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Hexacoordinate germanium complexes

The formation of organic derivatives of penta- and hexacoordinate germanium is due to a later time when the reactions of organohalogermanes were studied with ammonia and amines (see Section ILF). When these reactions were conducted at low temperatures, 1 1 and 1 2 adducts were formed. When heated >0 °C, the complexes of organohalogermanes with ammonia, primary and secondary amines decomposed to give compounds... [Pg.31]

Quite recently, it was established that the formation of the pentacoordinated germanium and tin compounds EF4(CH2CH=CH2) from EF3(CH2CH=CH2) (E = Ge, Sn) by the addition of F is exothermic148. The nucleophilicity of the allylic y-carbon is much enhanced when the pentacoordinated EF4(CH2CH=CH2) is formed. These results are qualitatively similar to those found for the reaction of the corresponding silicon compound. The pentacoordinated Ge and Sn complexes have a significant Lewis acidity which allows them to form stable hexacoordinated intermediates in the course of the reaction. [Pg.575]

Hypervalent compounds of organic germanium, tin and lead derivatives 1149 IX. HEXACOORDINATE ANIONIC COMPOUNDS A. Intermolecular Complexes... [Pg.1149]


See other pages where Hexacoordinate germanium complexes is mentioned: [Pg.569]    [Pg.1015]    [Pg.175]    [Pg.112]    [Pg.569]    [Pg.1015]    [Pg.175]    [Pg.112]    [Pg.569]    [Pg.1156]    [Pg.1015]    [Pg.1156]    [Pg.287]    [Pg.466]    [Pg.985]    [Pg.1148]    [Pg.1158]    [Pg.466]    [Pg.985]    [Pg.1148]    [Pg.1158]    [Pg.133]    [Pg.78]   


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Germanium complexes

Hexacoordinate complexes

Hexacoordination

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