I l l The Ir-bond orders calculated from the bond lengths according to established equations"2] are 1.00 for the C5-C6 bond. 0.34 for the C5--N3 bond, and 0.15 for the C&N4 bond. [12] G .
Electronic structure of two heterotrinuclear metal complexes [Ru2Co(μ3-O)(μ-CH3CO2)6L3](L=H2O, Py)
✍ Scribed by M. Velayutham; C.S. Gopinath; S. Subramanian
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 397 KB
- Volume
- 249
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Two 1~3-oxo carboxylate-bridged heterotrinuclear (ruthenium, cobalt) [Ru2Co(~3-O)(I.I,-CH3CO2)6L 3] (L = H20, Py) complexes have been prepared. EPR studies at 77 K show that there is no interaction between the ruthenium and cobalt ions. The ground state of high-spin cobalt is a spin doublet and the two ruthenium ions are antiferromagnetically coupled. IR data show two different types of acetate groups bridging the trinuclear system and the absence of threefold symmetry. ESCA results reveal that the central ix3-oxo bridge is highly covalent and there is no interaction between the ruthenium and cobalt ions.
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The reactions of [Pt3R~6(CO),l(p-H)3(p3-H)] (1) with PMe3 and PPh3 have produced the salts [Pt(PR3)3H]-[Pt3R~6(CO)2,(p3-H)(p-H)2]r 5a and 5d, R = Me and Ph in the yields 9% and 22%, respectively. By contrast the reaction of 1 with PPh, in the presence of Me3N0 has yielded the phosphane-substituted d
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