化学
钯
有机钯
配体(生物化学)
催化作用
结晶学
有机化学
生物化学
受体
作者
Toshina Ukai,Hiroshi Kawazura,Yoshio Ishii,J. J. Bonnet,James A. Ibers
标识
DOI:10.1016/s0022-328x(00)91277-4
摘要
Recrystallization of bis(dibenzylideneacetone)palladium from various solvents affords novel binuclear palladium-dibenzylideneacetone complexes of composition Pd2(Dibenzylideneacetone)3(Solvent). These new complexes were identified by spectroscopic (IR, NMR, UV, and mass) and thermogravimetric analyses, together with a confirmative crystallographic structure determination. The CC bonds of a given dibenzylideneacetone ligand coordinate separately to two palladium atoms to yield a binuclear complex in which each palladium atom exhibits trigonal coordination. The Pd—Pd distance is 3.245 Å. Ligand exchange reactions, oxidative addition reactions, and complex formation reactions with p- and o-quinones were investigated and found to yield a variety of new organopalladium complexes.
科研通智能强力驱动
Strongly Powered by AbleSci AI