Flexible and Versatile Pincer-Type PGeP and PSnP Ligand Frameworks

被引:45
作者
Bestgen, Sebastian [1 ]
Rees, Nicholas H. [1 ]
Goicoechea, Jose M. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Dept Chem, 12 Mansfield Rd, Oxford OX1 3TA, Oxon, England
关键词
HETEROCYCLIC-CARBENE COMPLEXES; COORDINATION CHEMISTRY; METAL-COMPLEXES; NICKEL; BIS(SILYLENE); PHOSPHENIUM; REACTIVITY; PHOSPHORUS; ACTIVATION; CATALYSIS;
D O I
10.1021/acs.organomet.8b00698
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We describe the synthesis and application of two phosphine-functionalized pincer-type N-heterocyclic carbene analogues [(PNNP)E] (E = Ge, Sn) and their reactivity toward main group and precious metal compounds. These flexible tetrelene ligands feature unusual coordination geometries and strong P-E interactions and are expandable to digermylene or distannylene compounds on reaction with ECl2. The compounds were also successfully applied as ligands for the synthesis of Cu, Ag, Au, and Pt complexes. The inherent flexibility of the ligand scaffold enabled different structural arrangements driven by the coordination requirements of the metal centers and intermetallic interactions.
引用
收藏
页码:4147 / 4155
页数:9
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