Crystallization of colourless hexanitratoneptunate(IV) with anhydrous H+ countercations trapped in a hydrogen bonded polymer with diamide linkers

Colourless crystalline compounds of centrosymmetric [Np(NO3)(6)](2-) were yielded from 3 M HNO3 aq in the presence of double-headed 2-pyrrolidone derivatives (L). In the obtained crystal structures, H+ was also involved as a countercation to compensate for the negative charge of [Np(NO3)(6)](2-), where the initial hydration around H+ was fully removed during crystallization despite it having the strongest hydration enthalpy. Instead, this anhydrous H+ was captured by L to form a [H+MIDLINE HORIZONTAL ELLIPSISL](n) hydrogen bonded polymer. In [Np(NO3)(6)](2-), the Np4+ centre is twelve-coordinated with 6 bidentate NO3-, and therefore, present in an icosahedral geometry bearing inversion centre. In such a centrosymmetric system, any f-f transitions stemming from the 5f(3) electronic configuration of Np4+ are electric-dipole forbidden. This is the reason why the compounds currently obtained were colourless unlike ordinary Np(iv) species, which are olive-green.