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Organoantimony homocycles

TABLE 9. Colours and structural data of some associated organoantimony homocycles... [Pg.451]

This observation sheds some light on the question as to why pentamers are formed with n-alkyl substituents but hexamers with slim aryl substituents. A possible explanation, at least for the organoantimony homocycles, is that in solution jjentamers dominate both with alkyl and aryl substituents. In the solid state, however, the six-membered form allows a closer packing of the phenylantimony rings than the pentameric form. [Pg.568]


See other pages where Organoantimony homocycles is mentioned: [Pg.63]    [Pg.441]    [Pg.441]    [Pg.451]    [Pg.451]    [Pg.563]    [Pg.565]    [Pg.567]    [Pg.569]    [Pg.571]    [Pg.573]    [Pg.574]    [Pg.575]    [Pg.578]    [Pg.441]    [Pg.441]    [Pg.451]    [Pg.451]    [Pg.451]    [Pg.565]    [Pg.567]    [Pg.569]    [Pg.571]    [Pg.573]    [Pg.574]    [Pg.575]    [Pg.578]    [Pg.1011]   


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