Reply to "Comment on Electron Spin Resonance of oxygen-16-oxygen

Spin Resonance of oxygen-16-oxygen-17, oxygen-17-oxygen-18, and oxygen-18-oxygen-16 by Carrington, Levy, and Miller" ... Publication Date: June 19...
0 downloads 0 Views 128KB Size
COMMUNICATIONS TO THE EDITOR

2373

AJ = k 2 transitions, which are allowed in a magnetic field, to occur at considerably less than 5500 gauss a t X-band frequencies. These are the lines observed by Keys. The suggestion by Keys that some of the lines below 5500 gauss arise from the isotopic species 016-0”and 0 1 7 - 0 1 * deserves comment on other grounds. The natural abundance of 0 17-018 is approximately 0.016%. Taking into account the sixfold hyperfine splitting from 0 1 7 (i.e., 21 1, not 2S(S 1) as given by Keys), lines implies a signal-to-noise observation of 0 17-01* ratio of approximately lo6 to 1 for some of the 0l6-Ol6 lines. On the basis of our experience with a Varian 100-kc epr spectrometer, Keys’ hopes of 017-018 resonances, even a t 77”K, are about three orders of magnitude too optimistic.

+

+

DEPARTMENT OF THEORETIC.4L UNIVERSITY OF CAMBRIDGE ENGLAND CAMBRIDGE,

CHEMISTRY

A.

CARRINGTON

D. H. LEVY T. A. MILLER

ACCEPTED ANI) TRANSMITTED BY THEFARADAY SOCIETY

DECEMBER 22, 1966

there are still discrepancies in the various theories to explain the absorption peaks. In view of the recent observation of the hfs of 0 1 7 in SiOJ7and the high spin molecular density of oxygen, it is believed that 0 1 7 can contribute to the observed esr spectra of oxygen. The reported possible 01“017 transitions would be naturally very weak and are believed only to contribute possibly to the background esr of oxygen. (1) L. K. Keys, J . Phys. Chem., 70,3760 (1966). (2) A. F.Henry, Phys. Rev., 80,396 (1950). (3) M. Tinkham and M. W. P. Strandberg, ibid., 97, 937, 951 (1955). (4) A Carrington, D. H. Levy, and T. A. Miller, J . Phys. Chem., 71, 2372 (1967), (5) J. M.Hendrie and P. Kusch, Phys. Rev., 107,716 (1957). (6) K. D. Bowers, R. A. Kamper, and C. D. Lustig, Proc. Roy. Soe. (London), A251,565 (1959). (7) P. Cornaz, H. Choffat, M. Parot, and J.-P. Borel, “Physics of Non-Crystalline Solids,” J. A. Prins, Ed., Interscience Publishers, Inc., New York, N. Y., 1965,p 207.

MATERIAL^ RESEARCH LABORATORY PENNSYLVANIA STATEUNIVERSITY UNIVERSITY PARK, PENNSYLVANIA

L. K. KEYS

16802

RECEIVED APRIL7, 1967

Reply to “Comment on Electron Spin Resonance of

016-017,

017-01s, and O18-0l6”

by Carrington, Levy, and Miller

Sir: Recently we reported the observation of several

A Comment on the Steric Factor Approach to Translational-Vibrational Energy Transfer

low-field electron spin resonance peaks in gaseous 0 2 . l Sir: In many theoretical treatments2 of vibrational Based upon simple considerations of the vector model excitation of a diatomic molecule B-C colliding with of the atom,2 we have interpreted these as possible atom A (or one end of diatomic molecule A-D), the 016-017, 0’7-018, and 0l6-Ol8 absorption peaks. More initial relative A,B-C velocity vector VA, or an effective quantitative studies of these peaks have been carried V A , ~ is considered directed toward the B-C center of by Tinkham and Strandberg,3 who observed a large mass. Approximations2 are introduced so that the number (also subsequently observed by the author) in vibrational energy transfer to B-C averaged over e,4 this same field region. These esr peaks have been inthe angle between the B-C axis and VA, is obtained by terpreted as 0 l6-0l6transitions from considerations of multiplying the collinear (0 = 0) energy transfer value detailed calculations correcting for the various effects by a steric factor u less than unity.2 We show that as mentioned in the previous comm~nication.~ this steric factor approach cannot be generally correct. While these results seem to weaken the previous We have obtained exact numerical solutions to the interpretation’ of these lines, the disagreement between classical equations of motion, with A,B,C restricted to the various investigators apparently indicates, however, that the more quantitative treatment cannot be (1) Research performed under the auspices of the U. 9. Atomic rigorous.y applied. Hendrie and Kuschs have obEnergy Commission. tained from independent measurements at low(2) See, for instance: (a) K. Takanayagi, Progr. Theoret. Phys. S U P P L25,1 (1963); (b) K. F. Herzfeld and T.A. Litovitz, “Absorp field strengths by a molecular-beam method. These and Dispersion of Ultrasonic Waves,” Academic Press Inc., results are not in accord with those of ~ i ~ and k h tion ~ N. Y., 1959,Chapter 7 ; (0) K. F. Herzfeld and V. Griffing, New~York, J . Phys. Chem., 61,884 (1957); (d) C. B . Moore, J . C h a . Phys., 43, Strandberg. More recent studies by Bowers, et u Z . , ~ 2979 (1965). a repeat of the work of Tinkham and Strandberg, (3) Takanayagi (ref 2a) employs the quantum analog of an “effeoproduced results in disagreement with both of the t,ve in his MWN approx~ation. previous investigations. According to these results, (4) Or the appropriate quantum mechanical operation. vAp$

Volume 71, Number 7 Juns 1967