Synthesis of a cyclopentadienyl(imino)stannylene and its direct conversion into halo(imino)stannylenes

18Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

The reaction of stannocene Cp2Sn with iminolithium LiNIPr (NIPr = bis(2,6-diisopropylphenyl)imidazolin-2-iminato) afforded the dimeric cyclopentadienyl(imino)stannylene [(η1-Cp)SnNIPr]2 (1). Compound 1 exhibits unexpected reactivity towards haloalkanes. The high-yield conversion of 1 into chlorostannylene [ClSnNIPr]2 (2) and bromostannylene [BrSnNIPr]2 (3) were accomplished by treatment with dichloromethane or 1,2-dibromoethane, respectively, through a Cp-substitution reaction.

Cite

CITATION STYLE

APA

Ochiai, T., & Inoue, S. (2017). Synthesis of a cyclopentadienyl(imino)stannylene and its direct conversion into halo(imino)stannylenes. RSC Advances, 7(2), 801–804. https://doi.org/10.1039/c6ra27697k

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free