Experimental and theoretical study of three new benzothiazole-fused carbazole derivatives.

Three new D-π-A type compounds, each containing one benzothiazole ring as an electron acceptor and one N-ethylcarbazole group as electron donor, were synthesized and characterized by elemental analysis, NMR, MS and thermogravimetric analysis. The absorption and emission spectra of three compounds were experimentally determined in several solvents and were simultaneously computed using density functional theory (DFT) and time-dependent density functional theory (TDDFT). The calculated reorganization energy for hole and electron indicates that three compounds are in favor of hole transport than electron transport.

[Research progress of ethanologenic Zymomonas mobilis].

Zymomonas mobilis is one of the natural ethanologenic microbes. With the unique Entner-Doudoroff pathway and some other special pathways of glycolytic and energetic metabolism, Z. mobilis has remarkable characters of higher rate of ethanol production and higher tolerance to ethanol.

[Synthesis and antibacterial activity of 2-(3-pyridyl)-5-([(5-aryl-1,3,4-oxadiazol-2-yl) methylene]thio)-1,3,4-oxadiazoles].

Aim: Studies on synthesis and antibacterial activity of new heterocycles.

Methods: The cyclocondensation of [(3-pyridyl)-1,3,4-oxadiazol-2-yl] thio acetic acid with various aroyl hydrazines in the presence of POCl3 and xylene gave the corresponding titled compounds, and the in vitro antibacterial activity was primarily evaluated by the method of cupplate diffusion solution.

Results: Sixteen novel titled compounds were synthesized, their structures were confirmed by IR, 1HNMR, MS and elemental analysis.