Jv. Barkley et al., COORDINATION OF HYDRAZINE AND SUBSTITUTED HYDRAZINES ON REACTION WITH[RH-2(CO)(4)CL-2] AND DISPROPORTIONATION OF 1,2-N2H2PH2, Journal of the Chemical Society. Dalton transactions, (4), 1998, pp. 697-701
The progressive addition of hydrazine and the following increasingly s
ubstituted hydrazines L (N2H4 Ia, H2NNHMe Ib, H2NNHPh Ie, H2NNMe2 Id,
or MeHNNHMe Ic) to [Rh-2(CO)(4)Cl-2] resulted in the initial formation
of [{Rh(CO)(2)Cl}(2)(mu-L)] 1 followed by the formation of cis-[Rh(CO
)(2)L(Cl)] 2; analogous mononuclear complexes were formed directly on
addition of the more heavily substituted hydrazines Me2NNMe, IIf and H
2NNPh2 IIg, but addition of 1,2-N2H2Ph2 IIIh to [Rh-2(CO)(4)Cl-2] resu
lted in disproportionation of the hydrazine and formation of cis-[Rh(C
O)(2)(NH2Ph)Cl] 3 and cis-[Rh(CO)(2)(PhN=NPh)Cl] 4. The above complexe
s have been spectroscopically characterised by IR and C-13/N-15 NMR me
asurements. X-Ray structural analysis on [{Rh(CO)(2)Cl}(2)(mu-L)] (L =
H2NNHMe or MeHNNHMe) confirmed that L adopts mu-eta(1):eta(1)-mode of
bonding with a cisoid arrangement of the Rh(CO)(2)Cl groups about the
N-N bond.