Supported Organometallic Complexes Part 34: Synthesis and Structures of An Array of Diamine(Ether–Phosphine)Ruthenium(II) Complexes and Their Application In The Catalytic Hydrogenation of Trans-4-Phenyl-3-Butene-2-One

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Journal Title, Volume, Page: 
Inorganica Chimica Acta Volume 350, 4 July 2003, Pages 49–56
Year of Publication: 
2003
Authors: 
Ekkehard Lindner
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany
Ismail Warad
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany
Current Affiliation: 
Department of Chemistry, Faculty of Science, An-Najah National University, Nablus, Palestine
Klaus Eichele
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany
Hermann A Mayer
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany
Preferred Abstract (Original): 
The novel diamine–bis(ether–phosphine)ruthenium(II) complexes Cl2Ru(η1-Ph2PCH2 CH2OCH3)2(diamine)2(3L1–3L11) have been obtained by reaction of equimolar amounts of Cl2Ru(P∩O)2 (2) with the respective diamines L1–L11 in good yields. X-ray structural investigations of 3L2 and 3L8 show monoclinic unit cells with the space group P21/c. The octahedrally coordinated ruthenium atoms have each two trans-chlorides and cis-phosphines which is in agreement with NMR studies in solution. With the exception of 3L4 all mentioned ruthenium complexes are highly catalytically active in the hydrogenation of the α,β-unsaturated ketone trans-4-phenyl-3-butene-2-one. In most cases the conversions and selectivities toward the formation of the unsaturated alcohol trans-4-phenyl-3-butene-2-ol were 100% with high turnover frequencies under mild conditions. Novel diamine–bis(ether–phosphine)ruthenium(II) complexes have been prepared and characterized. X-ray structural investigations of 3L2 and 3L8 show monoclinic unit cells with the space group P21/c. These complexes are highly catalytically active in the hydrogenation of an α,β-unsaturated ketone, with excellent conversions and selectivities under mild conditions.
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