Zirconia-supported 11-molybdovanadophosphoric acid catalysts: effect of the preparation method on their catalytic activity and selectivity.

The oxidation of adamantane with hydrogen peroxide catalyzed by zirconia-supported 11-molybdovanadophosphoric acid is shown to be a suitable green route for the synthesis of adamantanol and adamantanone. This work evaluates how the catalyst activity and selectivity are affected by some of its preparative parameters, such as the method for supporting the catalytically active heteropoly acid over the zirconia matrix or the pretreatments applied to the resulting materials before being used as heterogeneous catalysts. Our results indicate that the most effective catalysts able to maintain their activity after several reaction runs are those prepared by following the sol-gel route, whereas the most selective catalysts are those obtained by impregnation methods.

A Simple Approach To Develop Tailored Mesoporosity in Nanostructured Heteropolysalts.

In this study, we describe a very simple approach to the development of tailored mesoporosity in any nanostructured heteropolysalt with control over both the mesoporous volume and the pore size. This approach, which consists in the treatment of a solid microporous precursor with a basic agent, has been tested on the ammonium salt of the Keggin-type [PMo O ] heteropolyanion and constitutes a novel procedure for the preparation of mesoporous solids with no precedents. The results obtained in this study allow two main conclusions to be drawn: 1) the micro- and mesoporous structures in the heteropolysalt nanoparticles are independent from each other and 2) the development of mesoporosity in the solid material must be related to a process of alkaline degradation within the core of the nanocrystals that aggregate into the particles.

A Robust Open Framework Formed by Decavanadate Clusters and Copper(II) Complexes of Macrocyclic Polyamines: Permanent Microporosity and Catalytic Oxidation of Cycloalkanes.

The first decavanadate-based microporous hybrid, namely, [Cu(cyclam)][{Cu(cyclam)}2(V10O28)]·10H2O (1, cyclam = 1,4,8,11-tetraazacyclotetradecane) was prepared by reaction of (VO3)(-) anions and {Cu(cyclam)}(2+) complexes in NaCl (aq) at pH 4.6-4.7 and characterized by elemental analyses, thermogravimetry, and X-ray diffraction (powder, single-crystal) techniques.

Transcriptional organization of genes for protocatechuate and quinate degradation from Acinetobacter sp. strain ADP1.

Quinate and protocatechuate are both abundant plant products and can serve, along with a large number of other aromatic or hydroaromatic compounds, as growth substrates for Acinetobacter sp. strain ADP1. The respective genes are part of the chromosomal dca-pca-qui-pob-hca cluster encoding these pathways.

Differential DNA binding of transcriptional regulator PcaU from Acinetobacter sp. strain ADP1.

Transcriptional regulator PcaU from Acinetobacter sp. strain ADP1 governs expression of genes for protocatechuate degradation (pca genes) as a repressor or an activator depending on the levels of the inducer protocatechuate and of its own gene. PcaU is a member of the IclR protein family.