Darstellung, Kristall- und Molekülstruktur eines zwölfgliedrigenN,N′-Di-Lithium-cyclosiloxazans [Me2SiOSiMe2N(Li)SiMe2O]2
Autor: | Michael Veith, Andreas Rammo, Volker Huch, Ralf Heim |
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Rok vydání: | 2010 |
Předmět: | |
Zdroj: | Zeitschrift für anorganische und allgemeine Chemie. 636:320-324 |
ISSN: | 1521-3749 0044-2313 |
DOI: | 10.1002/zaac.200900366 |
Popis: | The twelve membered and eighteen membered cyclosiloxazanes [Me2SiOSiMe2N(H)SiMe2O]2 (3) and [Me2SiOSiMe2N(H)SiMe2O]3 (4) have been obtained as colourless liquids from the reaction of 1,5-Dichlorohexamethyltrisiloxane with ammonia at–50 °C without any solvent. For compound 3 and 4, the yield is 30 % and 43 %, respectively. The treatment of 3 with two equivalents of n-butyllithium in n-hexane leads in almost quantitative yield (93 %) to the dilithiumsilylamide [Me2SiOSiMe2N(Li)SiMe2O]2 (5). Compound 5 can be isolated at room temperature and recrystallized from benzene without any decomposition or contraction of the ring size. An X-ray structure determination on [Me2SiOSiMe2N(Li)SiMe2O]2 (5) reveals a waved crown-like twelve membered Si6N2O4-cycle. Each of the two lithium ions is coordinated by two nitrogen and two oxygen atoms leading to a square pyramid, in which the metal occupies the apex. The two square-pyramidal coordination figures are located above and below the waved crown-like Si6N2O4-ring sharing a common edge by the atoms N(1) and N(2). All synthesised compounds have been characterised by spectroscopic methods. Because of the lower solubility of the dilithiumsilylamide 5, only a 1H-NMR could be applied for further characterisation in solution. |
Databáze: | OpenAIRE |
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