Abstract
Reactions of bis(triphenylmethyl)ytterbium and bis(triphenylgermyl)ytterbium with mercuric chloride, triphenylbismuth, iodine, tert-butyl alcohol, phenylacetylene, and cyclopentadiene were studied. The higher reactivity of the former compound in these reactions is explained by that the chemical bond in it is ionic, whereas in its germyl analog, covalent.
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