It has been found that x-irradiation of a single crystal of glutaconic acid (HOOC)CH=CH–CH2(COOH) produces the oriented allyl-type free radical (HOOC)C(1)H=C(2)H–C(3)H(COOH). A detailed analysis of the electron magnetic resonance spectra of this radical confirms that the spin density on carbon 2 is opposite in sign to the spin densities on carbons 1 and 3. Additional structural features determined are: (a) The unpaired electron occupies a delocalized π molecular orbital extending over carbon atoms 1, 2, and 3; (b) spin densities ρii for carbon p orbitals on carbon atoms 1, 2, and 3 are ρ11=ρ33=+0.57, ρ22=−0.19; (c) principal values of the hyperfine tensors for protons 1 and 3 are −53, −36, and −18 Mc, and for proton 2 are +17, +12, +7 Mc; (d) all C–H bonds in the radical are nearly parallel. The parallelism of all C–H bonds indicates that the undamaged parent molecule is the trans isomer of the acid.
No takes yet. Share an insight, caveat, or question.
Heller et al. (1962) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: