Abstract
The reaction of m-chloroperbenzoic (m-CPBA) acid with meso-tetrakis (pentafluorophenyl) porphynatoiron(III) chloride (F20TPPFe(III)Cl ) has been studied in dichloromethane and acetonitrile medium at 25 ± 1°C. The reactive intermediates formed in this reaction have been quantitatively trapped by 2,4,6-tri t-butylphenol (TTBP) in both the solvents. It has been observed that the kinetic plots of the formation of TTBP• radical in dichloromethane are all multiexponential, supporting the formation of more than one reactive intermediate in this solvent. In acetonitrile solvent the formation of TTBP• radical was however observed to be distinctly single exponential. Different kinds of reactive intermediates are proposed in these two solvents.
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.
