We have calculated the 29Si NMR shielding for the chlorosilanes, SiHXC14\_X, using both the coupled Hartree-Fock method and the random phase approximation localized-orbital local-origins method, obtaining trends in good agreement with experiment for the first part of the series. Calculated inner-she
Origin of the shielding effect in the 29Si NMR spectra of silatranes
✍ Scribed by V. F. Sidorkin; V. A. Pestunovich; M. G. Voronkov
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 417 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The diamagnetic and paramagnetic terms of the "Si nuclear shielding constant of silatranes, XSi(OCH2CHz)& and the related four-coordinated silicon compounds, triethoxysilanes, XSi(OC2H5),, have been estimated to explain the experimental peculiarities of their 29Si NMR spectra. High-field shifts of the %i NMR signals of silatranes relative to triethoxysilanes are of diamagnetic origin, arising mainly from the existence of the S i c N bond and pentamordination of the silicon atom in silatranes. At the same time, the decrease in the positive charge on the silicon atom upon S i c N interaction increases the absolute value of the negative paramagnetic term. When the Sic-N bond in silatrane molecules becomes stronger through introduction of a more electronegative substituent X, the absolute value of the difierence in the paramagnetic terms between silatranes and the related triethoxysganes increases to a greater extent than that in the diamagnetic terms. 'fhis reduces the difference in 29Si chemical shifts of the corresponding four-and five-coordinated silicon compounds with increasing electronegativity of the substituent X.
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## Abstract ^29^Si^1^H coupling constants across two and three bonds in silatranes and model triethoxysilanes were measured from ^1^H spectra by multiple quantum NMR. There was an increase in the ^29^SiOCH coupling in the equatorial position and a decrease in that in the axial position of the s