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Issue 1, 1983
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Multinuclear magnetic resonance studies on [Rh4(CO)12–xLx][L = P(OPh)3, x= 1–4]

Abstract

Direct 103Rh n.m.r. studies on [Rh4(CO)12–xLx][L = P(OPh)3, x= 1–4] at low temperatures support the solution structures previously proposed and, although the apical rhodium resonance always occurs at lowest frequency, there is little variation in δ(103Rh) with increasing ligand substitution. Measurements of 13C-{103Rh} allow unambiguous assignment of the 13C n.m.r. spectra when x= 1 and 3 and δ(13COax) is always at lowest frequency with 1J(103Rh–13COax)≃1J(103Rh–13COap) < 1J(103Rh–13COrad); this suggests a new assignment for the 13C n.m.r. spectrum of [Rh4(CO)12].

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Article type: Paper
DOI: 10.1039/DT9830000173
Citation: J. Chem. Soc., Dalton Trans., 1983,0, 173-175
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    Multinuclear magnetic resonance studies on [Rh4(CO)12–xLx][L = P(OPh)3, x= 1–4]

    B. T. Heaton, L. Strona, R. D. Pergola, L. Garlaschelli, U. Sartorelli and I. H. Sadler, J. Chem. Soc., Dalton Trans., 1983, 0, 173
    DOI: 10.1039/DT9830000173

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