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Unpaired Electrons and Radical Stability

In the majority of heteroaromatic radicals the unpaired electron is in a fully delocalized molecular 7t-orbital. The magnetic moment of the unpaired electron is quantized in an applied magnetic field, which fact gives rise to [Pg.208]

the hyperfine splitting conferred on the ESR spectrum of a 7t-radical by interaction of the electron spin with a proton is proportional to the 7t-spin population p, at the atom bearing the proton (the McConnell relationship).17 Thus, for a proton attached to carbon atom i the hyperfine splitting a(H),-is given by Eq. (1), where QCH is the spin polarization parameter for the C—H bond. [Pg.209]

In many examples it is found that the contribution to a(N) from adjacent carbon atoms is small values of Q vary somewhat with the molecular orbital [Pg.209]

Carrington and A. D. McLachlan, Introduction to Magnetic Resonance. Harper, New York, 1967. [Pg.209]

Ayscough, Electron Spin Resonance in Chemistry. Methuen, London, 1967. [Pg.209]


See other pages where Unpaired Electrons and Radical Stability is mentioned: [Pg.205]    [Pg.208]   


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Electron radicals

Electron stability

Electronic stabilization

Electrons radicals and

Radicals stability

Stability, electronic

Stabilized electrons

Unpaired electron

Unpairing

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