Synthesis and characterization of tetrapodal nickel complexes with adaptable ligand binding geometries.
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This study explores the versatile binding properties of a tetrapodal ligand framework with nickel, demonstrating significant ligand fluxionality through the interconversions of several complexes. Kinetic studies using UV-vis and NMR techniques underscore the pivotal role of solvent coordination in initiating these dynamic processes. A unique reverse-dative Ni Ag interaction provides another approach in modifying nickel's geometry.