## Abstract The ^13^C^13^C spin–spin coupling constants in natural abundance oxetane, thietane, cyclobutanone, bromo‐and chlorocyclobutane have been measured. Furthermore, the ^13^C isotope‐induced changes in the chemical shifts of the different ^13^C nuclei in the molecules mentioned above are re
Isotope effects on the 13C chemical shift and carbon–proton coupling constant in dichloromethane
✍ Scribed by N. M. Sergeyev; N. D. Sergeyeva; W. T. Raynes
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 489 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Carbon–proton and carbon–deuteron coupling constants were measured in the isotopomers CH~2~Cl~2~, CHDCl~2~ and CD~2~Cl~2~. The primary and secondary isotope effects on the carbon–proton coupling are −0.60 (±0.05) and −0.25 (±0.01) Hz, respectively. The deuterium‐induced ^13^C isotope shifts proved to be almost linearly dependent on the number of deuterium atoms, although there is a small but significant non‐additivity.
📜 SIMILAR VOLUMES
## Abstract Long range inter‐ring ^13^C^13^C couplings are found to be effective in the title compounds, and the magnitudes of coupling constants and of substituent effects on ^13^C chemical shifts, as well as the signs of the latter, alternate with respect to the number of connecting bonds.
## Abstract The effects of an hydroxy substituent on ^13^C^13^C coupling constants and ^13^C chemical shifts have been measured in 1‐hydroxynaphthalene‐2‐^13^C and 1‐hydroxypyrene‐1‐^13^C. The changes observed in the ^13^C^13^C couplings show the effect of a substituent attached directly to the l
Primary p\*J(13C,H) and secondary s\*J(13C,H) isotope e †ects on carbonÈproton coupling constants were measured in studies of proton-and deuteron-coupled 13C NMR spectra of the halomethanes CH n D m X 4~n~m , where X is Cl, Br or I. Both e †ects are always negative. The magnitudes of p\*J(13C,H) inc
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