J
Jean-Louis Pierre
Researcher at Centre national de la recherche scientifique
Publications - 179
Citations - 5416
Jean-Louis Pierre is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Ligand & Copper. The author has an hindex of 40, co-authored 179 publications receiving 5165 citations. Previous affiliations of Jean-Louis Pierre include Joseph Fourier University.
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Journal ArticleDOI
Iron and activated oxygen species in biology: The basic chemistry
Jean-Louis Pierre,Marc Fontecave +1 more
TL;DR: A critical review concerning the chemical reactions involved when superoxide or hydrogen peroxide meet iron complexes is presented.
Journal ArticleDOI
Old iron, young copper: from Mars to Venus.
TL;DR: It is concluded that the early chemistry of life used water soluble ferrous iron while copper was in the water-insoluble Cu(I) state as highly insoluble sulphides, and copper, now bioavailable, was ideally suited to exploit the oxidizing power of dioxygen.
Journal ArticleDOI
pH-controlled change of the metal coordination in a dicopper(II) complex of the ligand H-BPMP: crystal structures, magnetic properties, and catecholase activity.
Stéphane Torelli,Catherine Belle,Isabelle Gautier-Luneau,Jean-Louis Pierre,Eric Saint-Aman,Jean-Marc Latour,L. Le Pape,Dominique Luneau +7 more
TL;DR: The results indicate that the pH dependence of the catalytic abilities of the complexes is related to changes in the coordination sphere of the metal centers.
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Imidazolate-bridged dicopper(II) and copper-zinc complexes of a macrobicyclic ligand (cryptand). A possible model for the chemistry of Cu-Zn superoxide dismutase
Jean-Louis Pierre,Pierre Chautemps,Sidi M. Refaif,Claude Béguin,Abdelilah El Marzouki,Guy Serratrice,Eric Saint-Aman,Paul Rey +7 more
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Efficient and Highly Selective Oxidation of Primary Alcohols to Aldehydes by N-Chlorosuccinimide Mediated by Oxoammonium Salts.
TL;DR: Very high chemoselectivities are observed when primary alcohols are oxidized in the presence of secondary ones, and primary-secondary diols are selectively transformed into hydroxy aldehydes, with, in some cases, no detectable formation of the isomeric keto alcohols.