Controlling Oxidative Addition and Reductive Elimination at Tin(I) via Hemi-Lability.

Caise A, Crumpton AE, Vasko P, Hicks J, McManus C, Rees NH, Aldridge S

We report on the synthesis of a distannyne supported by a pincer ligand bearing pendant amine donors that is capable of reversibly activating E-H bonds at one or both of the tin centres through dissociation of the hemi-labile N-Sn donor/acceptor interactions. This chemistry can be exploited to sequentially (and reversibly) assemble mixed-valence chains of tin atoms of the type ArSn{Sn(Ar)H}n SnAr (n=1, 2). The experimentally observed (decreasing) propensity towards chain growth with increasing chain length can be rationalized both thermodynamically and kinetically by the electron- withdrawing properties of the -Sn(Ar)H- backbone units generated via oxidative addition.