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M(diphosphine)22+ complexes (where M = Ni and Pt) react with hydrogen in the presence of bases to form the corresponding hydrides, HM(diphosphine)2+. In seven cases, equilibria have been observed from which the hydride donor ability (DeltaGdegrees(H-)) of the hydrides can be calculated. For six of these complexes, the DeltaGdegrees(H-) values calculated using heterolytic activation of hydrogen are compared with those based on thermodynamic cycles using pK(a) measurements and electrochemical half-wave potentials. The agreement between these two methods is good (within 1 kcal/mol). The reactivity of the various M(diphosphine)22+ complexes toward hydrogen parallels their measured hydride acceptor abilities.
Curtis et al. (Fri,) studied this question.
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