2000
DOI: 10.1002/1521-3935(20000901)201:14<1742::aid-macp1742>3.0.co;2-h
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Syntheses of poly[(dimethyl)-co-(4,7,10,13-tetraoxatetradecylmethylsilanes)].An evaluation of the use of C8K versus Na in the preparation of polysilanes

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Cited by 10 publications
(13 citation statements)
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“…A similar observation raised from 13 C NMR analysis, which showed signals corresponding to the presence of THF (w27 and 70 ppm) and ring opening products (w16, 20, 30 and 64 ppm). 29 Si NMR exhibited signals between 12 and À86 ppm, which were assigned to silicon atoms bonded with 3 to 0 Cl atoms, respectively [33,34]. Elemental analysis led to the following stoichiometry Si 1 Cl 1.53 C 2.26 H 4.69 in agreement with the presence of organic residues formed by reaction with THF (calculated Si 1 Cl 0.12 ).…”
Section: Resultsmentioning
confidence: 95%
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“…A similar observation raised from 13 C NMR analysis, which showed signals corresponding to the presence of THF (w27 and 70 ppm) and ring opening products (w16, 20, 30 and 64 ppm). 29 Si NMR exhibited signals between 12 and À86 ppm, which were assigned to silicon atoms bonded with 3 to 0 Cl atoms, respectively [33,34]. Elemental analysis led to the following stoichiometry Si 1 Cl 1.53 C 2.26 H 4.69 in agreement with the presence of organic residues formed by reaction with THF (calculated Si 1 Cl 0.12 ).…”
Section: Resultsmentioning
confidence: 95%
“…However, as for M0, several peaks attributed to compounds formed by side reaction with THF were still observed. The solid-state 29 Si NMR exhibited several signals in the region from 20 to À90 ppm. There are very few examples of Si-np 29 Si NMR studies [15,35].…”
Section: Resultsmentioning
confidence: 99%
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