Spectroscopic, Crystallographic, and Electrochemical Study of Different Manganese(II)-Substituted Keggin-Type Phosphomolybdates.

Adjusting the RedOx activity of polyoxometalate catalysts is a key challenge for the catalysis of selective oxidation reactions. For this purpose, the possibility of influencing the RedOx potential by the introduction of an additional RedOx-active element was investigated. Thereby, Keggin-type polyoxometalates (POMs) with up to three different elements in the metal framework were created. An advanced and reproducible synthetic procedure to incorporate MnII and additionally VV into Keggin-type heteropolyacids alongside comprehensive characterization of the new molecules is presented. The success of our syntheses was confirmed by vibrational spectroscopy (IR and Raman) and elemental analysis. Furthermore, the new compounds were analyzed by NMR spectroscopy to investigate the characteristics of the POMs in solution. The structures of successfully crystalized compounds were determined by single-crystal X-ray diffraction. Moreover, all synthesized compounds were characterized using UV/Vis spectroscopy and electrochemical analysis to get further insights into the electronic transfer processes and redox potentials.

Reversible Oxidative Se-Se Coupling of Phosphine Selenides by Ph3 Sb(OTf)2.

Salts of diphosphoniumdiselenide dications ([R3 PSeSePR3 ][OTf]2 ) have been isolated from reactions of trialkylphosphine selenides with triphenylantimony bistriflate. The redox process is speculated to proceed via a cationic coordination complex [Ph3 SbL2 ][OTf]2 (L=Me3 PSe, iPr3 PSe), which is also formed in the reaction of [R3 PSeSePR3 ][OTf]2 with Ph3 Sb. The observations indicate that the reductive elimination of [R3 PSeSePR3 ]2+ from [Ph3 Sb(SePR3 )2 ]2+ is reversible through the oxidative addition of [R3 PSeSePR3 ]2+ to Ph3 Sb.

Heteroelements in polyoxometalates: a study on the influence of different group 15 elements on polyoxometalate formation.

In the field of polyoxometalate (POM) chemistry, different heteroelements are integrated into the cage-like structures, to obtain different structural types of so-called heteropolyanions (HPAs). While it is generally accepted, that some elements favor certain types of structure, a systematic study is still missing. In this article, we present a systematic investigation of the influence of the group 15 elements nitrogen, phosphorous, arsenic, and antimony on the formation of different POM structure types. Our study is comprised of DFT calculations and corresponding experimental structural analysis. In this context, the DFT study establishes the thermodynamics of formation of different coordination geometries with various heteroelements on two POM structure types, the Keggin and the Anderson-Evans structures. Our POM synthesis experiments were performed at two different pH values (1 and 5) and resulted in a variety of heteropolytungstates, which were identified and characterized by elemental analysis as well as single crystal X-ray diffraction and vibrational spectroscopy. With these methods, we were able to establish a clear trend, showing that heavier elements lead to formation of different structure types than lighter elements. These results signify a large step towards a better understanding of POM formation specifically with respect to the choice of heteroelement.

Supported H8PV5Mo7O40 on activated carbon: Synthesis and Investigation of influencing factors for catalytic performance.

Polyoxometalates (POMs), in particular the Keggin-type HPA-5 (H8PV5Mo7O40) are widely established as effective catalysts for acid- and redox-catalyzed reactions. Yet, they are mainly used as homogeneous catalysts, which poses challenges regarding catalyst separation. This study explores the synthesis of supported HPA-5, and its application as a heterogeneous catalyst for biomass conversion, focusing on activated carbons with diverse chemical and physical properties as support materials. Characterization of these carbons gives insights into the influence of surface area, oxygen content, and acidity on HPA adsorption and stability. Activated carbon CW20, was found to be the best support due to its high vanadium loading and effective preservation of the HPA-5 structure. It underwent various pre- and post-treatments, and the obtained supported catalysts were evaluated for their catalytic performance in converting glucose under both oxidative (OxFA process) and inert (Retro-Aldol condensation) conditions. Notably, HPA-5 supported on CW20 emerged as an exceptional catalyst for the retro-aldol condensation of glucose to lactic acid, achieving a selectivity of 15% and a conversion rate of 71%, with only minimal vanadium leaching.

