The reduction of 6,12-dichloro-1,2,3,4,7,8,9,10-octahydro-6H,12H-[1,2,3]benzodiazaphospholo [2,1-a] [1,2,3]benzodiazaphosphole (3) by metallic magnesium in tetrahydrofuran (THF) affords the N,N'-fused bisphosphole 1 in 92% yield. The compound reveals a novel type of 10 pi-electron heteroaromatic system [NICS(0) = -11.4], containing a two-coordinate and formally divalent phosphorus atom. Compound 1 possesses a much higher coordination activity than many other diazaphospholes. This is caused by a novel type of complexation to a metal ion wherein the lone phosphorus pairs are not involved in metal coordination. Instead, the 10 pi-electron heteroaromatic system provides two electrons for P -> M bond formation. Polarization of the ligand results in the formation of extended molecular associates or cluster compounds. Complexes of 1 with mercury dichloride [{(1)(3)HgCl}(2)(mu(6)-Cl)]Cl-+(-) (7) and tin dichlorides [1 center dot SnCl2(PhMe solvate)] (8a) and [1 center dot SnCl2] (8b) are, in fact, supramolecular in nature, containing multiple intermolecular short contacts. Crystals of complex 8a containing short Sn center dot center dot center dot Sn packing interactions were converted reversibly to metallic tin after workup with THF. The simple mixing of 1 and 3 (1:1) gave a P-P bridging dimeric species prone to easy dissociation. The addition of GeCl2(diox) to the equimolar mixture of 1 and 3 shifted the equilibrium to the formation of a poorly soluble salt-like dimer 6, which is, in fact, a stacked 18 pi-electron dication having a through-space delocalization of pi electrons.