The NMR spectrum and conformation of 2,3-difluoropropionic acid ethyl ester
✍ Scribed by G. Hägele; R. K. Harris; P. Sartori
- Book ID
- 102950612
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- English
- Weight
- 541 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 'H and ISF NMR spectra of the CH,FCHF group in FCH,CHFCO,C,H, were analysed on the basis of an ABCXY spin system. The non-equivalence of the methylene protons is discussed in terms of rotational isomerism. It is concluded that the dominant rotamer is probably considerably distorted from a perfectly staggered orientation. The variation of 3JI.rE with substituent electronegativity is reviewed.
📜 SIMILAR VOLUMES
Rotationally resolved fluorescence excitation spectra of the S~ ~-S o origin bands of two conformers of methyl-3-aminobenzoate and four conformers of ethyl-3-aminobenzoate have been obtained. Analyses of these spectra yield the rotational constants of each conformer in the two electronic states and
## Abstract The assignment of lines in the ^13^C NMR spectrum of abietic acid and its methyl ester have been made using carbon __T__~1~ values and lanthanide induced shift effects. Structure–NMR parameter values are briefly discussed.
## Synopsis C Z ~H : ~~N ~O ~, orthorhombic, B212121; a = 39.432 (lo), b = 14.061 ( 5 ) , c = 4.850 (2) A, M = 494 a.m.u., Z = 4, Dm = 1.22 g cm-:', Dr = 1.22 g cm-3, R = 0.13 for 1205 observed reflections alter refinement with isotropic thermal factors. The urethane and amide bonds are in the tra