Cleavage of 9-iodo-1,7-carborane with potassium hydroxide in butanol, involving substitution of the iodine atom by a butoxy group and yielding 1-butoxy- and 5-butoxy-nido-7,9-dicarbaundecaborate anions
Li. Zakharkin et al., Cleavage of 9-iodo-1,7-carborane with potassium hydroxide in butanol, involving substitution of the iodine atom by a butoxy group and yielding 1-butoxy- and 5-butoxy-nido-7,9-dicarbaundecaborate anions, RUSS J G CH, 70(1), 2000, pp. 71-72
When heated in butanolic KOH, 9-iodo-1,7-carborane cleaves to stereoisomeri
c nido-7,9-di-carbaundecaborate anions. The latter exchange under the react
ion conditions their iodine atom for a butoxy group to give 1-butoxy- and 5
-butoxy-nido-7,9-dicarbaundecaborate anions.