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[SRCO] Synthèse, Réactivité et Catalyse Organométalliques

Head of the research group

Samuel DAGORNE
Directeur de Recherche au CNRS

Location

Le Bel Institute, 9th floor North

Secretarial and accounting services provided by

Agnès REIFFSTECK
email: reiffste@unistra.fr
Phone : +33 (0)3 68 85 14 32

Permanent members

  • Samuel DAGORNE
    Directeur de Recherche CNRS
    email: dagorne@unistra.fr
    Phone: +33 (0)3 68 85 15 30
  • Béatrice JACQUES
    Maître de Conférence Unistra
    email: jacques@unistra.fr
    Phone: +33 (0)3 68 85 10 87
   

Non-permanent members

PhD student

  • Satawat Tongdee

PostDocs

  • Sandip Munshi
  • Geetika Gupta

Guest Prof. (2 months per year since 2017, 6 months in 2024):

  • Pr. Rudi Wehmschulte (Florida Tech)

Description of the group

The SRCO team broadly aims at the design and reactivity of novel organometallic complexes for small molecules activation (H2, CO2) and use in homogeneous catalysis, with a special emphasis on sustainable catalytic processes. 

Past/current industrial colloborations: Corbion-Purac Corp. (lactide polymerization), SNF Corp. (biodegradable hydrophilic polymers)

Our team welcomes internship applications at the Master level, potential candidates interested in PhD studies as well as post-doctoral candidates.   

Research topics

  • Low-coordinated oxophilic metal species (essentially with groups 2, 12 and 13 metal centers), in particular supported by N-heterocyclic carbenes (NHCs),
  • Small molecules (H2, CO2) activation (H2, CO2) with highly electrophilic organometallics based on Al(III), Zn(II) and Mg(II) salts,
  • Polymerization catalysis of cyclic esters/carbonates using organometallics for the production of biomaterials,
  • Organometallic complexes of Au(I)/Au(III) for use in homogeneous catalysis.

Zn-carbonate

thèmes de recherche

Enseignement

Vous trouverez ci-dessous les 3 premiers cours M1 du Dr Samuel Dagorne.

Vous trouverez ci-dessous les cours L3 du Dr Samuel Dagorne.

Selection of key publications

G. Printz, D. Ryzhakov , C. Gourlaouen , B. Jacques, S. Messaoudi, F. Dumas, F. Le Bideau, S. Dagorne
First Use of Thiosquaramides as Polymerization Catalysts: Controlled ROP of Lactide Implicating Key Secondary Interactions for Optimal Performance
ChemCatChem 202416 (1), e202301207– DOI :  https://doi.org/10.1002/cctc.202301207.

X. Xu, C. Gourlaouen, B. Jacques, S. Dagorne
Robust Two-Coordinate Zn(II) Organocations Supported by Bulky-Yet-Flexible IPr* Carbene: Synthesis, Structure, and Distinct Reactivity in Hydrosilylation Catalysis. Organometallics 202342 (19), 2813–2825– DOI :   https://doi.org/10.1021/acs.organomet.3c00282

P. de Frémont, N. Adet, J. Parmentier, X. Xu, B. Jacques, S. Dagorne
Cationic Organometallic Complexes of Group 12 Metals: A Decade of Progress toward the Quest of Novel Lewis Acidic Catalysts
Coordination Chemistry Reviews 2022469, 214647– DOI :   https://doi.org/10.1016/j.ccr.2022.214647.

