Synthesis of Bis(germacyclopropa)benzenes and Structures of Their Annelated Benzene Rings

Extremely hindered bis(germacyclopropa)benzenes (3a,b; the IUPAC name is 4,8-digermatricyclo[5.1.0.03,5]octa-1,3(5),6-triene) were synthesized as stable crystalline compounds by the reaction of the
corresponding dilithiogermane Tbt(Dip)GeLi2 (8; Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl, Dip
= 2,6-diisopropylphenyl) with 1,2,4,5-tetrabromobenzene. The structures of the two stereoisomeric bis(germacyclopropa)benzenes (3a, cis isomer; 3b, trans isomer) were definitively determined by X-ray
crystallographic analysis. The central benzene ring of 3a was found to be folded, in contrast to the planar
benzene ring of 3b. The X-ray crystallographic analyses of 3a and 3b and the theoretical calculations for
some model molecules revealed that the annelated benzene rings have no distinct bond alternation.