𝔖 Bobbio Scriptorium
✦   LIBER   ✦

EPR parameters of radical ions and polarizability effect

✍ Scribed by Alexey N. Egorochkin; Olga V. Kuznetsova; Nadiya M. Khamaletdinova; Lada G. Domratcheva-Lvova


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
178 KB
Volume
49
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The literature data on substituent influence on the g factors, hyperfine coupling (hfc) constants (a) of the EPR signals and the spin densities (ρ) have been analyzed for 25 series of the organic radical cations and radical anions as well as of the transition metal complexes. The g, a, and ρ values were first established to depend not only on the inductive and resonance effects but also on the polarizability of substituents which can be characterized by the Οƒ~Ξ±~ constants. The polarizability effect is caused by the partial charge on the radical center. This effect consists in an electrostatic attraction between the charge and the dipole moments induced by this charge in the substituents. The polarizability contribution ranges up to 92%. Copyright Β© 2011 John Wiley & Sons, Ltd.


πŸ“œ SIMILAR VOLUMES


EPR Study of the Radical Ions of Aryl-Su
✍ Crockett, Rowena ;Gescheidt, Georg ;Dyker, Gerald ;KΓΆrning, Jutta πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English

## Abstract The radical anions and the radical cations of 1–3 in which three Ο€ systems are connected in three dimensions by a strained propellane spacer were studied by ESR/ENDOR/TRIPLE spectroscopy. The hyperfine data of acenaphthene (4) are compared with those of the fused Ο€ systems 5–10. In the

Cycloheptatrienyl radicals: An EPR study
✍ Finlay MacCorquodale; John C. Walton πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 513 KB

## Abstract Cycloheptatrienyl radicals with donor and acceptor substituents were generated by hydrogen abstraction from the corresponding cycloheptatrienes and studied by EPR spectroscopy. The barrier to rotation about the C‐1ο£ΏCο£ΎO bond in ethoxycarbonylcycloheptatrienyl radicals was found to be ca.