## Abstract Selected model carboxylic acids and esters dissolved in deuteriochloroform have been studied by carbon‐13 nuclear magnetic resonance under standardized conditions. Assignments of the chemical shifts have been made for all samples, and the spin–lattice relaxation times and nuclear Overha
Carbon-13 NMR spectra of adamantane carboxylic acids and diamantane mono- and di-carboxylic acids and esters
✍ Scribed by Milan Hájek; LuděK Vodička; Petr Trška; Vladimír Sklenář
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 257 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Table 4. Predicted and observed" aryl carbon shieldings relative to benzene for the 4-substituted phenylsulphonyl moiety in cis-and trans-l-arylsulphonyl-2-~lcy~opropanes shielding (pprn) Compound cis trans No. C-1' C-2 and C-6' C-3' and C-5' C-4' C-1' C-2 and C 6 ' C-3' and C-5' C-4' Carbon-13 NMR Spectra of Adamantane Carboxylic Acids and Diamantane Mono-and Di-carboxylic Acids and Esters The 13C NMR chemical shifts of 17 adamantane and diamantane mono-and dicarboxylic acids and methyl esters have been measured in CDCI, and D,O. The assignment of the chemical shifts was verified using an additivity rule and the lanthanide shift technique.
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