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Synthesis and complexation properties of novel triazoyl-based ferrocenyl ligands
Authors:Gilles Gasser  Jonathan D Carr  Stephen J Green  Sean M Cafferkey  James HR Tucker
Institution:a Institute of Chemistry, University of Neuchâtel, Av. de Bellevaux 51, CH-2009 Neuchâtel, Switzerland
b School of Chemistry, University of Exeter, Stocker Road, Exeter EX4 4QD, UK
c School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, UK
d School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK
Abstract:Two new ligand derivatives of ferrocene, namely N-4-3,5-di-(2-pyridyl)-1,2,4-triazoyl]ferrocene carbimine (L1) and N-4-3,5-di-(2-pyridyl)-1,2,4-triazoyl]ferrocene carbamide (L2), were synthesised in good yields by reacting the known compound 3,5-di-pyridine-2-yl-1,2,4]triazol-4-ylamine (1) with ferrocenecarbaldehyde and chlorocarbonyl ferrocene, respectively. The structures of L1 and L2 were determined by X-ray crystallography. The complexation of L1 and L2 with CuI, AgI, ZnII and CdII was studied by NMR and UV-vis spectroscopies, as well as by electrochemistry, with titrations used to determine metal:ligand stoichiometries. The cyclic voltammograms of L1 and L2 and their respective complexes indicated reversible one-electron transfers corresponding to the Fc0/+ redox couple (Fc = ferrocene), with formal electrode potentials shifting to more positive values upon metal complexation.
Keywords:Self-assembly  Supramolecular chemistry  [2   ×     2] Grids  Ferrocene  N ligands
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