## Abstract An isotope effect of about 0·1 Hz at 25 MHz (0·004 ppm) on the ^13^C chemical shifts due to directly bonded chlorine has been observed at −50°C for hexachloropropene, hexachlorobutadiene and tetrachlorobutenyne. This effect yields an unambiguous assignment of ^13^C NMR lines to specific
35Cl/37Cl one-bond isotope effects on 13C chemical shifts in a series of para-substituted chlorobenzenes
✍ Scribed by Martha S. Morales-Ríos; Cirilo García-Martínez; Pedro Joseph-Nathan; L. Gerardo Zepeda
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 229 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
One‐bond isotope shifts of ^35^Cl/^37^Cl natural abundance chlorine isotopomers were measured in the 75.4 MHz ^13^C NMR spectra of a series of para‐substituted chlorobenzenes. The high‐field isotope shift effect ^1^Δ^13^C(^37^Cl) was established from the relationship between the chlorine isotopomeric ratio and the carbon peak intensities. It was found that the ^1^Δ^13^C(^37^Cl) values are in the range of −4.0 to −5.2 ppb. The isotope shifts tend to decrease as the electron‐attracting character of the substituent increases, providing a linear correlation between the isotope shift and the chemical shift of the chlorine‐bearing carbon.
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