Mono- and Bis-Cyclometalated Palladium Complexes: Synthesis, Characterization, and Catalytic Activity

被引:9
|
作者
Molitor, Sebastian [1 ]
Schwarz, Christopher [1 ]
Gessner, Viktoria H. [1 ]
机构
[1] Univ Wurzburg, Inst Anorgan Chem, Hubland, D-97074 Wurzburg, Germany
关键词
N-HETEROCYCLIC CARBENE; RAY CRYSTAL-STRUCTURE; C-H; REDUCTIVE ELIMINATION; COUPLING REACTIONS; DILITHIO METHANDIIDE; ELECTRONIC-STRUCTURE; OXIDATIVE ADDITION; LIGAND COOPERATION; OLEFIN METATHESIS;
D O I
10.1021/acs.organomet.5b00903
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cyclometalated palladium complexes have found a variety of applications, above all in homogeneous catalysis. Most complexes include mono-cyclometalated ligands, particularly systems with P- or N-donors. Herein, we report the preparation of a series of mono- and bis-cyclometalated palladium complexes with a silyl-substituted thiophosphinoyl ligand. The complexes have been synthesized via oxidative addition and dehydrohalogenation reactions. Thereby, dehydrohalogenation selectively results in the second cyclometalation and not in the formation of a carbene species. In the formed square-planar palladacycles the ligands exhibit S,C- and S,C,C-coordination modes, respectively. Depending on the silyl moiety, cyclometalation occurs via an aryl or even a methyl group, thus also giving way to unusual silapalladacyclobutanes with an open-book geometry. The complexes have been characterized in solution as well as in the solid state. Preliminary catalytic studies show that both the mono- and bis-cydometalated complexes can be applied as catalysts in C-C coupling reactions.
引用
收藏
页码:159 / 167
页数:9
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