Konrad W. Hellmann, Lutz H. Gade, Roland Fleischer and Dietmar Stalke
The crystal structure of the difunctional thallium(I) amide CH2 [CH2N(Tl)SiMe3]2 1 reveals a pattern of aggregation based on weak attractive metal–metal interactions, a situation which appears to be influenced by the degree of exposure of the thallium centres; this is evidenced by the solid-state structure of the more shielded analogue CH2[CH2N(Tl)SiButMe2]2 2 which features no significant Tl···Tl contacts.