Bis-NHC Chelate Complexes of Nickel(0) and Platinum(0)

被引:28
作者
Brendel, Matthias [1 ]
Braun, Carolin [1 ]
Rominger, Frank [1 ]
Hofmann, Peter [1 ,2 ]
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
[2] Catalysis Res Lab CaRLa, D-69120 Heidelberg, Germany
关键词
carbene ligands; chelates; nickel; platinum; N-HETEROCYCLIC CARBENES; CARBON BOND-CLEAVAGE; C-F; STRUCTURAL-CHARACTERIZATION; MOLECULAR-STRUCTURE; OXIDATIVE ADDITION; METAL-COMPLEXES; ACTIVATION; PALLADIUM; REACTIVITY;
D O I
10.1002/anie.201401024
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For a long time d(10)-ML2 fragments have been known for their potential to activate unreactive bonds by oxidative addition. In the development of more active species, two approaches have proven successful: the use of strong sigma-donating ligands leading to electron-rich metal centers and the employment of chelating ligands resulting in a bent coordination geometry. Combining these two strategies, we synthesized bis-NHC chelate complexes of nickel(0) and platinum(0). Bis(1,5-cyclooctadiene) nickel(0) and -platinum(0) react with bisimidazolium salts, deprotonated in situ at room temperature, to yield tetrahedral or trigonal-planar bis-NHC chelate olefin complexes. The synthesis and characterization of these complexes as well as a first example of C-C bond activation with these systems are reported. Due to the enforced cis arrangement of two NHCs, these compounds should open interesting perspectives for bond-activation chemistry and catalysis.
引用
收藏
页码:8741 / 8745
页数:5
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