
Journal of Organometallic Chemistry p. 299 - 311 (1982)
Update date:2022-08-04
Topics:
Kobayashi, Kazuko
Kawanisi, Mituyosi
Hitomi, Torazo
Kozima, Sinpei
The fast decomposition of trialkylstannyllithiums, R3SnLi (R=Me, Et and Bu), in the presence of hexaalkyldistannanes, R3SnSnR3, was observed, and its mechanism was investigated kinetically.Partial dissociation of R3SnLi into a a solvent cage is suggested to occur in the initial step.The RLi in the complex can be trapped instantaneously by R3SnSnR3 to afford R4Sn and R3SnLi, and the counterpart R2Sn: by R3SnLi giving R3SnR2SnLi.The decomposition of R3SnLi followed first-order kinetics within 3.5 h, corresponding well to the rate of disappearance of R3SnSnR3 and of appearance of R4Sn.The partial dissociation rate constant (k1) of Me3SnLi into the complex was determined as 2.0*10-3 min-1.The values of k1 are about 100 times those of rate constants (k') for decomposition of R3SnLi in the absence of R3SnSnR3.Reformation of R3SnLi from the
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