Trimethylsilyl and tert-butyldimethylsilyl derivatives of naturally occurring purines and pyrimidines and also other closely related model compounds were prepared and their 29Si NMR spectra measured. Only the chemical shifts of the SiÈNHÈ moiety could be assigned experimentally (i.e. exactly) ; the
29Si NMR spectra of tert-butyldimethylsilylated alcohols
✍ Scribed by Jan Schraml; Magdalena Kvíčalová; Vratislav Blechta; Jan Čermák
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 223 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
29Si NMR spectra of a series of tert-butyldimethylsilyl derivatives of simple alcohols were measured under standard conditions in chloroform-d. The chemical shifts are linearly related to those in analogous trimethylsilyl derivatives. The correlation is very good (r = 0.998, n = 24) but signiÐcantly di †erent from the correlation which holds for derivatives of amino acids (including both SiÈN and SiÈO silicon atoms) despite that the two correlations cover approximately the same range of chemical shifts. The quality of the correlation now reported (error estimate » 0.19 ppm) is such that it should allow the detection of speciÐc interactions that might occur in the case of silylated polyols. The observed chemical shifts are a †ected by polar e †ects and by sterically controlled association with the solvent (chloroform), but other factors are not excluded. 1997
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