Abstract

The thermal decomposition of borine carbonyl has been carried out in the presence of triethylamine, a very suitable scavenger of borine (BH3). The bimolecular reaction does not compete with the unimolecular rupture of the B–C bond. At 0°, the pressure-dependence of the unimolecular rupture has been studied, kunimol being equal to ½k∞ at 90 torr when propane is used as third body. From the value of k∞, and assuming a value of 1013·4 sec.–1 for the pre-exponential factor A, the activation energy is Ea= 21·4 ± 1·2 kcal./mole. The dissociation energy of the B–B bond in diborane is then calculated to be D(B–B)= 33·5 ± 2·4 kcal./mole, if the recombination reaction of borine and carbon monoxide has Ea= 0.

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