Geminal H,D spin-spin coupling and isotope effects in partially deuterated methyl-aromatic compounds
CG Macdonald, JS Shannon, Sever Sternhell
Abstract
CG Macdonald, JS Shannon, Sever Sternhell
Abstract
Seventeen methyl-aromatic compounds were selectively, partially deuterated by catalytic hydrogen exchange. The proton magnetic resonance (p.m.r.) spectra of the partially deuterated compounds showed that the geminal H,D coupling constant is approximately 2.2 c/s and that it does not vary significantly with the type of substitution in the ring. The deuterium isotope effect on the chemical shift of the remaining protons in the methyl group is approximately 0.7-1.1 c/s in the upfield direction for the introduction of one deuterium atom.
OpenAlex reports 13 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Seventeen methyl-aromatic compounds were selectively, partially deuterated by catalytic hydrogen exchange. The proton magnetic resonance (p.m.r.) spectra of the partially deuterated compounds showed that the geminal H,D coupling constant is approximately 2.2 c/s and that it does not vary significantly with the type of substitution in the ring. The deuterium isotope effect on the chemical shift of the remaining protons in the methyl group is approximately 0.7-1.1 c/s in the upfield direction for the introduction of one deuterium atom.
Key concepts: Geminal, Deuterium, Chemistry, Kinetic isotope effect, Methyl group, Ring (chemistry), Biocatalysis, Proton