David SÉMERIL
Chargé de Recherche au CNRS
Year of creation of the group - 2018 (formerly LCIMC headed by D. Matt)
Le bel Institute, 9th floor South
Agnès REIFFSTECK
email : reiffste@unistra.fr
Phone : +33 (0)3 68 85 14 32
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PhD students
Post-docts
We are interested in the development of constrained ligands, with a particular emphasis upon the synthesis of cavity-shaped ligands, for organometallic catalysis and green chemistry catalysis.
Our team welcomes internship applications at the Master level, potential candidates interested in PhD studies as well as post-doctoral candidates.
Encapsulated Neutral Ruthenium Catalyst for Substrate- Selective Oxidation of Alcohols
Evaluation of the Catalytic Capability of cis‐ and trans‐Diquinoxaline Spanned Cavitands
Chiral calixarene and resorcinarene derivatives. Conical cavities substituted at their upper rim by two phosphito units and their use as ligands in Rh-catalysed hydroformylation
Catal. Commun., 118 (2019),70-75
Cavitand chemistry: nickel half-sandwich complexes with imidazolylidene ligands bearing one or two resorcinarenyl substituents
Substrate-selective olefin hydrogenation with a cavitand-based bis-N-anisyl-iminophosphorane
S. Hkiri, M. Steinmetz, R. Schurhammer, and D. Sémeril
Encapsulated Neutral Ruthenium Catalyst for Substrate- Selective Oxidation of Alcohols
Chem. Eur. J. 2022, 28, e202201887 – DOI : org/10.1002/chem.202201887
S. Hkiri, S. Touil, A. Samarat, D. Sémeril
Functionalized-1,3,4-oxadiazole ligands for the ruthenium-catalyzed Lemieux-Johnson type oxidation of olefins and alkynes in water
Molecular Catalysis 517 (2022) 112014 – DOI: https://doi.org/10.1016/j.mcat.2021.112014
S. Hkiri and D. Sémeril
How Do Positions of Phosphito Units on a Calix[4]Arene Platform Affect the Enantioselectivity of a Catalytic Reaction?
Organics 2022, 3, 470–480 – DOI: https://doi.org/10.3390/org3040030
M. Kaloğlu, N. Gürbüz, D. Sémeril, İ. Özdemir
Ruthenium(II)-(p-cymene)-N-Heterocyclic Carbene Complexes for the N-Alkylation of Amine Using the Green Hydrogen Borrowing Methodology
Eur. J. Inorg. Chem. (2018) 1236-1243
M. Teci, D. Hueber, P. Pale, L. Toupet, A. Blanc, E. Brenner, D. Matt
Metal Confinement through N-(9-Alkyl)fluorenyl Substituted N-Heterocyclic Carbenes and its Consequences in Gold-Catalysed Reactions Involving Enynes
Chemistry, Eur. J. (2017) 7809-7818
F. Elaieb, D. Sémeril, D. Matt, M. Pfeffer, P.-A. Bouit, M. Hissler, C. Gourlaouen, J. Harrowfield
Calix[4]arene-fused phospholes
Dalton Trans. (2017) 9833-9845
L. Monnerau, D. Sémeril, D. Matt, C. Gourlaouen
Catalytic behaviour of calixarenylphosphanes in nickel-catalysed Suzuki-Miyaura cross-coupling
Eur. J. Inorg. Chem. (2017) 581-586
T. S. Manikandan, R. Ramesh, D. Sémeril
Synthesis and characterisation of cycloruthenated benzhydrazone complexes: Catalytic application to selective oxidative cleavage of olefins to aldehydes
RSC Advances 6 (2016) 97107-97115
T. Chavagnan, D. Sémeril, D. Matt, J. Harrowfield, L. Toupet
Cracking Cavitands: Metal-Directed Scission of Phosphinyl-Substituted Resorcinarenes
Chem. Eur. J. 21 (2015) 6678-6681
D. Sémeril, D. Matt
Synthesis and catalytic relevance of P(III) and P(V)-functionalised calixarenes and resorcinarenes (Review)
Coord. Chem. Rev. 279 (2014) 58-95
A small overview of our research group