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Synthesis and structure of FeRu3(CO)13(μ-PPh2)2; A “64-electron” cluster complex with a planar triangulated rhomboidal array of metal atoms
Authors:Melvyn Rowen Churchill  Clifford Bueno  David A Young
Institution:Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14214 U.S.A;Research laboratories, Tennessee Eastman Co., Division of Eastman Kodak Co., Kingsport, Tennessee 37662 U.S.A.
Abstract:The species FeRu3(CO)13(μ-PPH2)2, synthesized from Ru3(CO)12 and Fe(CO)4(Ph2PPPh2),has been characterized both spectroscopically and via a single-crystal X-ray structural analysis. This complex crystallizes in the centrosymmetric triclinic space group P1 No. 2, Ci1] with a  10.066(3), b  12.899(3), c  17.003(4) Å, α  111.89(2), β  91.02(2), γ  102.00(2)°, V  1992.7(9) Å3, Z  2, ?(obsd)  1.79(2) g cm-3 and ?(calcd)  1.82 cm-3. Diffraction data were collected with a Syntex P21 automated four-circle diffractometer and the structure was refined to RF  6.0% and RWF  3.6% for all 5213 reflections (RF  3.8%, RWF  3.6% for those 4140 reflections with |Fo|> 3σ(|Fo|).The metal atoms define a planar triangulated rhombus, with atoms Ru(1) and Ru(2) at the bridgehead, and Fe(1) and Ru(3) at the acute apices. Fe(1) is linked to four terminal carbonyl ligands and is associated with the heteronuclear bonds Fe(1)Ru(1)  2.861(1) Å and Fe(1)Ru(2)  2.868(1) Å. The ruthenium atoms are each bonded to three terminal carbonyl groups. The retheniumruthenium distances are Ru(1)Ru(2)  3.098(1), Ru(1)Ru(3)  3.147(1), and Ru(2)Ru(3)  3.171(1) Å. The structure is completed by Ph2P bridges across the Ru(1)Ru(3) and Ru(2)(ru(3) vectors (<Ru(1)P(1)Ru(3)  84.89(5)° and <Ru(2)P(2)Ru(3)  85.56(6)°).
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