J. Tian, Y. Chen, M. Vayer, A. Djurovic, R. Guillot, R. Guermazi, S. Dagorne, C. Bour, V. Gandon
Exploring the Limits of π‐Acid Catalysis Using Strongly Electrophilic Main Group Metal Complexes: The Case of Zinc and Aluminium
Chem. Eur. J. 26 (2020) 12831–12838 – DOI : https://doi.org/10.1002/chem.202001376

N. Adet, D. Specklin, C. Gourlaouen, T. Damiens, B. Jacques, R.J. Wehmschulte, S. Dagorne
Towards Naked Zinc(II) in the Condensed Phase: A Highly Lewis Acidic ZnII Dication Stabilized by Weakly Coordinating Carborate Anions
Angewandte Chemie International Edition,
Early view – DOI : https://doi.org/10.1002/anie.202012287

Y.C.A. Sokolovicz, O. Nieto Faza, D. Specklin, B. Jacques, C.S. López, J.H.Z. dos Santos, H.S. Schrekker, S. Dagorne
Acetate-catalyzed hydroboration of CO 2 for the selective formation of methanol-equivalent products
Catalysis Science & Technology,
10 (2020) 2407–2414 - DOI : https://doi.org/10.1039/D0CY00118J

A.T. Normand, R. Malacea-Kabbara, R. Lapenta, A. Dajnak, P. Richard, H. Cattey, A. Bolley, A. Grassi, S. Milione, A. Auffrant, S. Dagorne, P. Le Gendre
Phosphasalen group IV metal complexes: synthesis, characterization and ring opening polymerization of lactide, Dalton Transactions, 49 (2020) 6989–7004 - DOI : https://doi.org/10.1039/D0DT00972E

C. Romain, S. Bellemin-Laponnaz, S. Dagorne
Recent progress on NHC-stabilized early transition metal (group 3–7) complexes: Synthesis and applications
Coordination Chemistry Reviews
, 422 (2020) 213411 - DOI : https://doi.org/10.1016/j.ccr.2020.213411

Bruyere, J.-C.; Specklin, D.; Gourlaouen, C.; Lapenta, R.; Veiros, L. F.; Grassi, A.; Milione, S.; Ruhlmann, L.; Boudon, C.; Dagorne, S.
Cyclic(Alkyl)(Amino)Carbene (CAAC)-Supported Zn Alkyls: Synthesis, Structure and Reactivity in Hydrosilylation Catalysis
Chemistry – A European Journal
2019, 25 (34), 8061–8069 - DOI: https://doi.org/10.1002/chem.201900961
Cover feature:
S. Dagorne et al.

Bruyere, J.-C.; Gourlaouen, C.; Karmazin, L.; Bailly, C.; Boudon, C.; Ruhlmann, L.; de Frémont, P.; Dagorne, S.
Synthesis and Characterization of Neutral and Cationic Magnesium Complexes Supported by NHC Ligands
Organometallics 2019, 38 (14), 2748–2757 - DOI:  https://doi.org/10.1021/acs.organomet.9b00304

Dagorne, S.
Recent Developments on N-Heterocyclic Carbene Supported Zinc Complexes: Synthesis and Use in Catalysis
Synthesis 2018, 50 (18), 3662–3670 - DOI:  https://doi.org/10.1055/s-0037-1610088

Dagorne, S. Wehmschulte, R.
Recent Developments on the Use of Group 13 Metal Complexes in Catalysis
ChemCatChem 2018, 10 (12), 2509–2520 - DOI: http://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.201800045

D. Specklin, F. Hild, C. Fliedel, C. Gourlaouen, L. F. Veiros, S. Dagorne
Accessing Two‐Coordinate ZnII Organocations by NHC Coordination: Synthesis, Structure, and Use as π‐Lewis Acids in Alkene, Alkyne, and CO2 Hydrosilylation
Chem. Eur. J.
2017, 23, 15908-15912- DOI: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201704382

D. Specklin, C. Fliedel, C. Gourlaouen, J.-C. Bruyere, T. Avilés, C. Boudon, L. Ruhlmann, S. Dagorne
N‐Heterocyclic Carbene Based Tri‐organyl‐Zn–Alkyl Cations: Synthesis, Structures, and Use in CO2 Functionalization
Chem. Eur. J.
2017, 23, 5509-5519 - DOI: https://www.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201605907