The 13 C NMR spectra of copolymers of ethylene with 4-methyl-1-hexene and 4-methyl-1-pentene, respectively, were compared. The 4-methyl-1-hexene/ethylene copolymer, which contains an unsymmetric 2-methylbutyl branch, exhibits two distinct 13 C NMR peaks for each of the pairwise methylenes spaced one
The determination of the COOH substiuent effect for branched carboxylic acids from carbon-13 chemical shifts
✍ Scribed by David H. Marr
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 330 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The carboxyl substituent effects for branched carboxylic acids have been determined by carbon‐13 Fourier ransform nuclear magnetic resonance of eighteen measured and reported branched acids. For α‐branched systems the substituent effects are α = 15.3 ppm, β = 2.6 ppm, γ = −1.9 ppm, δ = 0.9 ppm and ϵ = 0.5 ppm. For other branched acids, the determined carboxyl substituent effects are α = 19.2 ppm, β = 2.1 ppm, γ = −1.4 ppm, δ = 0.6 ppm, and ϵ = 0.6 ppm.
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