Syntheses of neutral halide and aryl vanadium bisimides are described. Treatment of VCl2(NtBu)[NTMS-((NBu)-Bu-t)], 2, with PMe3, PEt3, PMe2Ph, or pyridine gave vanadium bisimides via TMSC1 elimination in good yield: VCl(PMe3)(2)((NBu)-Bu-t)(2) 3, VCl(PEt3)(2)(NlBu)(2) 4, VCl(PMe2Ph)(2)((NBu)-Bu-t)(2) 5, and VCl(Py)(2)((NBu)-Bu-t)(2) 6. The halide series (Cl-I) was synthesized by use of TMSBr and TMSI to give VBr(PMe3)(2)((NBu)-Bu-t)(2) 7 and VI(PMe3)(2)((NBu)-Bu-t)(2) 8. The phenyl derivative was obtained by reaction of 3 with MgPh2 to give VPh(PMe3)(2)((NBu)-Bu-t)(2) 9. These neutral complexes are compared to the previously reported cationic bisimides [V(PMe3)(3)((NBu)-Bu-t)(2)][Al(PFTB)(4)] 10, [V(PEt3)(2)((NBu)-Bu-t)(2)][Al(PFTB)(4)] 11, and [V(DMAP)(PEt3)(2)((NBu)-Bu-t)(2)][Al(PFTB)(4)] 12 (DMAP = dimethylaminopyridine, PFTB = perfluoro-tert-butoxide). Characterization of the complexes by X-ray diffraction, C-13 NMR, V-51 NMR, and V L-3,L-2-edge X-ray absorption nearedge structure (XANES) spectroscopy provides a description of the electronic structure in comparison to group 6 bisimides and the bent metallocene analogues. The electronic structure is dominated by pi bonding to the imides, and localization of electron density at the nitrogen atoms of the imides is dictated by the cone angle and donating ability of the axial neutral supporting ligands. This phenomenon is clearly seen in the sensitivity of V-51 NMR shift, C-13 NMR Delta delta(alpha beta), and L-3-edge energy to the nature of the supporting phosphine ligand, which defines the parameters for designing cationic group 5 bisimides that would be capable of breaking stronger sigma bonds. Conversely, all three methods show little dependence on the variable equatorial halide ligand. Furthermore, this analysis allows for quantification of the electronic differences between vanadium bisimides and the structurally analogous mixed Cp/imide system CpV((NBu)-Bu-t)X-2 (Cp = C5H51-).