The aluminum and gallium dichlorides (Mamx)ECl2 la (E = Al; 82%) and 1b (E = Go; 79%) (Mamx = 2,4-ditert-butyl-6-[(dimethylamino)methyl]phenyl) reacted with dilithioferrocene or dilithioruthenocene to give [1]ferrocenophanes (2a, 2b) and [1]ruthenocenophanes (3a, 3b), respectively. The galla[1]ruthenocenophane 3b could be isolated from the reaction mixture through precipitation into hexane (50%), while 2a, 2b, and 3a underwent ring-opening polymerization under the reaction conditions of their formation reactions to give metallopolymers (M-w (DLS) between 8.07 and 106 kDa). Monomer 3b was polymerized using Karstedt's catalyst resulting in an M-w of 28.6(+/- 6.3) kDa. In order to get an indication of the structure of polymers, bis(ferrocenyl) compounds (Mamx)EFc(2) (E = Al (4a), 51%; E = Ga (4b), 49%) were prepared and characterized by single crystal X-ray analysis. DFT calculations shed some light on the unexpected high reactivity of these new strained sandwich species. Optimized geometries of known aluminum and gallium-bridged [1]ferrocenophanes (Al(Pytsi) (6a), Ga(Pytsi) (6b); Pytsi = [dimethyl(2-pyridyl)silyl]bis(trimethylsilyl)methyl) and [1]ruthenocenophanes (Al(Me(2)Ntsi) (7a), Ga(Me(2)Ntsi) (7b); Me(2)Ntsi = [(dimethylamino)dimethylsilyl]bis(trimethylsilyl)methyl) matched very well with experimental molecular structures. Geometries of species 2a, 2b, 3a, and 3b were optimized (BP86/TZ2P) and the structural influence of the tBu group of the Mamx ligand in ortho position was evaluated by optimizing molecular structures of the four unknown species where the ortho-tBu group was replaced by an H atom (2a(H), 2b(H), 3a(H), and 3b(H)). The most pronounced structural effect was seen as a change of the orientation of the bridging moiety with respect to the sandwich unit. As the tBu group was removed, the aromatic ligand moved toward the freed-up space. The energetics (Delta E, Delta H-298K, and Delta G(298)K) accompanied by the structural changes were evaluated by a hydrogenolysis reaction of strained species resulting in Cp2M (M = Fe, Ru) and respective aluminum and gallium dihydrides. This nonisodesmic reaction showed that [1]metallocenophanes equipped with the ortho-tBu group were on average 5.5 kcal/mol higher strained (Delta H-298K) than species where the tBu group was lacking. The investigation of the isodesmic reaction between strained species and Cp2M yielding bis(metallocenyl) compounds revealed that the ortho-tBu group sterically interacts with one of the metallocenyl units. The bis(metallocenyl) compounds are model compounds for the respective metallopolymers and one can conclude that even though the ortho-tBu group imposes additional strain on the starting metallocenophanes, this effect cancels out in ROPs because the ortho-tBu group imposes a similar strain on the resulting polymers. The uncovered steric repulsion between the ortho-tBu group and the sandwich moieties probably causes the ortho-tBu to act as an unusually sensitive NMR probe of the tacticity of the polymers.