Synthesis and characterisation of nonclassical ruthenium hydride complexes containing chelating bidentate and tridentate phosphine ligands

被引:60
作者
Prechtl, Martin H. G.
Ben-David, Yehoshoa
Giunta, Daniela
Busch, Stefan
Taniguchi, Yuki
Wisniewski, Wolfgang
Goerls, Helmar
Mynott, Richard J.
Theyssen, Nils
Milstein, David
Leitner, Walter
机构
[1] Univ Aachen, Rhein Westfal TH Aachen, Inst Tech & Macromol Chem, D-52074 Aachen, Germany
[2] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
[3] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[4] Univ Jena, Inst Anorgan & Analyt Chem, D-07745 Jena, Germany
关键词
chelates; dihydrogen complexes; hydrides; phosphine ligands; ruthenium; 16-ELECTRON DIHYDROGEN COMPLEXES; ZEROVALENT OLEFINIC DERIVATIVES; MOLECULAR-HYDROGEN COMPLEXES; RAY CRYSTAL-STRUCTURE; SP(3) C-H; PINCER COMPLEXES; BOND ACTIVATION; POLYHYDRIDE COMPLEXES; ELECTRONIC-STRUCTURE; NEUTRON STRUCTURE;
D O I
10.1002/chem.200600897
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and characterisation of nonclassical ruthenium hydride complexes containing bidentate PP and tridentate PCP and PNP pincer-type ligands are described. The mononuclear and dinuclear ruthenium complexes presented have been synthesised in moderate to high yields by the direct hydrogenation route (one-pot synthesis) or in a two-step procedure. In both cases [Ru(cod)(metallyl)(2)] served as a readily available precursor. The influences of the coordination geometry and the ligand framework on the structure, binding, and chemical properties of the M-H, fragments were studied by X-ray crystal structure analysis, spectroscopic methods, and reactivity towards N-2, D-2, and deuterated solvents.
引用
收藏
页码:1539 / 1546
页数:8
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