The thermal decomposition of [Me 2 Ga±N( i Bu)SnMe 3 ] 2 (prepared by the reaction of [Me 2 SnN i Bu] 3 with GaMe 3 in a 1 : 3 molar ratio) in an evacuated, sealed tube at 160 °C forms [MeGaN i Bu] 6 in high yield and SnMe 4 . Mass, 1 H and 13 C NMR as well as some IR and Raman spectroscopic data ar
Synthese, NMR-Spektren und Molekülstruktur von [(CH3)2Ga{μ-P(H)Si(CH3)3}2Ga(CH3)2{μ-P(Si(CH3)3)2}Ga(CH3)2]
✍ Scribed by A. Schaller; H.-D. Hausen †; J. Weidlein; P. Fischer
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- German
- Weight
- 82 KB
- Volume
- 626
- Category
- Article
- ISSN
- 0372-7874
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✦ Synopsis
The title compound has been prepared in good yield by the reaction of [Me 2 GaOMe] 3 (Me = CH 3 ) with HP(SiMe 3 ) 2 in toluene (ratio 1 : 1,1) and purified by crystallization from pentane or toluene, respectively. This organogallium compound forms (Ga±P) 3 ring skeletons with one Ga±P(SiMe 3 ) 2 ±Ga and two Ga±P(H)SiMe 3 ±Ga bridges and crystallizes in the monoclinic space group C2/c. The known homologous Al-compound is isotypic, both (M III ±P) 3 heterocycles have twist-conformations, the ligands of the monophosphane bridges have trans arrangements.
📜 SIMILAR VOLUMES
The synthesis, properties and X-ray single crystal structure bridges. In contrast, compounds 2 and 3a-b (R = CH 3 , C 2 H 5 ) are monomeric in the solid state. The suitability of the analysis of the intramolecularly adduct-stabilised organogallium bisazide (N 3 ) 2 Ga[(CH 2 ) 3 NMe 2 ] (1), the mono