Homogeneous and Heterogeneous Anion Sensing by a Molecular Cobalt-Vanadium Oxide.

Spectroscopic anion sensing is a vital non-invasive tool in chemistry and biology. Here, a molecular cobalt-vanadium-oxide cluster was shown to be capable of selectively binding and detecting various mono-anions in solution and immobilized on a solid support. The cluster anion [Co(X)V O ] (X=mono-anion, for example, halide, pseudohalide, carboxylate, etc.

A new class of homogeneous visible-light photocatalysts: molecular cerium vanadium oxide clusters.

The first systematic access to molecular cerium vanadium oxides is presented. A family of structurally related, di-cerium-functionalized vanadium oxide clusters and their use as visible-light-driven photooxidation catalysts is reported. Comparative analyses show that photocatalytic activity is controlled by the cluster architecture.

The anion-binding polyanion: a molecular cobalt vanadium oxide with anion-sensitive visual response.

An anionic molecular cobalt vanadium oxide cluster, (n-Bu4N)3[Co(AcO)V4O12] and its use as anion binding site is reported. Cluster formation is controlled by an anion-dependent dynamic solution equilibrium. Reversible anion binding in solution leads to significant spectral changes, allowing the ratiometric optical detection of the anion concentration in situ, even under harsh thermal conditions (T = 90 °C).

Chirality meets visible-light photocatalysis in a molecular cerium vanadium oxide cluster.

The first example of a molecular cerium vanadium oxide photocatalyst is presented. A cerium vanadium oxide cluster, (nBu4N)2[(Ce(dmso)3)2V(IV)V(V)11O33Cl] × 2DMSO (1), was obtained by bottom-up self-assembly. The compound exhibits high visible-light photooxidative activity towards indigo with quantum efficiencies >10%.

Polytypism and oxo-tungstate polyhedra polymerization in novel complex uranyl tungstates.

Three new uranyl tungstates, α-, β-Cs(2)[(UO(2))(2)(W(2)O(9))], and Rb(6)[(UO(2))(7)(WO(5))(2)(W(3)O(13))O(2)], have been obtained by high temperature solid state reactions. All three compounds display novel structure topologies: α- and β-Cs(2)[(UO(2))(2)(W(2)O(9))] are based upon layers with a new topology that can be related to the uranophane topology; Rb(6)[(UO(2))(7)(WO(5))(2)(W(3)O(13))O(2)] is a rare example of a non-molecular inorganic phase with layers containing oxo-tungstate trimers. The structural relationship between α- and β-Cs(2)[(UO(2))(2)(W(2)O(9))] can be assigned to polytypism.