Abstract
In the action of diazonium salts on 5-alkylidenerhodanines, azo compounds are formed by the replacement of one or two hydrogen atoms in the methyl group. In the case of 5-ethylidenerhodanines, the formation of an azorhodanine through the replacement of the alkylidene residue by an arylazo group takes place simultaneously. In the formazyl derivatives the long-wave absorption maximum is displaced hypsochromically by 15–20 nm as compared with the dyes having a single azo group.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
