New Insights on the Mechanism of Palladium-Catalyzed Hydrolysis of Sodium Borohydride from 11B NMR Measurements

• Published in: The journal of physical chemistry. B Vol. 110; no. 34; pp. 17024 - 17033
• Main Authors: Guella, G, Zanchetta, C, Patton, B, Miotello, A
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 31.08.2006
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp063362n

To gain insight on the mechanistic aspects of the palladium-catalyzed hydrolysis of NaBH4 in alkaline media, the kinetics of the reaction has been investigated by 11B NMR (nuclear magnetic resonance) measurements taken at different times during the reaction course. Working with BH4 - concentration in the range 0.05−0.1 M and with a [substrate]/[catalyst] molar ratio of 0.03−0.11, hydrolysis has been found to follow a first-order kinetic dependence from concentration of both the substrate and the catalyst (Pd/C 10 wt %). We followed the reaction of NaBH4 and its perdeuterated analogue NaBD4 in H2O, in D2O and H2O/D2O mixtures. When the process was carried out in D2O, deuterium incorporation in BH4 - afforded BH4 - n D n - (n = 1, 2, 3, 4) species, and a competition between hydrolysis and hydrogen/deuterium exchange processes was observed. By fitting the kinetics NMR data by nonlinear least-squares regression techniques, the rate constants of the elementary steps involved in the palladium-catalyzed borohydride hydrolysis have been evaluated. Such a regression analysis was performed on a reaction scheme wherein the starting reactant BH4 - is allowed both to reversibly exchange hydrogen with deuterium atoms of D2O and to irreversibly hydrolyze into borohydroxy species B(OD)4 -. In contrast to acid-catalyzed hydrolysis of sodium borohydride, our results indicate that in the palladium-catalyzed process the rate constants of the exchange processes are higher than those of the corresponding hydrolysis reactions.