RESUMEN
The reaction of hydrazinium sulfate and chlorosulfonic acid in pyridine leads to the pyridinium salt of the hydrazine disulfonate anion, [(SO3)HNNH(SO3)]2-. The salt is the starting material for the preparation of further hydrazine disulfonates, for example of alkaline metals and barium. In all compounds, the [(SO3)HNNH(SO3)]2- anion adopts the gauche conformation. The conformer is chiral but all of the investigated compounds crystallize as racemates. The disulfonate anion can occur in another constitution with the two sulfonate groups attached to only one nitrogen atom. This so-called hydrazine iso-disulfonate, [H2NN(SO3)2]2-, has been prepared through a substitution reaction between potassium imidodisulfonate, K[HN(SO3)2], and hydroxylamine-O-sulfonic acid, H2NOSO3H. The hydrazine iso-disulfonate anion has been crystallized as potassium and barium compound, respectively. The compounds were characterized by XRD, vibrational spectroscopy, DFT calculations and thermal analyses.
RESUMEN
The reaction of hydrazine hydrate, N2 H4 â H2 O, and SO3 leads to hydrazine sulfonic acid (Pca21 , a=849.59(4)â pm, b=482.18(2)â pm, c=832.17(4)â pm). Structure elucidation reveals the zwitter-anionic nature of the compound according to NH3 NH(SO3 ). With the barium salt Ba[NH2 NH(SO3 )]2 (H2 O), a first salt of hydrazine sulfonic acid has been prepared (P 1 â¾ $\bar 1$ , a=489.75(5)â pm, b=737.52(7)â pm, c=1317.4(1)â pm, α=88.238(4)°, ß=84.761(4)°, γ=79.701(4)°). The compounds were characterized by vibrational spectroscopy, DFT calculations and thermal analyses.
RESUMEN
The reaction of hexachlorophosphazene, P3 N3 Cl6 , with SO3 and the gold halides AuCl3 and AuBr3 , respectively, leads to the new cyclic anionic tetramer, [S4 N2 O10 ]2- , which is coordinated to Au3+ in the dimeric complexes [Au2 X2 (S4 N2 O10 )2 ] (X=Cl, Br). The [S4 N2 O10 ]2- anion can be seen as the condensation product of two sulfate anions, [SO4 ]2- , and two amidosulfate anions, [NH2 SO3 ]- .