Abstract
The reaction of hexachlorodisilazanyllithium (Cl3Si)2NLi (1), with TiCl4 leads selectively to the novel fully chlorinated amides (Cl3Si)2NTiCl3 (2) or [(Cl3Si)2N]2 TiCl2 (3), respectively, depending on the molar ratio of the starting materials. The analogous reaction of 1 with WCl6 yielded the amide imide Cl3SiNW(Cl3)N(SiCl3)2 (5) by elimination of SiCl4. The relative amounts of the starting materials had no effect on the formation of 5. 14/15N- and 29Si-NMR data on the starting materials and products show significantly different effects, when compared with those of analogous N-trimethylsilyl derivatives, due to the lower energy of the electrons in the NSi and NM ß bonds. The crystal structure of 5 (triclinic, space group P1) was determined by X-ray structure analysis.
Item Type: | Journal article |
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Form of publication: | Publisher's Version |
Keywords: | N-Silyl amides; Precursor; 14N-NMR; Titanium; Tungsten |
Faculties: | Chemistry and Pharmacy |
Subjects: | 500 Science > 540 Chemistry |
URN: | urn:nbn:de:bvb:19-epub-14496-4 |
ISSN: | 0009-2940 |
Language: | English |
Item ID: | 14496 |
Date Deposited: | 30. Jan 2013, 14:30 |
Last Modified: | 04. Nov 2020, 12:54 |