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With Replacement of Two Fluoroalkoxy Groups

Heating tris[fluoroalkoxy] tellurium fluorides with 4-methylbenzenesulfonamide at 110°/0.04 torr caused fluoroalkoxy (4-methylbenzenesulfonimido) tellurium fluorides to form.  [Pg.98]


With Replacement of two Fluorine Atoms and two Fluoroalkoxy Groups... [Pg.101]

The first polyphosphazenes to be developed commercially were polymers with two different types of fluoroalkoxy side groups attached to the same chain.142 145a A typical example is shown in 3.73. Polymer 3.73 has a more complicated structure than is implied by the illustration. The polymer is synthesized by the reaction of a mixture of CF3CH2ONa and CFB CFj CHjONa with poly(dichlorophosphazene). This means that the two nucleophiles compete for replacement of the available chlorine atoms, a process that could lead to a random distribution of side groups, but could also generate repeating units in which the phosphorus atoms bear two of the same side groups. [Pg.112]

Fluoroalkoxy tellurium chlorides react with N-trimethylsilylmorpholine in diethyl ether at 5° with preferential replacement of fluoroalkoxy groups. Only two morpholino groups can be introduced into the molecules, even when an excess of the amine is used1. [Pg.105]


See other pages where With Replacement of Two Fluoroalkoxy Groups is mentioned: [Pg.98]    [Pg.100]    [Pg.98]    [Pg.100]    [Pg.98]    [Pg.100]    [Pg.98]    [Pg.100]    [Pg.260]    [Pg.8]   


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