Coaxial Triple-Layered versus Helical Be6 B11- Clusters: Dual Structural Fluxionality and Multifold Aromaticity.
Jin-Chang GuoLin-Yan FengYing-Jin WangSaid JalifeAlejandro Vásquez-EspinalJosé Luis CabellosSudip PanGabriel MerinoHua-Jin ZhaiPublished in: Angewandte Chemie (International ed. in English) (2017)
Two low-lying structures are unveiled for the Be6 B11- nanocluster system that are virtually isoenergetic. The first, triple-layered cluster has a peripheral B11 ring as central layer, being sandwiched by two Be3 rings in a coaxial fashion, albeit with no discernible interlayer Be-Be bonding. The B11 ring revolves like a flexible chain even at room temperature, gliding freely around the Be6 prism. At elevated temperatures (1000 K), the Be6 core itself also rotates; that is, two Be3 rings undergo relative rotation or twisting with respect to each other. Bonding analyses suggest four-fold (π and σ) aromaticity, offering a dilute and fluxional electron cloud that lubricates the dynamics. The second, helix-type cluster contains a B11 helical skeleton encompassing a distorted Be6 prism. It is chiral and is the first nanosystem with a boron helix. Molecular dynamics also shows that at high temperature the helix cluster readily converts into the triple-layered one.