Papers by Keyword: Pyrazole

Abstract: A series of new nitropyrazole explosive molecules were designed with N-nitropyrazole as structural unit, The detonation parameters of nitropyrazoles explosives, such as detonation velocity, detonation pressure, detonation temperature, detonation volume, were estimated theoretically in different methods, The calculated detonation pressure was corresponded with high energy density material (HEDM). Their detonation velocity and detonation pressure are between those of TATB and HMX. These compounds have higher detonation temperature and heat of detonation compared with HMX and TATB. It was predicted that these explosives are of favorable stability.

Abstract: In order to explore high strength organic electrotransporting electroluminescent (EL) materials, twelve new pyrazole oxadiazole compounds containing the benzothiazole or benzene group in the 1 position of pyrazole, the aromatic group in the 3 position of pyrazole and the formacyl group in the 4 position of pyrazole were designed and synthesized. A new method of synthesizing 1,3,4-oxadiazole compound was described. Their structures were characterized by IR, MS, ¹H NMR spectra and elemental analysis. The fluorescence properties were measured by fluorometry. The results showed that the target compounds had good fluorescence and λ_em ranged from 410nm to 450 nm and fluorescence quantum yields up to 0.69.

Abstract: The reaction of 1,4,5,6-tetrahydro-6-pyridazinone-3-carboxylic acid hydrazides (1) and 1,6-dihydro-6-pyridazinone-3-carboxylic acid hydrazides (2) with four kind of substituted 3-formyl chromones (3a-3d) and five kind of 1-phenyl-3-aryl-4-formylpyrazoles (3e-3i) afforded the new compounds aldehyde hydrazones (4a-4i) and (5a-5i). Their structures were established by IR, ¹H NMR and elemental analysis.

Abstract: A novel photochromic diarylethene based on pyrazole moiety was synthesized and its photochromic and fluorescent properties were also investigated. The compound exhibited remarkable photochromism, changing from colorless to purple after irradiation with UV light both in solution and in PMMA film. In hexane solution and in PMMA film, the open-ring isomer of the diarylethene 1 exhibited relatively remarkable fluorescence. The results indicated that the pyrazole moiety played a very important role during the process of photochromic reaction for the diarylethene derivative. Using this dithienylethene 1c as optical storage was performed successfully.