A series of novel monoazo-disperse dyes containing pyrazolo[1,5-a]pyrimidine structures were synthesized starting with the coupling reaction between ethyl cyanoacetate and 4-hydroxybenzenediazonium chloride, followed by treatment of the resulting hydrazone product with hydrazine hydrate. The pyrazolohydrazone 6 is then treated with either 2,4-pentandione and enaminonitrile or aryl-substituted enaminoketones to give the target pyrazolo[1,5-a]pyrimidine dyes 7 and 15a-d. Structural assignments to the dyes were made using NMR spectroscopic methods. A new high temperature method, using microwave heating, was employed to apply these dyes to polyester fibers. Most of the dyed fabrics tested displayed moderate light fastness and excellent washing fastness properties.

A series of new monoazo disperse dyes containing pyrazolopyrimidine moieties was synthesized by coupling malononitrile or 3-aminocrotononitrile with 4-hydroxy- benzenediazonium chloride. Treatment of the resulting products with hydrazine hydrate yields the corresponding 4-arylazoaminopyrazoles, which then react with either 2,4-pentanedione and enaminonitriles or aryl-substituted enaminoketones to give the target pyrazolopyrimidine monoazo disperse dyes. Structural assignments of the dyes were made using both NMR spectroscopic and X-ray crystallographic methods. A high temperature dyeing method, by microwave irradiation, was employed with polyester fabrics. Most of the dyed fabrics tested displayed moderate light fastness and excellent washing and perspiration fastness levels.

No abstract

No abstract

No abstract

No abstract

Irradiation of benzotriazoles 1a-e at λ = 254 nm in acetonitrile solution generated the corresponding 1,3-diradicals which underwent intermolecular cycloaddition with maleimides to afford the corresponding dihydropyrrolo [3,4-b]indoles and with acetylene derivatives to afford indoles as the major products. This offers an interesting and simple access to such ring systems of potential synthetic and biological interest. The structures of the photoproducts were established spectroscopically and by single crystal X-ray crystallography.

A new method was proposed for the application of azole corrosion inhibitors on the surface of copper. This method depends on the vacuum pyrolysis of the inhibitor in the presence of copper specimens. Three azole inhibitors namely; benzotriazole (Azole (1) (2)) and N-[Benzotriazol-1-yl-(4-methoxy-phenyl)-methylene]-N-phenyl-hydrazine (Azole (3)) were tested. After pyrolysis copper samples were electrochemically tested in sulfide polluted salt water and compared to the behavior of copper tested in the sulfide polluted salt water containing dissolved benzotriazole. Results showed that copper specimens treated in the presence of Azoles (2) and (3) exhibit excellent corrosion resistance. Those samples could resist the poisoning effect of sulfide ions. Azole (1) shows good resistance at low sulfide concentration and failed at the high concentration. Surface investigation support the results of electrochemical tests.