The [(Bu4N)-Bu-n][AuX2(CN)(2)] (X = Br, I) salts were synthesized and structurally characterized. Both feature square-planar [AuX2(CN)(2)] anions, with trans cyano and halo ligands, which aggregate via halogen-halogen interactions. The aggregation of [AuX2(CN)(2)] units results in the parallel alignment of all of the Br-Au-Br moieties in the anions along the [110] and [1 (1) over bar0] directions. Two crystal habits of [(Bu4N)-Bu-n][AuBr2(CN)(2)] were grown: with (1 (1) over bar0) and (001) as the primary faces. The birefringence in the (1 (1) over bar0) plane was found to be Delta n = 0.051(4) and was <0.03 in the (001) plane. Using the [AuBr2(CN)(2)](-) unit, [M(phen)(2)][AuBr2(CN)(2)](2) (M = Fe, Ni), [Ni(terpy)(2)][AuBr2(CN)(2)](2), [Fe(terpy)(2)]-[AuBr2(CN)(2)][ClO4], and [Cu(phen)(2)(NO3)][AuBr2(CN)(2)] (phen = 1,10-phenanthroline, terpy = 2,2';6',2 ''-terpyridine) were synthesized and structurally characterized: they formed ionic structures with coordinatively saturated metal cations and structurally aligning Br center dot center dot center dot Br interactions between the [AuBr2(CN)(2)](-) anions. A molecular complex, Cu(terpy)[AuBr2(CN)(2)](2), was prepared, as well as the coordination polymer, [Ni(en)(2)(AuBr2(CN)(2))][AuBr2(CN)(2)] center dot MeOH (en = ethylenediamine). The structure consists of layers of chains of Ni(en)(2)(AuBr2(CN)(2))(+) units and chains of unbound [AuBr2(CN)(2)] units formed via Br center dot center dot center dot Br interactions; a Delta n = 0.131(3) was measured. The An values were related to the supramolecular structures in terms of the relative intermolecular alignment of Br-Au-Br and NC-Au-CN bonds. These measurements both demonstrate the utility of the Au-Br bonds in enhancing birefringence and show that the contribution of the M-CN units to the overall birefringence of cyanometallate coordinations polymers is non-negligible.