Doubly Cyclometalated Pyridazines: Contrasting Behavior with Palladium and Platinum
journal contributionposted on 11.09.2001 by Jonathan W. Slater, Donocadh P. Lydon, Nathaniel W. Alcock, Jonathan P. Rourke
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The cyclometalation of 3,6-diphenylpyridazines with palladium and platinum has been studied. When palladium acetate is used as the metal source, two sequential cyclometalations are observed, with the first cyclometalation deactivating the system toward a second cyclometalation. Both monocyclopalladated and dicyclopalladated species have been isolated and characterized as their acetylacetonate derivatives. When potassium tetrachloroplatinate is used as the metal source, only double cycloplatination is observed: the first cycloplatination activates the system toward a second cycloplatination through a combination of nitrogen coordination and a chloride bridging two platinums. A doubly cycloplatinated compound has been isolated as its triphenylphosphine derivative, which has been fully characterized: the single-crystal X-ray structure shows that the two platinums are bridged by a chloride.