Hemilabile ligands

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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

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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Supported Organometallic Complexes Part 39: Cationic Diamine(Ether–Phosphine)Ruthenium(II) Complexes as Precursors for the Hydrogenation of Trans-4-Phenyl-3-Butene-2-One

Journal Title, Volume, Page: 
Inorganica Chimica Acta Volume 357, Issue 6, 20 April 2004, Pages 1847–1853 Protagonists in Chemistry: Helmut Werner
Year of Publication: 
2004
Authors: 
Ismail Warad
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tubingen, 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 Tubingen, Germany
Hermann A Mayer
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tubingen, Germany
Ekkehard Lindner
Institut für Anorganische Chemie der Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tubingen, Germany
Current Affiliation: 
Preferred Abstract (Original): 
Treatment of RuCl2(η1-Ph2PCH2CH2OCH3)2(diamine) (1L1–1L7) with one equivalent of AgX (X=OTf, BF4) in CH2Cl2 results in the formation of the monocationic ruthenium(II) complexes [RuCl(η1-Ph2PCH2CH2OCH3)(η2-Ph2PCH2CH2OCH3)(diamine)]+X− (2L1–2L7). These complexes were characterized by NMR, and mass spectroscopy as well as by elemental analyses, 2L1 additionally by an X-ray structural analysis. Complex 2L1 crystallizes in the monoclinic space group C2/c with Z=8. The monocationic and neutral complexes were applied as catalysts in the selective hydrogenation of trans-4-phenyl-3-butene-2-one. With the exception of 1L3/1L7 and 2L3/2L7 all catalysts showed high activities and selectivities toward the hydrogenation of the carbonyl group under mild conditions. However, the activity of the cationic catalysts is only half of that of their neutral congeners.
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