Boron forms a rich variety of low-dimensional nanosystems, including the newly discovered helix Be6 B10 2- (1) and Be6 B11 - (2) clusters. We report herein on the elucidation of chemical bonding in clusters 1/2, using the modern quantum chemistry tools of canonical molecular orbital analyses and adaptive natural density partitioning (AdNDP). It is shown that clusters 1/2 contain a chiral helix Be2 B10 Be2 or Be2 B11 Be2 skeleton with a total of 11 and 12 segments, respectively, which effectively curve into "helical pseudo rings" and chemically consist of two "quasicircles" as defined by their anchoring Be centers. The helix skeleton is connected via Lewis-type B-B and Be-B-Be σ bonds, being further stabilized by island π/σ bonds and a loose π bond at the junction. The Be6 component in 1/2 assumes a distorted prism shape only physically, and it is fragmented into four parts: two terminal Be2 dimers and two isolated Be centers. A Be2 dimer at the far end manages to bend over and cap a quasicircle from one side of B plane. Consequently, each quasicircle of a helical pseudo ring is capped from opposite sides by two Be2 /Be units, facilitating intramolecular charge-transfers of 5 electrons from Be to B. Overall, the folding of B helix involves as many as 10 electrons. The enormous electrostatics offers the ultimate driving forces for B helix formation.
Keywords: boron-based helix clusters; chemical bonding.; chemical transmutation; electron-transfer complexes; formation mechanism.
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