Synthesis and Properties of NHC-Supported Palladium(I) Dimers with Bridging Allyl, Cyclopentadienyl, and Indenyl Ligands

被引:17
作者
Dai, Wei [1 ]
Chalkley, Matthew J. [1 ]
Brudvig, Gary W. [1 ]
Hazari, Nilay [1 ]
Melvin, Patrick R. [1 ]
Pokhrel, Ravi [1 ]
Takase, Michael K. [1 ]
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
基金
美国国家科学基金会;
关键词
METAL PI-COMPLEXES; EFFECTIVE CORE POTENTIALS; ORDER REGULAR APPROXIMATION; PD-PD; MOLECULAR CALCULATIONS; ETA-3-INDENYL LIGANDS; BINUCLEAR COMPLEXES; OXIDATIVE ADDITION; CRYSTAL-STRUCTURE; EXCHANGE-ENERGY;
D O I
10.1021/om400687m
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of a family of new Pd(I) dimers, (mu-All)(mu-Cp){Pd(IPr)}(2) (All = C3H5, Cp = C5H5, IPr = 1,3-bis(2,6-diisopropylphenyl)-1,3-dihydro-2H-imidazol-2-yli-dene), (mu-All)(mu-Ind){Pd(IPr)}(2) (Ind = C7H9), (mu-Cp)(mu-Cp){Pd(IPr)}(2), (mu-Cp)(mu-Ind){Pd(IPr)}(2), and (mu-Ind)(mu-Ind){Pd(IPr)}(2), which contain a combination of bridging ally!, Cp, and indenyl ligands and are all supported by IPr as the ancillary ligand, is reported. All of these compounds are thermally stable at room temperature, and the solid-state geometries, electronic structures, reactivity, and redox chemistry of these new compounds have been compared with those of the dimer (mu-All)(2){Pd(IPr)}(2), which was previously reported. This work provides further evidence that bridging allyl, Cp, and indenyl ligands bind in a similar manner to Pd(I). However, it is demonstrated that there are notable differences between the IPr-supported species and related Pd(I) diners with triethylphosphine ancillary ligands, which have been previously described.
引用
收藏
页码:5114 / 5127
页数:14
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