45 25 22 33

ar@kemi.dtu.dk

 

Prof. Michael P. Shaver

School of Chemistry

University of Edinburgh

West Mains Road

Edinburgh, EH9 3JJ (UK)

Tel: +44 (0)131-6504726

michael.shaver@ed.ac.uk

 

Prof. Elena S. Shubina, Prof. Natalia V. Belkova

Laboratory of Metal Hydrides

A.N. Nesmeyanov Institute of Organoelement Compounds

RAS 28 Vavilov Str.

Moscow (Russia)

Tel: +7-095-1356448

Fax: +7-095-1355085

shu@ineos.ac.ru

nataliabelk@ineos.ac.ru

 

Prof. Basker Sundararaju

Department of Chemistry,

Indian Institute of Technology Kanpur,

Kanpur, 208016 (India)

basker@iitk.ac.in

 

Prof. Zoia Voitenko

Taras Shevchenko National University of Kyiv

Kyiv 01033 (Ukraine)

z_voitenko@ukr.net

 

Dr. Yong Wang

Key Laboratory for Material Chemistry of Energy Conversion and Storage,

Ministry of Education, School of Chemistry and
Chemical Engineering,

Huazhong University of Science and Technology, Wuhan 430074 (P. R. China)

tcwy@hust.edu.cn

 

Prof. Zhigang Xue

Key Laboratory for Material Chemistry of Energy Conversion and Storage,

Ministry of Education, School of Chemistry and
Chemical Engineering,

Huazhong University of Science and Technology, Wuhan 430074 (P. R. China)

zgxue@mail.hust.edu.cn

 

Prof. Carmen CLAVER, Prof. Cyril GODARD

Universitat Virgili i Rovira, Tarragona

Espagne.

 

Prof. José Guadalupe LOPEZ CORTES, Dr Maria del Carmen ORTEGA ALFARO

Université Autonome de Mexico (UNAM)

Mexico, Mexique.

 

Prof. Zoia VOITENKO

Université Nationale Taras Shevchenko de Kyiv, Ukraine

Prof. Vitaly KALCHENKO, Prof. Vyacheslav BOIKO

Institute of Organic Chemistry of the National Academy of Sciences of Ukraine

Kyiv, Ukraine.

 

Prof. Rafika BOUCHENE

Département Sciences de la Matière

Faculté des Sciences Exactes et des Sciences de la nature et de la vie

Université Larbi Ben M’hidi

Oum El Bouaghi, Algérie.

 

Dr. Med Abderrahmane SANHOURY

Université de Tunis El Manar

Tunisie.

 

Dr. Vincent César

Laboratoire de Chimie de Coordination

205 Route de Narbonne

31077 Toulouse (France)

Tel: +39-561333172

vincent.cesar@lcc-toulouse.fr

 

Prof. Süleyman Gülcemal, Prof. Derya Gülcemal

Department of Chemistry

Ege University

Bornova, 35100 Izmir, Turquie.

suleyman.gulcemal@ege.edu.tr

Funding

Click here to consult the funders
  • Agence Nationale de la Recherche. 2020-2024 (4 years). AAP générique 2019 No. ANR-19-CE06-0014-02. “Additive-Free Covalent Adaptable Networks (AFCAN)”. Sylvain Caillol (ICG Montpellier, Coordinator), Rinaldo Poli (PI) (449 813 € total; 178 740 € for the team).
  • Agence Nationale de la Recherche. 2019-2023 (4 years). AAP générique 2019 No. ANR-19-CE07-0043. “Redox modulation of dirhodium(II)-catalyzed nitrene insertions into C(sp3)-H bonds (CHamRhOx)”. Agnès Labande (LCC Toulouse, Coordinator), Eric Manoury (participant), Rinaldo Poli (participant) (360 439 € total; 179 388 € for the team).
  • Agence Nationale de la Recherche. 2020-2022 (3 years). AAP générique 2019 No. Contract No. ANR-19-CE07-0031-01. “Metal complexes for polymerization mechanism switching (POLYSWITCH)”. Christophe Fliedel (LCC Toulouse, Coordinator), Rinaldo Poli (participant) (187 164 €).
  • European Commission, Horizon2020, Marie Curie action “ITN-EJD”. Contract No. 860322. 2020-24 (4 years). European Joint Doctorate Training Network: “Coordination Chemistry Inspires Molecular Catalysis (CCIMC)” (3 977 588.16 €). Rinaldo Poli (Coordinator). Beneficiary institutions: CNRS-LCC, University of York, Universitat Autònoma Barcelona, Universitatea din Bucuresti, Universidad Rovira i Virgili, Uniwersytet Warszawski, Friedrich Schiller Universität Jena, Universität Leipzig, Danmarks Tekniske Univ. Partner institutions: IFP Energies nouvelles, Tecnalia, Henkel KGaA, Johnson Matthey PLC, Elkem Silicones France, Solvay, BASF.

 

LCC

Laboratoire de chimie de coordination du CNRS

205 route de Narbonne, BP 44099
31077 Toulouse cedex 4
France

+ 33 5 61 33 31 00