The double nuclear quadrupole splitting structure in 2-chloroacrylonitrile was resolved in spectra recorded with a supersonic beam, cavity Fourier transform microwave spectrometer. Splitting patterns in both a-and b-type transitions were analyzed, and perturbations arising from the proximity of the
Nuclear Quadrupole Coupling in 1,1,1-Trichloroethane: Inertial and Principal Tensors for35Cl and37Cl
✍ Scribed by L. Dore; Z. Kisiel
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 270 KB
- Volume
- 189
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The hyperfine structure in the J = 1 <-- 0 and J = 2 <-- 1 transitions of 35Cl3CCH3 and 35Cl237ClCCH3 was resolved by utilizing the sub-Doppler resolution of a pulsed supersonic beam, cavity Fourier transform microwave (FTMW) spectrometer. The complete inertial and principal quadrupole tensors of the chlorine nuclei are determined. The symmetric top treatment for 35Cl3CCH3 and the asymmetric top treatment for 35Cl237ClCCH3 are found to yield identical results for the principal tensor components of the 35Cl nucleus. The quadrupole asymmetry parameter eta for the chlorine nuclei in 1,1,1-trichloroethane is small, which indicates nearly cylindrical symmetry of the field gradient. Nevertheless, there is evidence for some deviation of the z symmetry axis of the field gradient from the direction of the C-Cl bond. Copyright 1998 Academic Press.
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The nuclear quadrupole hyperfine structure in rotational transitions of cis-1-chloro-2-fluoroethylene was measured for both 35 Cl and 37 Cl containing isotopomers in the millimeter-wave region. Near degeneracies of the 9 3,7 and 10 2,9 levels of 35 ClHCACFH and of the 19 9,10/11 and 17 10,7/8 levels
## Abstract One‐bond ^37^Cl/^35^Cl isotope effects on ^13^C NMR chemical shifts were used to assign the ^1^H and ^13^C NMR spectra of bis(4‐chlorophenyl)sulfone, 4,5‐dichlorophthalic acid and 2,2^′^‐thiobis(4,6‐dichlorophenol). The chlorine‐bonded carbons showed characteristic peaks separated by ab