Abstract
Trivalent phosphorus compounds, triphenylphosphine and triethyl phosphite, gave rise to dediazoniation of an arenediazonium salt in alcoholic solvent at ambient temperature in the dark. The reaction was well interpreted in terms of radical-chain mechanism initiated by an electron transfer from the trivalent phosphorus to a diazonium salt, which postulates a cation radical from the trivalent phosphorus as an intermediate.
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.
