An ESR investigation of the thermal hydrophosphination of 1-hexyne by five different secondary phosphines and phosphine-boranes did not lead to the observation of any radical, but in the presence of the spin trap MNP (2-methyl-2-nitrosopropane) several phosphonitroxides were detected. The unusually low phosphorus splitting exhibited by some of these species could be accounted for on the basis of DFT calculations. Although two phospho-substituted vinyl nitroxides were identified in the course of the hydrophosphination reaction, they could not be considered as evidence of the direct involvement of phosphorus-centred radicals. © The Royal Society of Chemistry.

An ESR and DFT revisitation of phosphonitroxides prompted by an ineffective ESR approach to the hydrophosphination of alkynes

Alberti A;Guerra M;Venturini A
2013

Abstract

An ESR investigation of the thermal hydrophosphination of 1-hexyne by five different secondary phosphines and phosphine-boranes did not lead to the observation of any radical, but in the presence of the spin trap MNP (2-methyl-2-nitrosopropane) several phosphonitroxides were detected. The unusually low phosphorus splitting exhibited by some of these species could be accounted for on the basis of DFT calculations. Although two phospho-substituted vinyl nitroxides were identified in the course of the hydrophosphination reaction, they could not be considered as evidence of the direct involvement of phosphorus-centred radicals. © The Royal Society of Chemistry.
2013
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
ELECTRON-SPIN-RESONANCE; PRIMARY PHOSPHINE-BORANES; CROWDED TRIARYLPHOSPHINES; REDOX PROPERTIES; ANODIC BEHAVIOR; RADICALS; DERIVATIVES; DENSITY; ACCESS; TRAPS
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/314774
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 3
  • ???jsp.display-item.citation.isi??? ND
social impact