Investigation of the Formation, Characterization, and Oxidative Catalytic Valorization of Humins.

The industrial use of biomass, e.g., for the production of platform chemicals such as levulinic acid, became increasingly important in recent years. However, the efficiency of these processes was reduced by the formation of insoluble solid waste products called humins. Herein, the formation of humins from various carbohydrates was investigated under different process conditions, in order to obtain information about the structure and the formation mechanism. During this process, new potential structural fragments of humins were identified. Subsequently, the produced humins were oxidatively converted to low-molecular-weight carboxylic acids with the use of polyoxometalate catalysts. The experiments showed that the use of sugars in acetic acid and ethanol only lead to the formation of a small amount of humins, which were also structurally most suitable for conversion to carboxylic acids. The main products of the oxidative valorisation of these humins were acetic acid, formic acid, and CO2, respectively, and our results indicate that certain functional groups were converted preferentially. These findings will help to improve processes for the valorisation of biomass by enabling an overall more efficient use of thermo-sensitive feedstock such as carbohydrates.

H8 [PV5 Mo7 O40 ] - A Unique Polyoxometalate for Acid and RedOx Catalysis: Synthesis, Characterization, and Modern Applications in Green Chemical Processes.

Polyoxometalates (POMs) are a fascinating group of anionic metal-oxide clusters with a broad variety of structural properties and several catalytic applications, especially in the conversion of bio-derived platform chemicals. H8 [PV5 Mo7 O40 ] (HPA-5) is a unique POM catalyst that ideally links numerous fascinating research fields for the following reasons: a) HPA-5 can be synthesized by rational design approaches; b) HPA-5 can be well characterized using multiple analytical tools explaining its catalytic properties; and c) HPA-5 is suitable for multiple important catalytic transformations of bio-based feedstock. This Review combines the fields of synthesis, spectroscopic, electrochemical, and crystallographic characterization of HPA-5 with those of sustainable catalysis and green chemistry. Selected catalytic applications include esterification, dehydration, and delignification of biomass as well as selective oxidation and fractionation of bio-based feedstock. The unique HPA-5 is a fascinating POM that has a broad application scope for biomass valorization.

Revealing the nitrogen reaction pathway for the catalytic oxidative denitrification of fuels.

Aside from the desulfurisation, the denitrogenation of fuels is of great importance to minimze the environmental impact of transport emissions. The oxidative reaction pathway of organic nitrogen in the catalytic oxidative denitrogenation could be successfully elucidated. This is the first time such a pathway could be traced in detail in non-microbial systems. It was found that the organic nitrogen is first oxidized to nitrate, which is subsequently reduced to molecular nitrogen via nitrous oxide. Hereby, the organic substrate serves as a reducing agent. The discovery of this pathway is an important milestone for the further development of fuel denitrogenation technologies.

A study of cyanotetrazole oxides and derivatives thereof.

In this work we report on the syntheses of energetic salts of cyanotetrazolate-1- and -2-oxides; this offers a unique ability to compare the effects of tetrazole 1- versus 2-oxidation. 5-Cyanotetrazolate-2-oxide can be synthesized by oxidation of the 5-cyanotetrazolate anion with Oxone, while the corresponding 1-oxide was synthesized by the rearrangement of azidoaminofurazan. Both chemical (multinuclear NMR, IR, and Raman spectroscopies, mass spectrometry, etc.) as well as explosive (impact, friction, and static sensitivities) properties are reported for these energetic salts. Calculated explosive performances using the EXPLO5 computer code are also reported. We furthermore detail the chemistry of these two anions, and their ability to form tetrazole-carboxamides, dihydrotetrazines, and tetrazines. The ability to hydrolyze cyanotetrazole oxides to their amides was demonstrated by two copper complexes. Several crystal structures of these species are presented in addition to full chemical characterization. Finally, the unique 1,4,-bis(2-N-oxidotetrazolate)-1,2,4,5-tetrazine anion was characterized as an energetic material as its ammonium salt.