A mechanism for the aziridination of olefins by aryl azides (ArN3), promoted by ruthenium(ii) porphyrin complexes, is proposed on the basis of kinetic and theoretical studies. All the recorded data support the involvement of a mono-imido ruthenium complex as the active intermediate in the transfer of the nitrene moiety "ArN" to the olefin. The selectivity of the aziridination vs. the uncatalysed triazoline formation can be enhanced by fine-tuning the electronic features of the porphyrin ligand and the olefin/azide catalytic ratio. The DFT study highlights the importance of an accessible triplet ground state of the intermediate ruthenium mono-imido complex to allow the evolution of the aziridination process.

A mechanistic investigation of the ruthenium porphyrin catalysed aziridination of olefins by aryl azides / Zardi, P.; Pozzoli, A.; Ferretti, F.; Manca, G.; Mealli, C.; Gallo, E.. - In: DALTON TRANSACTIONS. - ISSN 1477-9226. - 44:22(2015), pp. 10479-10489. [10.1039/c5dt00951k]

A mechanistic investigation of the ruthenium porphyrin catalysed aziridination of olefins by aryl azides

Zardi P.;
2015-01-01

Abstract

A mechanism for the aziridination of olefins by aryl azides (ArN3), promoted by ruthenium(ii) porphyrin complexes, is proposed on the basis of kinetic and theoretical studies. All the recorded data support the involvement of a mono-imido ruthenium complex as the active intermediate in the transfer of the nitrene moiety "ArN" to the olefin. The selectivity of the aziridination vs. the uncatalysed triazoline formation can be enhanced by fine-tuning the electronic features of the porphyrin ligand and the olefin/azide catalytic ratio. The DFT study highlights the importance of an accessible triplet ground state of the intermediate ruthenium mono-imido complex to allow the evolution of the aziridination process.
44
22
10479
10489
A mechanistic investigation of the ruthenium porphyrin catalysed aziridination of olefins by aryl azides / Zardi, P.; Pozzoli, A.; Ferretti, F.; Manca, G.; Mealli, C.; Gallo, E.. - In: DALTON TRANSACTIONS. - ISSN 1477-9226. - 44:22(2015), pp. 10479-10489. [10.1039/c5dt00951k]
Zardi, P.; Pozzoli, A.; Ferretti, F.; Manca, G.; Mealli, C.; Gallo, E.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1285857
Citazioni
  • ???jsp.display-item.citation.pmc??? 4
  • Scopus 29
  • ???jsp.display-item.citation.isi??? 28
social impact