The sensitive and selective detection of nitroaromatic explosives is great significance to national security human health. Herein, the novel linear polymer l-PAnTPE cross-linked PAnTPE nanoparticles based on anthracene tetraphenylethene groups were designed successfully synthesized via Suzuki-miniemulsion polymerization. particle sizes polymers are around 73 nm, making them well dispersible in ...

We investigated the fluorescence properties of dye aggregates formed in a poly(vinylalcohol) (PVA) matrix by phase separation. Trimethyl-(2-oxo-2-pyrene-1-yl-ethyl)-ammonium bromide (PyAm) was used as a fluorescent dye molecule. The size of PyAm aggregates in the PVA thin films were increased with increasing dye concentration, which was confirmed by atomic force microscope (AFM) measurements. T...

Nitroreductases (NRs) hold promise for converting nitroaromatics to aromatic amines. Nitroaromatic reduction rate increases with Hammett substituent constant for NRs from two different subgroups, confirming substrate identity as a key determinant of reactivity. Amine yields were low, but compounds yielding amines tend to have a large π system and electron withdrawing substituents. Therefore, we...

N-substituted aromatics are important priority pollutants entering the environment primarily through anthropogenic activities associated with the industrial production of dyes, explosives, pesticides, and pharmaceuticals. Anaerobic treatment of wastewaters discharged by these industries could potentially be problematical as a result of the high toxicity of N-substituted aromatics. The objective...

The electroanalytical techniques of pulse polarography, stripping voltammetry and on-line electrochemical detection have been used for the identification and determination of trace concentrations of a wide variety of environmentally significant organic molecules, usually after the application of sample pretreatment procedures, certain separation techniques and, in some cases, derivatisation. Cl...

An efficient Pd catalyst for the transformation of aryl chlorides, triflates, and nonaflates to nitroaromatics has been developed. This reaction proceeds under weakly basic conditions and displays a broad scope and excellent functional group compatibility. Moreover, this method allows for the synthesis of aromatic nitro compounds that cannot be accessed efficiently via other nitration protocols...