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Digermane, hexaphenyl

Digermane, hexaphenyl-, 6 72, 73 formation of, from triphenyl-germane and phenyllithium, 5 78... [Pg.233]

The following procedure, using tetrahydrofuran as solvent, is simpler and gives a higher yield of product (85%) than earlier methods. Complete removal of excess magnesium is essential to avoid the formation of hexaphenyl-digermane as a by-product. [Pg.31]

See also in sourсe #XX -- [ Pg.6 , Pg.8 , Pg.31 , Pg.72 , Pg.78 ]

See also in sourсe #XX -- [ Pg.6 , Pg.8 , Pg.31 , Pg.72 , Pg.78 ]

See also in sourсe #XX -- [ Pg.6 , Pg.8 , Pg.31 , Pg.72 , Pg.78 ]

See also in sourсe #XX -- [ Pg.6 , Pg.72 , Pg.73 ]

See also in sourсe #XX -- [ Pg.5 , Pg.8 , Pg.31 , Pg.72 , Pg.78 ]



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Digermanates

Digermane

Digermanes

Hexaphenyl

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