Doubly Cyclometalated Pyridazines: Contrasting Behavior with Palladium and Platinum
摘要:
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.
作者:Jonathan W Slater、Donocadh P Lydon、Jonathan P Rourke
DOI:10.1016/s0022-328x(01)01330-4
日期:2002.2
The mono and dicyclopalladation of new mesogenic pyridazines and subsequent reaction with beta-diketones yields some novel metallomesogens. The monometallated derivatives have a flat central core. In contrast. the dimetallated derivatives have a sterically induced twist in the molecule that renders them chiral. Smectic A phases are typically exhibited by both the derivatives with transition temperatures in the region of 100-300 degreesC. (C) 2002 Elsevier Science B.V. All rights reserved.