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Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
An unprecedented high nuclearity catecholato-based Ti(IV)-architecture bearing labile pyridine ligands
Clément Chaumont1, Pierre Mobian, Marc Henry
1Laboratoire de Chimie Moléculaire de l'Etat Solide, UMR 7140, Université de Strasbourg, 67070 Strasbourg, France. mobian@unistra.fr henry@unistra.fr.
Abstract:
We describe the synthesis and characterisation of a robust S4-symmetry titanium-based architecture bearing catecholato and pyridine ligands. This neutral complex formulated as [Ti10O12(cat)8(py)8] displays a tetrahedral inorganic core decorated by catecholato ligands with unusual coordination modes. In solution, the pyridine ligands are labile as shown in DOSY studies at variable temperature. The light absorption property in the visible domain (λmax = 411 nm, ε = 10 800) was also characterised for the complex.
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