
%0 Journal Article
%A Batts, BD 
%A Spinner, E 
%T Spectral and structural studies of 4-aminopyridines substituted at the 4-nitrogen atom. 4-Nitraminopyridine, 4-hydrazinopyridine, and theirions
%J Australian Journal of Chemistry
%D 1969/12/01
%V 22
%N 12
%P 2611-2626
%K 
%R https://doi.org/10.1071/CH9692611
%U https://www.publish.csiro.au/paper/CH9692611 
%X Ultraviolet, infrared, and nuclear magnetic resonance spectra, and ionization constants, have been determined for 4-nitraminopyridine, 4- (methylnitramino)-pyridine, 1,4-dihydro-1-methyl-4-nitriminopyridine, 4-hydrazinopyridine, 1,4-dihydro-1-methylpyridin-4-one hydrazone, and their ions. 4-Nitraminopyridine exists in the nitrimine tautomeric form (II) in the solid state, in water (in c. 99%), ethanol, dimethyl sulphoxide, and acetonitrile, but in dioxan it is mostly (c. 94%) in the nitramino form (I). 4-Hydrazinopyridine exists predominantly in the hydrazine form.     Infrared spectra characteristic of pyridinium ions are shown by the cation of 4-nitraminopyridine (X) and the dication of 4- hydrazinopyridine (XIV); in both the ring nitrogen carries a positive charge. The infrared spectrum of the monocation of 4-hydrazinopyridine is not that of a pyridinium ion, and shows 4-pyridonoid features; the positive charge resides essentially on the 4-nitrogen atom (XIII), as in the unsubstituted 4-aminopyridine cation.     Cation formation moves the a- and &#946;-proton magnetic resonances of both 4-(methylnitramino)pyridine and 1,4-dihydro-1-methyl-4- nitriminopyridine to substantially lower 7 values. Monocation formation reduces the T value of the &#946;-proton resonance of 4-hydrazinopyridine by a relatively small amount, and changes that of the a-proton only slightly (upward). Formation of the dication of 4-hydrazino-pyridine (XIV) lowers both T values substantially. 
