## Abstract ^13^C chemical shifts obtained under uniform conditions for selected compounds containing secondary aliphatic fragments were employed in a linear regression analysis. Twoโparameter relationships describing the substituent effects in the saturated framework were calculated, and the usefu
Methyl substituent effects on the 13C chemical shifts at the carbenium center of 2-aryl-2-propyl cations
โ Scribed by David A. Forsyth; Robert M. Burk; Henry D. Babenco
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 234 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Methyl substituent effects on 13 c NM!? shifts of arylcarbenzwn zom are exannned as a probe of charge dzstnbution and are compared to methy effects on the solvoZyszs rates of I-a.ryZethyI derivatives. We have measured the effect of methyl substitution in the aromatic ring of 2-aryl-2-propyl cations, ArC(CH3j2+. on the 13 C NMR chemical shift of the carbenium center, C+. These data were obtained with the expectation that
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The "C NMR spectra of nine dichlorinated bicyclo[2.2.l]heptanes (norbornanes) have been measured and assigned. The pairwise effects of chlorine substituents which cause deviations from the additivity of single-snbstituent effects were investigated and are discussed. The largest effect found is the h
The 13C chemical shifts of 2-R-3-methylbenzothiazolium quaternary salts and the corresponding ZRbenzothiazoles are presented. ## KEY WORDS I3C NMR Substituent effects 2-R-3-methylbenzothiazoliurn quaternary salts 2-R-benzothiazoles reveal some systematic trends in the 13C data for these comr>ound
## Abstract The ^13^C NMR chemical shifts for 1,3โdithiolane and 13 methyl substituted derivatives are reported. Substituent effects are derived and compared with those for cyclopentanes and 1,3โdioxolanes. The magnitude and variety of the substituent effects are best explained with the aid of a ha