ELECTRON-SPIN-RESONANCE STUDIES OF THE METHANE RADICAL CATIONS ((CH4-C-12,13, (CDH3+)-C-12,13, (CD2H2+)-C-12, (CD3H+)-C-12, (CD4+)-C-12) INSOLID NEON MATRICES BETWEEN 2.5 AND 11 K - ANALYSIS OF TUNNELING())
Lb. Knight et al., ELECTRON-SPIN-RESONANCE STUDIES OF THE METHANE RADICAL CATIONS ((CH4-C-12,13, (CDH3+)-C-12,13, (CD2H2+)-C-12, (CD3H+)-C-12, (CD4+)-C-12) INSOLID NEON MATRICES BETWEEN 2.5 AND 11 K - ANALYSIS OF TUNNELING()), The Journal of chemical physics, 103(9), 1995, pp. 3377-3385
The radical cation of-methane isolated in neon matrices exhibits highl
y unusual electron spin resonance (ESR) spectral features between 2.5
and 11 K. The anomaly has been clarified by invoking large amplitude t
unneling motions of the hydrogens among several symmetrically equivale
nt Jahn-Teller distorted structures. The effect of the tunneling motio
ns upon the ESR spectrum was investigated by an analysis scheme based
upon permutation-inversion group theory. All the deuterium substituted
cations, i.e., CDH3+, CD2H2+, CD3H+, and CD4+ were also studied. The
hyperfine coupling constant of C-13 was obtained from the study of (CD
H3+)-C-13 and (CH4+)-C-13. Several independent generation methods were
employed during the course of these methane cation studies, including
photoionization, electron bombardment, x-irradiation, and a pulsed la
ser surface ionization technique. (C) 1995 American Institute of Physi
cs.