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This work reports, for the first time, the synthesis and structural characterization of both carbon-atoms-adjacent and carbon-atoms-apart 13-vertex carboranes and 14-vertex metallacarborane without C,C‘-linkages using direct and indirect methods. The results show that the C,C‘-linkages do not have any obvious effect on the thermal and kinetic stability of 13-vertex carboranes, and the CAp isomer is thermodynamically more stable than the CAd one. The role of the linkages is just to lower the reducing power of the nido -carborane dianions, facilitating the capitation reaction. CAp 13-vertex carboranes can be directly prepared by the reaction of [ nido -7,9-R 2 -7,9-C 2 B 10 H 10 ]Na 2 with dihaloborane reagents. However, the yield is rather low due to the very strong reducing power of the CAp nido -carborane dianions. This work supports our earlier argument that the prevention of the redox reactions is the key to obtaining successively larger carboranes.
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Zhang et al. (2006) studied this question.
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