Diverse reactivity of a cationic N-heterocyclic phosphenium complex towards anionic substrates – substitution vs. reduction
Year: 2024
Type: article
Abstract: , which proceed not only by complexation of the P-donors as expected, but involve also oxidative addition steps and single electron transfer processes in which excess iron complex acts as the reductant. The title complex and the products isolated in the reaction studies were characterised by spectroscopic data and in many cases by XRD studies. Computational studies were employed to analyse the differing reactivity of the cationic NHP complex towards light and heavy halide ions, and to help in the assignment of the radical intermediate observed. The more diverse reactivity of the cationic NHP complexes compared to their neutral analogues is attributed to their higher electrophilicity.
Source: Dalton Transactions
DOI: 10.1039/d4dt03352c
Institutions: University of Stuttgart, University of Helsinki
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
OpenAlex ID: W4405829198
