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Cp*MoH[sub 5](PMe[sub 3]). A classical polyhydride with a pentagonal-bipyramidal structure and a long T[sub 1] relaxation time

Journal Article · · Organometallics; (United States)
DOI:https://doi.org/10.1021/om00030a060· OSTI ID:6297766
; ;  [1]
  1. Univ. of Maryland, College Park (United States)
Cp*MoH[sub 5](PMe[sub 3]) has been prepared from Cp*MoCl[sub 2](PMe[sub 3]) and LiAlH[sub 4]. The compound is analogous to the previously reported Cp*WH[sub 5](PMe[sub 3]) and CpWH[sub 5](PMe[sub 3]) (Green, M.L.H.; Parkin, G.J. Chem. Soc., Chem. Commun. 1984, 1467. Schrock, R. R.; et al. Organometallics 1986, 5, 1681) for which structural assignments were not made. A single sharp [sup 1]H-NMR resonance is observed for the five hydrides down to 183 K, consistent with either a static symmetric structure or a highly fluxional structure, either classical or nonclassical. The measured minimum longtudinal relaxation time, T[sub 1], is quite long (780 ms at 400 MHz and 230 K) and consistent with a classical structure based on the pentagonal bipyramid which gives rise to a substantially anisotropic moment of inertia. 14 refs., 1 tab.
OSTI ID:
6297766
Journal Information:
Organometallics; (United States), Journal Name: Organometallics; (United States) Vol. 12:6; ISSN ORGND7; ISSN 0276-7333
Country of Publication:
United States
Language:
English