Trinitromethyl-Substituted 1-1,2,4-Triazole Bridging Nitropyrazole: A Strategy of Utterly Manipulable Nitration Achieving High-Energy Density Material.

Nitro groups have been demonstrated to play a decisive role in the development of the most powerful known energetic materials. Two trinitromethyl-substituted 1-1,2,4-triazole bridging nitropyrazoles were first synthesized by straightforward routes and were characterized by chemical (MS, NMR, IR spectroscopy, and single-crystal X-ray diffraction) and experimental analysis (sensitivity toward friction, impact, and differential scanning calorimetry-thermogravimetric analysis test). Their detonation properties (detonation pressure, detonation velocity, etc.

Synthesis and detonation characters of 3,4,5-1-trinitropyrazole and its nitrogen-rich energetic salts.

The development of energetic materials is still facing challenges due to the inherent contradiction between energy and sensitivity. Two new nitrogen-rich energetic salts of 3,4,5-1-trinitropyrazole (HTNP) were synthesized. They are fully characterized by X-ray diffraction, NMR, MS and IR spectroscopy.

N-Site Regulation of Pyridyltriazole in Cp*Ir(N̂N)(HO) Complexes Achieving Catalytic FA Dehydrogenation.

A series of novel Cp*Ir complexes with nitrogen-rich N̂N bidentate ligands were developed for the catalytic dehydrogenation of formic acid in water under base-free conditions. These complexes were synthesized by using pyridyl 1,2,4-triazole, methylated species, or pyridyl 1,2,3-triazole as a N-site regulation ligand and were fully characterized. Complex bearing 1,2,4-triazole achieved a high turnover frequency of 14192 h at 90 °C in 4 M FA aqueous solution.

Precisely Controlling Ancillary Ligands to Improve Catalysis of Cp*Ir Complexes for CO Hydrogenation.

The regulation of ancillary ligands is critical to improve catalysis of Cp*Ir complexes for CO hydrogenation. Herein, a series of Cp*Ir complexes with N^N or N^O ancillary ligands were designed and synthesized. These N^N and N^O donors were derived from the pyridylpyrrole ligand.

Three-Dimensional Metal-Organic Frameworks as Super Heat-Resistant Explosives: Potassium 4,4'-Oxybis[3,3'-(5-tetrazol)]furazan and Potassium (1,2,4-Triazol-3-yl)tetrazole.

Heat-resistant explosives play an irreplaceable role in specialized applications. Two energetic metal-organic frameworks (EMOFs), potassium 4,4'-oxybis[3,3'-(5-tetrazol)]furazan and potassium (1,2,4-triazol-3-yl)tetrazole, featuring a three-dimensional metal-organic framework structure, were first synthesized and characterized by chemical (H NMR, C NMR, MS, IR spectroscopy, and single-crystal XRD) and physicochemical analyses (sensitivity toward friction, impact, electrostatic, and DSC-TGA test). The new 3D EMOFs were found to show high thermostability, highly positive heat of formation, and suitable sensitivities.

Ambient Cross-linking System Based on the Knoevenagel Condensation Reaction between Acetoacetylated Sucrose and Aromatic Dicarboxaldehydes.

An ambient cross-linking system based on the Knoevenagel condensation reaction between acetoacetylated sucrose and aromatic dicarboxaldehydes was demonstrated. In this study, we use a rheological instrument to measure the gel time to predict and elucidate the likely reaction mechanism of the system, and we prepare films based on the mechanistic results. Acetoacetylated sucrose and 4,4'-biphenyldicarboxaldehyde were used as raw materials, piperidine was used as the catalyst, and nonvolatile dimethyl sulfoxide (DMSO) was used as the solvent.

Extraordinarily large kinetic isotope effect on alkene hydrogenation over Rh-based intermetallic compounds.

A series of Rh-based intermetallic compounds supported on silica was prepared and tested in alkene hydrogenation at room temperature. H and D were used as the hydrogen sources and the kinetic isotope effect (KIE) in hydrogenation was studied. In styrene hydrogenation, the KIE values differed strongly depending on the intermetallic phase, and some intermetallic compounds with Sb and Pb exhibited remarkably high KIE values (>28).