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Catherine Wieser

Researcher at Centre national de la recherche scientifique

Publications -  8
Citations -  487

Catherine Wieser is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Catalysis & Supramolecular chemistry. The author has an hindex of 6, co-authored 8 publications receiving 477 citations.

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Calixarene and resorcinarene ligands in transition metal chemistry

TL;DR: In this paper, an exhaustive review of calixarenes containing transition metals is presented, with a focus on synthetic aspects, to allow the reader to acquire a useful knowledge of the construction of transition metal complexes derived from calixarens.
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Capping calixarenes with metallodiphosphine fragments: towards intracavity reactions

TL;DR: The co-ordinative properties of four disubstituted compounds have been investigated in this paper, and the results showed that these act as internal solvent molecules in promoting the chelate complexes.
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Extractive properties towards rare-earth metal ions of calix[ 4] arenes substituted at the narrow rim by phosphoryl and amide groups

TL;DR: In this paper, the extractive properties of the cone and partial-cone isomers of 5,11,17,23,tetra-?ert-butyl-25,27-bis( diethylcarbamoylmethoxy)-26,28-bisi( diphenylphospninoyl methoxy) calyx arene ( cone-1 and partialcone -1) in 1,2-dichloroethane towards rare-earth metal ions in nitrate media at 25 ° C were investigated.
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Complexation Studies with a Calix[4]arene‐Derived Phosphinite − Divergent Arrays of Cavities Linked by MCl2 Fragments (M = Pd, Pt)

TL;DR: A cone-shaped calix[4]arene-derived monophosphinite, 25,27-di(ethoxycarbonylmethoxy)-26-hydroxy-28-(diphenylphosphinooxy)calix[ 4]-arene (L1), has been prepared in two steps from calix [4]AREne as mentioned in this paper.
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Hybrid ligands: synthesis, characterization and co-ordinative propertiesof a mixed phosphine–β-ketophosphorus ylide

TL;DR: In this paper, the structure of the resultant ylide was shown to be a 1:1 mixture of two rotamers built around the C(O) axis, the P-monodentate complex and the nickel complexes, where the hybrid ligand is P,O-bonded to the p-position.