M. Gramza et al., ELECTRON-SPIN RELAXATION AND ESEEM SPECTROSCOPY OF THE GLYCINE RADICAL IN DIGLYCINE NITRATE SINGLE-CRYSTAL, Acta chemica Scandinavica, 51(5), 1997, pp. 556-561
Glycine radical NH3+-CH-COO- produced by X-ray irradiation was identif
ied and characterized by cw-EPR and pulsed EPR methods. The isotropic
hyperfine coupling are: H-alpha=2.18 mT, H(NH3)=1.71 mT and N-14=0.3 m
T at 295 K. The spin lattice relaxation time was measured in the range
10-200 K by the saturation recovery method, and is described as the s
um of the contributions from the: direct process, distribution of the
inter-radical couplings and the Murphy process with vibrational energy
of 321 cm(-1). The phase memory time T-M was strongly temperature-dep
endent with two minima at 20 and 170 K related to the flipping motion
of the glycine molecules and rotation of the WH, groups, respectively.
The Fourier transform ESEEM spectrum consists of the proton matrix li
nes and very sharp lines in the nitrogen frequency region. They are in
terpreted as quadrupole frequencies under 'cancellation conditions' wi
th quadrupole coupling constant 2.10 MHz. an asymmetry parameter of 0.
7, and N-14 isotropic coupling a(iso)=2.12 MHz of the NH3-group of the
neighbouring glycine molecule.