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Silicon compounds, heteroatom nonbonding

It has been known for some time that the basicities of a heteroatom decrease upon a-silyl substitution [12], For example, alkyl silyl ethers (R3Si-0-R ) are less basic than dialkly ethers. Silylamines are weak bases compared to alkylam-ines. This electron-withdrawing effect of silyl groups has been explained in terms of the interaction between low lying vacant orbitals such as 3d orbitals of silicon or a orbitals with the nonbonding p orbitals (lone pairs) of the heteroatom (Fig. 4). This interaction decreases the HOMO level which in turn lowers the basicity of the heteroatom. Such effect may also cause the increase of the oxidation potentials, but little study has been reported on the electrochemical properties of this type of compounds. [Pg.54]


See other pages where Silicon compounds, heteroatom nonbonding is mentioned: [Pg.55]    [Pg.185]    [Pg.237]    [Pg.46]    [Pg.389]    [Pg.389]   


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