Generation of nanopores during desorption of NH3 from Mg(NH3)6Cl2

It is shown that nanopores are formed during desorption of NH3 from Mg(NH3)6Cl2, which has been proposed as a hydrogen storage material. The system of nanopores facilitates the transport of desorbed ammonia away from the interior of large volumes of compacted storage material. DFT calculations show that there exists a continuous path from the initial Mg(NH3)6Cl2 material to MgCl2 that does not involve large-scale material transport. Accordingly, ammonia desorption from this system is facile.     

Bimetallic assemblies, [Ni(en)2]3[M(CN)6]2·3H2O (en = H2NCH2CH2NH2; M = Fe,Co)

The reaction between tris(ethyl­enedi­amine)­nickel(II) cations and hexa­cyanometallate(III) anions (M = Fe, Co) yields ordered bimetallic assemblies, catena‐poly­[[tris­(ethyl­enedi­amine)­nickel‐bis(μ‐hexa­cyano­iron‐N,N′)] trihydrate] and catena‐poly­[[tris­(ethyl­enedi­amine)­nickel‐bis(μ‐hexa­cyano­cobalt‐N,N′)] trihydrate], [{Ni(C₂H₈N₂)₂}₃{M(CN)₆}₂]·3H₂O, in which both cis and trans [Ni(en)₂] and [M(CN)₆] moieties are linked to give S‐shaped Ni–NC–M–CN–Ni–NC–M–CN–Ni units which are cross­linked to give ribbons parallel to the b axis. The two compounds are isomorphous with mean metal–ligand distances Fe—C = 1.940 (3), Co—C = 1.844 (3) and Ni—N = 2.102 (2) Å for the iron, and 2.105 (3) Å for the cobalt compound. These compounds appear to be identical with those formulated as [Ni(en)₂]₃[M(CN)₆]₂·2H₂O [Ohba, Maruona, Okawa, Enoki & Latour (1994). J. Am. Chem. Soc. 116 , 11566–11567; Ohba, Fukita & Okawa (1997). J. Chem. Soc. Dalton Trans. pp. 1733–1737] which were indexed on a smaller unit cell and described as disordered.