Abstract

An investigation into the CO-releasing properties of a range of iron tricarbonyl and chromium and molybdenum tetracarbonyl complexes is presented. Iron tricarbonyl complexes containing the 2,5-bicyclo[2.2.1]heptene (norbornadiene) ligand are shown to be effective CO-releasing molecules, in which the rate and extent of CO release may be modulated by modification of the norbornadiene framework. Species containing the parent norbornadiene and those with a substituent at the 7-position of the organic ligand exhibit CO release; those containing ester substituents at the 2- and/or 3-positions do not. A mechanism for CO release in this species is proposed which involves initial norbornadiene dissociation, a suggestion which is supported by the spectroscopic data and the observation that the addition of excess substituted norbornadiene retards the rate of CO release. CO release from the diester-containing norbornadiene complex may be promoted photochemically, and cell viability studies indicate that in the absenc...

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