Cation directed formation of uranyl phosphonocarboxylates frameworks comprised of cross-linked chains

Three new uranyl phosphonate frameworks with barium or lead were hydrothermally synthesized using phos-phonoacetate and phosphonopropionate ligands. The first two frameworks are made up of cross-linked chains that are comprised of uranyl pentagonal bipyramids connected by the three oxygen atoms of the phosphonate tetra-hedra. The carboxylates of the ligands bond to the uranyl ions of other chains to form the perpendicular rows that comprise the framework. The third framework is similar to the first, being comprised of interpenetrating chains. However, the longer carbon chain of the phosphonopropionate allows for a less strained packing of the chains. The crystallization of the barium uranyl phosphonate framework was investigated as a function of iron concen-tration using scanning electron microscopy. The use of iron to grow larger crystals of the phosphonoacetate lead framework is also described. The barium containing framework was found to disassociate in water with the chains disassociating from each other.

Automated summary

Three new uranyl phosphonate frameworks with barium or lead were synthesized hydrothermally using specific ligands. The structures of these frameworks were analyzed and compared, revealing different cross-linked chains and packing arrangements. The effect of iron concentration on the crystallization of a barium uranyl phosphonate framework was investigated, as well as the use of iron to grow larger crystals of a phosphonoacetate lead framework. The dissociation of the barium-containing framework in water was also observed.