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Ben E Cockbain

Publications and source records attributed to Ben E Cockbain.

2 recordsLinked to original sources

Structural variation in organically templated uranium sulfate fluorides.

The ability of templated uranium sulfate fluorides to adopt diverse inorganic architectures is demonstrated in six novel materials. The inorganic structures present in [N2C6H16][UO2F2(SO4)](USFO-2), [N2C6H16][UO2F(SO4)]2(USFO-3), [N2C3H12][UO2F(SO4)]2.H2O (USFO-4), [N2C5H14][UO2F(H2O)(SO4]2(USFO-5), [N2C6H18]2[UO2F(SO4)]4.H2O (USFO-6) and [N2C3H12][UO2F(SO4)]2.H2O (USFO-7) range from infinite chains to five different layer topologies. The chain, and two of the five layers, have unprecedented structure types. These compounds illustrate the structural diversity within this new family of materials, arising from the varied coordination of the U6+ centres. Each material was synthesised under hydrothermal conditions, through reaction of uranyl acetate, sulfuric acid, HF(aq), water, and the respective organic template.

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The effects of hydrofluoric acid addition on the hydrothermal synthesis of templated uranium sulfates.

The effect of employing hydrofluoric acid as a mineraliser in the formation of organically templated uranium sulfate materials has been studied. Variable amounts of HF((aq)) were added to a series of reaction gels in which all other reactant concentrations were invariant, resulting in the formation of three different phases, depending upon the fluoride concentration. Two of these phases are novel; [N(2)C(4)H(14)][UO(2)(H(2)O)(SO(4))(2)] is a new templated uranium sulfate, containing anionic [UO(2)(H(2)O)(SO(4))(2)](2-) chains that hydrogen bond to one-another forming pseudo-layers, and [N(2)C(4)H(14)][UO(2)F(SO(4))](2) is the first example of a templated uranium sulfate fluoride, which consists of uranium fluoride chains linked by sulfate groups to form [UO(2)F(SO(4))](-) layers. The role of F(-) in these reactions is two-fold; it acts as a mineraliser when present in small concentrations, while it is incorporated into the reaction product when present in larger mole fractions. Both of the new materials have been characterised using a range of physical techniques including single crystal X-ray structure analysis.

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