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A full kinetic analysis of the platinum catalyzed hydrolysis of sodium borohydride (NaBH 4 ) in alkaline media has been performed using 11 B NMR (nuclear magnetic resonance) spectroscopy with a Pt/C 5 wt % commercial powder as catalyst. By fitting the NMR data by least-square regression techniques, the rate constants of platinum catalyzed borohydride hydrolysis have been evaluated. Within the investigated [borohydride]/[catalyst] molar ratio of 200−1500, the rate law has been found to be of first-order in catalyst and zero order in borohydride. Whereas no reagent-isotope kinetic effect is observed in the NaBD 4 /H 2 O reaction system, the hydrolysis of NaBH 4 in deuterated water shows a significant solvent-kinetic isotope effect. In both cases, however, 11 B NMR analysis indicates that the main reaction product is the tetrahydroxyborate species (D) n H 4- n BO 4 - ( n = 1, 2, 3, 4) followed by a minor amount of the partially scrambled BH 3 D - species while the hydrolysis-intermediates H n B(OD) 4- n - ( n = 1, 2, 3) species are not detectable during all the reaction time. These results suggest that, differently from the Pd catalyzed/borohydride(borodeuteride) hydrolytic process, the hydrogen/deuterium exchange is slower than hydrolysis and that the rate-determining step of the overall process is the formation of the monohydroxy-borohydride intermediate BH 3 OH - . The activation energy of the overall process has been also evaluated by 11 B NMR rate measurements taken at different temperatures.
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Guella et al. (2007) studied this question.
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