ISSN:
0749-1581
Keywords:
High-resolution solid-state
;
13C NMR
;
Chemical shift non-equivalence
;
Methoxybenzenes
;
Phenols
;
meso-Hexestrols
;
Chemistry
;
Analytical Chemistry and Spectroscopy
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
13C NMR spectra of para-substituted methoxybenzenes and phenols were recorded in the solid state to gain an insight into the manner and origin of substantial peak splittings in the ortho (up to 9.2 ppm) and meta (up to 2.5 ppm) carbon signals. It was difficult to account for these peak splittings only by the steric interaction with the methyl group of the substituent, because their magnitude varied widely from 4.6 to 9.2 ppm with a variety of substituents at the para position, and the meta carbon peaks are also split into doublets. Instead, it was found that the electron density non-equivalence between the two ortho and the two meta carbons is mainly responsible for the splittings, as manifested by the presence of an approximate linear relationship between the displcements of the 13C NMR peaks and total electron density. The observed additional splitting in the 13C NMR spectra of meso-hexestrol and its methyl or ethyl ether(s) in the solid state was similarly explained. Stereochemical features of these molecules in the solid state are discussed on the basis of the 13C NMR data.
Additional Material:
6 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/mrc.1260260212
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