Double-resonance study of spin relaxation in two spin systems (AB) coupled to a quadrupolar nucleus
- 1 January 1970
- journal article
- research article
- Published by Taylor & Francis in Molecular Physics
- Vol. 18 (1) , 11-29
- https://doi.org/10.1080/00268977000100021
Abstract
A frequency sweep proton-proton double-resonance study of spin relaxation is made in strongly coupled two spin systems (AB) formed by the protons in 2-bromothiazole (sample I) and in 2,3,4-trichloronitrobenzene (sample II). The single-resonance transitions of both these molecules exhibit broadening due to scalar coupling with nearby 14N nuclei modulated by the rapid quadrupolar relaxation of the latter. A density-matrix analysis of double-resonance spectra obtained over a wide range of irradiation strengths coupled with a determination of 14N resonance linewidths and approximate measurements of proton relaxation times leads to a determination of the spin-spin coupling constants of 14N with the two protons, and the parameters describing the other mechanisms of proton relaxation in these molecules. It has been shown that a study of relaxation by double resonance is, in general, capable of yielding the relative signs of the coupling constants involving the 14N nucleus. The results obtained may be summarized as follows: Sample I (2-bromothiazole, neat liquid). (a) Single resonance: (b) Scalar coupling with 14N: J AN ≈ 9·7 hz and J BN ≈ 2·9 hz. J AN and J BN are of same sign. τq (relaxation time (T 1 or T 2) of 14N) = 0·61 ms. (c) The other important mechanism of proton relaxation is internal dipole-dipole interaction, with τ c = 7·0 × 10-12 s. Sample II (40 per cent solution of 2,3,4-trichloronitrobenzene in CS2). (a) Single resonance: J AB = 8·85 ± 0·1 hz, |v A - v B| = 11·3 ± 0·1 hz. (b) Scalar coupling with 14N: J AN ≈ 3·0 hz, J BN ≈ 0·4 hz. Unambiguous determination of relative signs of J AN and J BN was not possible since J BN is small. τq (14N) = 1·88 ms. (c) The other important mechanism of relaxation is internal dipole-dipole interaction with τ e = 1·0 × 10-10 s. Dipolar interaction with 14N or with any of the chlorine nuclei, scalar coupling with the chlorine nuclei and intermolecular dipolar interactions, do not make significant contributions.Keywords
This publication has 17 references indexed in Scilit:
- Nuclear relaxation and molecular properties Part I.14N nuclear quadrupolar relaxation and1H line shapes in nitrogen-containing heterocyclesMolecular Physics, 1968
- Relaxation effects in the nuclear magnetic double resonance spectra of a symmetrical three spin system (AB2)Molecular Physics, 1968
- Relaxation Effects in Nuclear Magnetic Double ResonancePhysical Review B, 1965
- The Principles of Nuclear MagnetismAmerican Journal of Physics, 1961
- The effect of quadrupole relaxation on nuclear magnetic resonance multipletsMolecular Physics, 1958
- A contribution to the theory of the exchange narrowing of spectral linesMolecular Physics, 1958
- On the Theory of Relaxation ProcessesIBM Journal of Research and Development, 1957
- Nuclear Magnetic Interactions in the HF MoleculeThe Journal of Chemical Physics, 1956
- Dynamical Theory of Nuclear Induction. IIPhysical Review B, 1956
- A Mathematical Model for the Narrowing of Spectral Lines by Exchange or MotionJournal of the Physics Society Japan, 1954