Research on the Influence of Cosolvent on the Determination of the Contamination Degree of Jet Fuel.

The effect of cosolvent on trace free water in the determination of the contamination degree of jet fuel was investigated. The interference of trace free water on the automatic particle counter can be eliminated by adding isopropanol as a cosolvent to the measured oil sample. Isopropanol can dissolve trace free water in oil. Addition of isopropanol could stabilize the pollution grade of particles with size ≥30 µm (c) at the same level, which is most obviously affected by free water without isopropanol. The standard uncertainty u(X 1) is slightly reduced with the addition of isopropanol, and the repeatability and accuracy of the automatic particle counting method are obviously improved. The results show that isopropanol should be added as a cosolvent to eliminate the interference of free water when the contamination degree of jet fuel oil samples with obvious free water is determined by the automatic particle counting method.

I2-Mediated Iodobenzannulation of Yne-Allenones toward 1-Naphthols and Their Synthetic Application.

A new I2-mediated iodobenzannulation of yne-allenones has been established, enabling breaking/rearranging of C≡C bonds to selectively access 4-iodonaphthalen-1-ols with generally good yields. The resulting 4-iodonaphthalen-1-ols could serve as a new and reliable coupling reagent, which further reacted with H2O under the oxygen conditions to generate unexpected 1,2-carbonyls with good yields through Pd-catalyzed deiodinated carbonylation, whereas employment of benzene-1,2-diamine as the nucleophile rendered 3-(quinoxalin-2-yl)naphthalen-1-ols through Pd-catalyzed [4 + 2] heterocyclization. On the basis of the controlled experiments, the mechanism for forming 1,2-carbonyls was proposed, including an oxidative addition, 1,3-palladium migration, reductive elimination, and oxidative dehydrogenation sequence.

Atom-economic synthesis of cyclobuta[a]naphthalen-4-ols via a base-promoted [2 + 2] cycloaddition/1,6-nucleophilic addition cascade.

A first atom-economic [2 + 2] cycloaddition/1,6-conjugate addition cascade of yne-allenones with C-nucleophiles including 1,3-dicarbonyls and α,α-dicyanoolefins under base-promoted conditions has been established, enabling the direct construction of C(sp3)-C(sp3) bonds to generate cyclobuta[a]naphthalen-1-ols with generally good yields. These resulting products have a cyclobutene unit that contains both an aryl and alkyl group.