Pt/TiO2 was prepared by impregnation method and characterized with XRD、 BET and XRD results showed TiO2 as prepared was anatase and the average particle sizewas about17 nm.The results of the photocatalytic degradatio...Pt/TiO2 was prepared by impregnation method and characterized with XRD、 BET and XRD results showed TiO2 as prepared was anatase and the average particle sizewas about17 nm.The results of the photocatalytic degradation of 3-methyl indole suggested that the influences of Pt amount and loading amount of catalytics have obvious effect to catalyst activity.The concentration of flow rate and consistence obviously influenced the 3-methyl indole photocatalytic degradation.展开更多
The coupling reaction of 3-cyanoacetyl-2-methylindole 1a with the aromatic diazonium salts gave the corresponding arylhydrazones 2a-e. Compounds 2 were used for synthesis of 4-aminopyrazole-5-carbonitrile 4a-e and 5-a...The coupling reaction of 3-cyanoacetyl-2-methylindole 1a with the aromatic diazonium salts gave the corresponding arylhydrazones 2a-e. Compounds 2 were used for synthesis of 4-aminopyrazole-5-carbonitrile 4a-e and 5-amino-4-arylazo-3-pyrazoles 5a-e derivatives. Also, treatment of 3-cyanoacetyl-2-phenylindole 1b with phenyl isothiocyanate gave the corresponding thioacetanilide 7. The later compound 7 was utilized as the key intermediate for the synthesis of some new thiadiazole derivatives 9a-r. The structures of all new compounds were elucidated on the basis of elemental analysis and spectral data.展开更多
文摘Pt/TiO2 was prepared by impregnation method and characterized with XRD、 BET and XRD results showed TiO2 as prepared was anatase and the average particle sizewas about17 nm.The results of the photocatalytic degradation of 3-methyl indole suggested that the influences of Pt amount and loading amount of catalytics have obvious effect to catalyst activity.The concentration of flow rate and consistence obviously influenced the 3-methyl indole photocatalytic degradation.
文摘The coupling reaction of 3-cyanoacetyl-2-methylindole 1a with the aromatic diazonium salts gave the corresponding arylhydrazones 2a-e. Compounds 2 were used for synthesis of 4-aminopyrazole-5-carbonitrile 4a-e and 5-amino-4-arylazo-3-pyrazoles 5a-e derivatives. Also, treatment of 3-cyanoacetyl-2-phenylindole 1b with phenyl isothiocyanate gave the corresponding thioacetanilide 7. The later compound 7 was utilized as the key intermediate for the synthesis of some new thiadiazole derivatives 9a-r. The structures of all new compounds were elucidated on the basis of elemental analysis and spectral data.
