Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Pierrette Battioni"'
Publikováno v:
European Journal of Inorganic Chemistry. 2007:2426-2433
The first iron complexes of the tetracationic 2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetra-N-pyridiniumylporphyrin, (OEPy4P)4+, in which four pyridine molecules are attached to the meso-carbon atoms through their nitrogen atoms, were synthesized in
Autor:
Delphine Mathieu, Daniel Mansuy, Irene Vitali, Pierrette Battioni, Alessandra Molinari, Elena Ganzaroli, Andrea Maldotti
Publikováno v:
European Journal of Inorganic Chemistry. 2004:3127-3135
Photochemical excitation (λ > 350 nm) of chloro[meso-tetrakis(2,6-dichlorophenyl)porphyrin]iron(III) [FeIII(TDCPP)Cl] and chloro[meso-tetra(α,α,α,α-pivalamidophenyl)porphyrin]iron(III) [FeIII(TpivPP)Cl] induces the oxidation of coordinated N-(4-
Autor:
Pierrette Battioni, Jean François Bartoli, Nathalie Pons-Y-Moll, Daniel Mansuy, Frédéric Banse, Delphine Mathieu, Jean-Jacques Girerd, Véronique Balland
Publikováno v:
Journal of Molecular Catalysis A: Chemical
Journal of Molecular Catalysis A: Chemical, Elsevier, 2004, 215, pp.81-87
Journal of Molecular Catalysis A: Chemical, Elsevier, 2004, 215, pp.81-87
Four iron(II) complexes, bearing hexa-, penta- or tetra-azadentate ligands, whose redox potentials (for the FeIII/FeII couple) vary from +280 to +1023 mV (versus saturated calomel electrode), were compared as catalysts for the oxidation of various su
Publikováno v:
Journal of Porphyrins and Phthalocyanines. :265-278
Data from the last few years have revealed a novel biological role of the tetrahydrobiopterin ( H4B ) cofactor, in one-electron transfers to the heme of the active site of NO-synthases (NOSs) with intermediate formation of a H4B -derived radical. The
Autor:
Jean-François Bartoli, Frédéric Banse, Tony A. Mattioli, Jean-Jacques Girerd, Daniel Mansuy, Marie-France Charlot, Pierrette Battioni, Véronique Balland, Eckhard Bill
Publikováno v:
European Journal of Inorganic Chemistry. 2004:301-308
Mononuclear FeIV intermediates have been generated in MeOH upon reaction of sodium hypochlorite or hypobromite with a ferrous complex bearing the pentadentate ligands N-methyl-N,N′,N′-tris(2-pyridylmethyl)ethane-1,2-diamine (L52) or N-methyl-N,N
Autor:
Jean-François Bartoli, François Lambert, Daniel Mansuy, Irène Morgenstern-Badarau, Pierrette Battioni
Publikováno v:
Comptes Rendus Chimie. 5:263-266
The non-heme iron complex, Fe(TPAA = tris-〚N-(2-pyridylmethyl)-2-aminoethyl〛amine)(ClO4)2, is a bad catalyst for the epoxidation of alkenes such as cyclooctene, cyclohexene and cis-stilbene and for the hydroxylation of alkanes such as adamantane
Publikováno v:
Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry. 3:751-755
Preparative hydroxylation of aromatic compounds such as drugs remain a difficult challenge. Here we show that the two main human metabolites of the anti-inflammatory drug diclofenac, 5-hydroxy- and 4′-hydroxy-diclofenac, can be prepared from diclof
Autor:
Pierrette Battioni, Alessandra Molinari, Rossano Amadelli, Daniel Mansuy, L. Antolini, Andrea Maldotti
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 158:521-531
Surface derivatization of titanium dioxide nanoparticles with a Fe(III)–porphyrin has been carried out following a new procedure whereby the complex, rather than the surface, contains the aminopropylsilane functional group. This avoids the problems
Autor:
Annah Mancy, Marie Antignac, Virginie Mouries, Patrick M. Dansette, Daniel Mansuy, Sylvie Dijols, Nguyet-Thanh Ha Duong, Claire Minoletti, Pierrette Battioni
Publikováno v:
Biochemistry. 38:14264-14270
A comparison of the oxidations of diclofenac with microsomes of yeasts expressing various human liver cytochromes P450 showed that P450 2C9 regioselectively led to 4'-hydroxy diclofenac (4'-OHD) whereas P450 3A4 only led to 5-hydroxy diclofenac (5-OH
Publikováno v:
Journal of the American Chemical Society. 120:12524-12530
Various iron porphyrin systems were found to catalyze the dehydration of aldoximes, such as heptanaldoxime or phenylacetaldoxime, into the corresponding nitriles under mild conditions (t = 20 °C, neutral or slightly acidic pH). In all these systems,