Issue 41, 2018

Generation of stannabenzenes and their monomer–dimer equilibration

Abstract

Stannabenzene has not been isolated so far because of its high reactivity. In order to synthesize and isolate a stable stannabenzene, we have introduced two steric protection groups, the Tbt (2,4,6-tris[bis(trimethylsilyl)methyl]phenyl) or the Bbt (2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl) group on the tin atom and the t-butyl group on the 2-position, to the stannabenzene skeleton. Such a combination of steric protection groups was found to suppress the dimerization of stannabenzene to some extent, giving an equilibrated mixture of the corresponding stannabenzene and its dimer.

Graphical abstract: Generation of stannabenzenes and their monomer–dimer equilibration

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2018
Accepted
27 Jul 2018
First published
31 Jul 2018

Dalton Trans., 2018,47, 14436-14444

Generation of stannabenzenes and their monomer–dimer equilibration

Y. Mizuhata, S. Fujimori, N. Noda, S. Kanesato and N. Tokitoh, Dalton Trans., 2018, 47, 14436 DOI: 10.1039/C8DT02994F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements