Volume 17 (1969) Issue 4 Pages 661-668
Several compounds possessing both mercapto and hydroxyimino groups, such as 2-mercaptoacetophenone oxime, 3-mercaptopropiophenone oxime and 5-nitro-2-mercapto-benzaldehyde oxime, were prepared, and their reactivities with metal ions were compared with those of the corresponding ketones or aldehyde and those of thiohydroxamic acids. It was found that these compounds did not show any sensitive color reactions with Fe3+, Ti4+, UO2+2 and VO2+ and did not form stable Fe3+ and Cu2+ complexes, differing from thiohydroxamic acids, and that the conversions of the compounds possessing both carbonyl and mercapto group to the corresponding oximes did not give any effect on the sensitivities and selectivities.