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
MANOURY Eric
DEYDIER Eric
ABOU FAYSSAL Chantal
AGUSTIN Dominique
AMBERT Dorian
AUDIN Catherine
BACQUE Cecilia
BEZVUHLIAK Yuliia
BIBAL-KOEPKE Christine
DARAN Jean-Claude
FAGUÉ Vincent
FLIEDEL Christophe
FORGET Laurianne
GARG Nidhi
GUILLO Pascal
HAIDAR Ali Alhadi
HARB Jana
KISTEN Paven
LABANDE Agnes
MASSOU Stephane
MICHELAS Maxime
MURALI Meenu
POLI Rinaldo
PULIDO DIAZ Israel
RAZA Arsen
RUZHYLO Illia
STEPHEN Treesa
VINCENDEAU Sandrine
VOROZHBIAN Anna
YANG Runqian
ZEROUGH Izid-bih
No Results Found
Research topics
Ligands and complexes
Complex architectures
Catalysis
Team news
Chemistry goes green.
Listen to the podcast “Les Deux Font La Paire”
recorded on the occasion of the Researchers’ Night 2022.
Publications
2023
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,
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,
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
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)
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)
ICGM
Université Montpellier
CNRS, ENSCM
Montpellier (France)
Tel: +1-33-467144327
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
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)
jeanfrancois.blanco@ensiacet.fr
Prof. Mathias Destarac, Dr. Stéphane Mazières
CNRS, IMRCP UMR 5623,
Université Paul Sabatier
118 route de Narbonne, 31062 Toulouse (France)
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
Universitat Rovira i Virgili
Campus Sescelades
Marcel·lí Domingo s/n
43007 Tarragona (Spain)
Tel. +34-977-558046 / 558627
Fax. +34-977-559563
Department of Chemistry
University of York
Heslington
York YO10 5DD (UK)
Tel. +44-1904-432564
Fax. +34-977-559563
Facultad de Química
Depto. de Química Orgánica
Universidad Nacional Autónoma de México
04510 México D.F., (Mexico)
Nikolaev Institute of Inorganic Chemistry,
Siberian Branch of the Russian Academy
of Sciences,
3 Lavrentiev av., Novosibirsk, 630090 (Russia)
Department of Chemistry,
Yale University,
New Haven, Connecticut 06511 (USA)
Departament de Química
Universitat Autònoma de Barcelona
Edifici Cn
08193 Bellaterra (Spain)
Tel: +34-935811716
Fax: +34-935812920
Dr. Alexandr M. Kal’sin
A.N. Nesmeyanov Institute of Organoelement Compounds
RAS 28 Vavilov Str.
Moscow (Russia)
DICATECh
Politecnico di Bari
via Orabona, 4
70125 Bari (Italy)
Tel: +39-080-5963605
Department of Chemistry
Carnegie Mellon University
4400 Fifth Ave.
Pittsburgh, PA 15213 (USA)
Tel: +1-412-268-3209
Fax: +1-412-268-6897
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
Laboratoire de Chimie de Coordination
205 Route de Narbonne
31077 Toulouse (France)
Tel: +39-561333230
karine.philippot@lcc-toulouse.fr
Technical University of Denmark
Kemitorvet
Building 206, room 144
2800 Kgs. Lyngby (Denmark)
Tel: +45 45 25 22 33
School of Chemistry
University of Edinburgh
West Mains Road
Edinburgh, EH9 3JJ (UK)
Tel: +44 (0)131-6504726
Prof. Elena S. Shubina, Prof. Natalia V. Belkova
A.N. Nesmeyanov Institute of Organoelement Compounds
RAS 28 Vavilov Str.
Moscow (Russia)
Tel: +7-095-1356448
Fax: +7-095-1355085
Prof. Basker Sundararaju
Department of Chemistry,
Indian Institute of Technology Kanpur,
Kanpur, 208016 (India)
Prof. Zoia Voitenko
Taras Shevchenko National University of Kyiv
Kyiv 01033 (Ukraine)
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)
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
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- 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
