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    Synthesis and properties of tetra-μ-acetatodiruthenium(II,III) phenylphosphinate and phenylphosphonate complexes: X-ray crystal structures of [Ru2(μ-O2CCH3)4(HPhPO2)2]H and [Ru2(μ-O2CCH3)4(PhPO3H)2]H·H2O


    McCann, Malachy and Murphy, Eamonn and Cardin, Christine and Convery, Maire (1993) Synthesis and properties of tetra-μ-acetatodiruthenium(II,III) phenylphosphinate and phenylphosphonate complexes: X-ray crystal structures of [Ru2(μ-O2CCH3)4(HPhPO2)2]H and [Ru2(μ-O2CCH3)4(PhPO3H)2]H·H2O. Polyhedron, 12 (14). pp. 1725-1731. ISSN 0277-5387

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    Abstract

    Phenylphosphinic acid (HPhPO2H) and phenylphosphonic acid (PhPO3H2) react with a methanolic solution of [Rui(µ-O2CCH3MO2CCH3h]H · 0.7H2O at room tempera­ture to give [Rui(µ-O2CCH3MHPhPO2) 2]H (1) and [Ruiµ-O2CCH3)4 (PhPO3H)2]H · H2O (2), respectively. The X-ray crystal structures of 1 and 2 each show the Ru-Ru core to be ligated by four bridging bidentate acetate ligands [Ru-Ru distances: 1 = 2.272( I) A; 2 = 2.267(2) A.) and two axial phenylphosphinate and phenylphosphonate ligands, respec­tively. In each complex the individual bimetallic molecules are linked together by a hydrogen ion which bridges the oxygen atoms of neighbouring axial ligands. In 2 the water molecule is also hydrogen-bonded to one of the axial phenylphosphonate groups. Spectroscopic, magnetic and cyclic voltammetric data for the complexes are given.

    Item Type: Article
    Keywords: Synthesis; properties;tetra-μ-acetatodiruthenium(II,III); phenylphosphinate; phenylphosphonate complexes; X-ray; crystal; structures; [Ru2(μ-O2CCH3)4(HPhPO2)2]H; [Ru2(μ-O2CCH3)4(PhPO3H)2]H·H2O;
    Academic Unit: Faculty of Science and Engineering > Chemistry
    Item ID: 14561
    Identification Number: https://doi.org/10.1016/S0277-5387(00)84604-5
    Depositing User: Dr. Malachy McCann
    Date Deposited: 23 Jun 2021 14:27
    Journal or Publication Title: Polyhedron
    Publisher: Elsevier
    Refereed: Yes
    URI:
      Use Licence: This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here

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