| | 2 | Author
| P. Jutzi, C. Batz, A. Mutluay | Requires cookie* | | | Title
| Eightfold Functionalization of the Octasilsesquioxane Core  | | | | Abstract
| Eightfold functionalized octasilsesquioxanes (R8Si80 12) are synthesized using the hydro silylation method. D ifferent types of groups R, consisting of an (-0 -S i M e 2(CH 2)2) spacer unit and various terminal units (-C H 2(C2M e)B 1oH1o, -C 5H 3M eM n(CO)3, -S iM e2C5H 4FeC5H 5 , -S iM e2Cl, -SiM eC l2, -S i(O E t)3) have been introduced. The hydro silylation products have been characterized by 'H, 13C, 29Si NMR and infrared spectroscopy and elemental analysis. The redox properties of the ferrocenyl substituted compound have been studied by cyclovoltammetry. Results | | | |
Reference
| Z. Naturforsch. 49b, 1689—1692 (1994); received May 17 1994 | | | |
Published
| 1994 | | | |
Keywords
| Octasilsesquioxanes, Hydrosilylation, Siloxanes, Ferrocenes, Carboranes | | | |
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| default:Reihe_B/49/ZNB-1994-49b-1689.pdf | | | | Identifier
| ZNB-1994-49b-1689 | | | | Volume
| 49 | |
| 3 | Author
| ChlorotrimethylsilaneJan Schneider3, Eckhard Popowski, Hans Fuhrmannb | Requires cookie* | | | Title
| Reaktionen von Lithiumhydridosilylamiden mit Carbonylverbindungen und Gemischen von Carbonylverbindungen und Chlortrimethylsilan Reactions of Lithium Hydridosilylamides with Carbonyl Compounds and Mixtures of Carbonyl Compounds | | | | Abstract
| The lithium hydridosilylamides Me2(H)SiN(Li)R (1: R = CM e3, 2: R = SiMe3) were allowed to react either with the non-enolizable carbonyl compounds CH2=C(Me)CHO, PhCHO and Ph2CO followed by trapping with chlorotrimethylsilane (A), or with mixtures of these carbonyl compounds and chlorotrimethylsilane (B). In the second case the course of the reactions is determined by the carbonyl compound. The composition of the reaction mixtures is nearly the same according to A and B. Main products in the reactions with the aldehydes are the corresponding imines R'CH=NR (R' = CH2=C(Me), Ph) 3 , 4 , 8 ,9 formed by addition of the hydridosilylamides to the C = 0 group of the aldehydes and subsequent LiOSiM e2H elimination. Partial hydrosilylation of the alde hydes by the hydridosilanolate followed by the trimethylsilylation yields the alkoxydisiloxanes R'CH2OSiMe2OSiMe3 6 , 11. In some cases 2 partially reacts under hydrosilylation to give the alkoxydisilazanes R'CH2OSiM e2NHSiM e3 7,12. The hydrosilylation is the preferred reaction of 1 and 2 with benzophenone. The compounds Ph2CHOSiMe2NHR 13, 14 are obtained. This difference in the reaction behaviour of 1 and 2 towards the aldehydes and benzophenone is mainly due to steric reasons. Depending on the conditions the imines Ph2C=NR 20, 21 may be formed. Ph2CHOSiM e2OSiMe3 (22) is a secondary product of imine formation. In all reactions of 1 and 2 with the carbonyl compounds the corresponding alkoxysilanes R'CH2OSiMe3 (5: R' = CH 2=C(Me), 6 : R' = Ph) and Ph2CHOSiM e3 (15) are generated. Compounds resulting from a reaction of 1 and 2 with chlorotrimethylsilane are produced to minor extent, but only if the molar ratio of amide to carbonyl compounds is not greater than one. The formation of a silanimine intermediate in reaction according to B is not observed. | | | |
Reference
| Z. Naturforsch. 53b, 663—672 (1998); eingegangen am 9. April 1998 | | | |
Published
| 1998 | | | |
Keywords
| Hydridosilylamides, Reaction Behaviour, Imines, Hydrosilylation | | | |
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| default:Reihe_B/53/ZNB-1998-53b-0663.pdf | | | | Identifier
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| 53 | |
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