Reactivity of cationic molybdenum(II) complexes. Part 3. Synthesis of methoxide and carbomethoxide derivatives of η-pentamethylcyclopentadienyl–molybdenum(II) and the crystal structure determination of the oxidation product trans-[{Mo(η-C5Me5)(O)2}2(µ-O)]

Author(s):  
Piero Leoni ◽  
Marco Pasquali ◽  
Liana Salsini ◽  
Cristina di Bugno ◽  
Dario Braga ◽  
...  
1985 ◽  
Vol 40 (8) ◽  
pp. 1023-1028 ◽  
Author(s):  
Uwe Klingebiel ◽  
Sabine Pohlmann ◽  
Lutz Skoda ◽  
Cornelia Lensch ◽  
George M. Sheldrick

AbstractThe nature of the products which are formed in the reaction of tris(trimethylsilyl)Methylfluorosilanes (Me3Si)3C -SiF2R with KOH depends on the bulkiness of the substituents R. The condensed siloxane is obtained for R = F . The crystal structure determination of this siloxane (Me3Si)3C -SiF2-O -SiF2-C (SiMe3)3 shows that the Si -O - Si unit is linear. A fluorosilanol as well as a siloxane could be isolated for R = Me. 1,3-Migration of one or two trimethylsilyl groups from the carbon to the oxygen takes place for R = phenyl, rm-butyl or silylamine, with formation of siloxanes which are isomeres o f the expected silanols.


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