The book by Pihlaja and Kleinpeter is another addition to the well known VCH series on Methods in Stereochemical Analysis. Its backbone is made up by Chapters 4A, B and C and 5. Chapter 4A (77 pages, 88 references) is entitled 'Conformational and Configurational Analysis and Substituent Effects on
Carbon-13 and related NMR chemical shifts in alkylammonium and alkylphosphonium salts
โ Scribed by David J. Evans; G. Jeffery Leigh; Colin J. Macdonald
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 296 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The ^13^C NMR chemical shifts of the ฮฑโcarbon atoms in cations [NR~4~]^+^, [NR~3~CH~2~Ph]^+^ and [PR~4~]^+^ [R = Me, Et, Pr^n^, Bu^n^ or Pe^n^ (nโpentyl)] are found at anomalously high field in comparison with the corresponding shifts in RCl or RNH~2~. This is ascribed in part to the effect of the positive charge. The effect is detectable but less pronounced with ฮฒโcarbon atoms, but is not detectable in subsequent carbon atoms in longer alkyl chains.
๐ SIMILAR VOLUMES
The 13C NMR chemical shifts of nitriles and nitro compounds derived from nineteen aliphatic and seven aromatic systems have been recorded and assigned. The shifts are compared with those of the hydrocarbons to give the substituent effects of the CN and NO2 groups.
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15N, 1 7 0 and 33S N M R chemical shifts were determined for some aliphatic and aromatic sulphonamides, sulphinamides, sulphenamides and related sulphones and sulphoxides. The 1 7 0 and NMR chemical shifts change only slightly for the sulphonyl compounds. In the sulphinyl componnds, on the other han
## Abstract Carbonโ13 NMR chemical shifts (CDCl~3~ and C~6~D~6~ solvents) and relaxation times (__T__~1~) were determined for carbons in a series of allenic esters [RR~1~C๏ฃพC๏ฃพCHCO~2~ Et; (1) R = R~1~ = H; (2) R = H, R~1~ = CH~3~; (3) R = H, R~1~ = CH~3~CH~2~; (4) R = R~1~ = CH~3~; (5) R = CH~3~, R~1