A new kind of nonmetallic
atom-doped boron cluster is described
herein theoretically. When a phosphorus atom is added to the B12 motif and loses an electron, a novel B12 cage
is obtained, composed of two B3 rings at both ends and
one B6 ring in the middle, forming a triangular bifrustum.
Interestingly, this B12 cage is formed by three B7 units joined together from three directions at an angle of 120°.
When two P atoms are added to the B12 motif, this novel
B12 cage is also obtained, and two P atoms are attached
to the B3 rings at both ends of the triangular bifrustum,
forming a triangular bipyramid (Johnson solid). Amazingly, the global
minimums of neutral, monocationic, and monoanionic P2B12+/0/– have the same cage structure with
a D3h symmetry; this
is the smallest boron cage with the same structure. The P atom has
five valence electrons, according to adaptive natural density partitioning
bonding analyses of cage PB12+ and P2B12, in addition to one lone pair, the other three electrons
of the P atom combine with an electron of each B atom on the B3 ring to form three 2c–2e σ bonds and form three
electron sharing bonds with B atoms through covalent interactions,
stabilizing the B12 cage. The calculated photoelectron
spectra can be compared with future experimental values and provide
a theoretical basis for the identification and confirmation of PnB12– (n = 1–2)