
Journal of the Chemical Society, Dalton Transactions p. 277 - 290 (1983)
Update date:2022-08-11
Topics:
Johnson, Brian F. G.
Lewis, Jack
Nicholls, J. Nicola
Puga, Jose
Raithby, Paul R.
Rosales, Maria J.
The hexaruthenium cluster a = 16.448(3), b = 14.274(2), c = 20.834(4) Angstroem, β = 91.36(2) deg, and Z = 8.The structure was found to be isomorphous with the analogue a square-pyramidal geometry with an exposed carbido-atom lying 0.11(2) Angstroem beneath the basal plane.Reaction of complex (1) with the nitrogen-donor ligand MeCN yields the adduct a bridged butterfly arrangement of metal atoms with a central carbido-atom.The complex crystallises in space group P21/n with a = 14.116(6), b = 18.167(7), c = 10.276(4) Angstroem, β = 95.14(3) deg, and Z = 4; the structure was solved by direct methods and difference techniques and refined to R = 0.047 for 1 604 diffractometer data.Reactions of complex (1) with tertiary phosphine ligands PR3 a = 9.953(2), b = 12.247(2), c = 14.703(3) Angstroem, β = 91.23(2) deg, and Z = 2, (3b) in space group P21/c with a = 15.923(4), b = 12.494(3), c = 25.210(7) Angstroem, β = 93.28(2) deg, and Z = 4.Both structures were solved by a combination of direct methods and Fourier techniques and were refined to R = 0.021 for 3 305 reflections (3a) and R = 0.039 for 4 127 reflections (3b), respectively.Hydrogenation of (6) gives the dihydro-complex a = 12.210(4), b = 18.602(6), c = 18.409(6) Angstroem, β = 97.63(2) deg, and Z = 4.The structure was solved using the same techniques as the other complexes and refined to R = 0.064 for 3 510 diffractometer data.Treatment of complex (1) with halide ions gives the anionic clusters
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