“…As expected from the involvement of the electron lone pair in the chemical bond formation, the SbÀ N distances in Sb 3 N 5 , ranging from 1.97 to 2.21 Å (Table SI-1), are consistent with the available experimental and calculated literature data at ambient pressure (section SI-3), with the single bond length values estimated from the sum of the calculated covalent radii of Sb and N (~2.1 Å) at ambient pressure [48] and with recently synthesized SbCN 3 at high pressure (2.0179 Å at 32.7 GPa, 2.022 Å at 32.8 GPa). [34] The SbÀ N bond lengths in Sb 3 N 5 are also in agreement with the SbÀ N bond lengths of the antimony nitride crystalline structures calculated by Lian et al [33] However, SbÀ N distances ranging between 2.35 and 2.56 Å at ambient pressure, comparable to our Sb02-N03 distances of 2.54 Å at 35 GPa, have been reported in the (PNP) 2 [Sb(pc 2À ) 2 ]Br•2 Et 2 O complex of Sb(V) (PNP = triphenylphosphine, pc = phthalocyaninate), where Sb exhibits square antiprismatic coordination by eight N atoms, four of which are located on one of two crown ether like chelating rings and four on the other. [49] Considering a cutoff SbÀ N single-bond length of 2.50 Å, well beyond the longest experimentally reported SbÀ N single bond length of 2.324(2) at ambient pressure ([Sb-(N 3 ) 5 ] 2À ) [45] in non-chelating ligands, and thus excluding the two Sb02-N03 distances of 2.54 Å (Table SI-1), the crystalline structure of Sb 3 N 5 can be described in terms of polyhedra as made of octahedral and trigonal prismatic SbN 6 units, respectively involving the Sb01 and Sb02 atoms, of NSb 4 distorted tetrahedra, respectively involving the N01 and N02 atoms, and of NSb 3 trigonal pyramids, involving the N03 atoms, which are illustrated in Figure 3 (panels A, B, C, G, H, I, L, M and N).…”