Issue 9, 1992

Structures and fragmentations of organosilicon and organotin radical cations

Abstract

EPR spectroscopy has been used to study radical cations derived from organosilicon and organotin compounds, as isolated in solid trichlorofluoromethane matrices at low temperatures. For the organotin radical cations depletion of electron density occurs from a unique C–Sn bond, and leads to dissociation on annealing for allyl- and benzyl-tin species, yielding allyl and benzyl radicals, respectively: remarkably, the dissociation is reversible for p-MeOC6H4CH2SnBu3˙+ radical cations. No such fragmentation is observed for the corresponding organosilicon species, even on annealing to the melting point of the matrix (ca. 160 K) despite evidence that the C–Si bonds are similarly depleted on ionisation. The Me2N(CH2)3SnBu3˙+ radical cation is unstable at 77 K, and fragments to form butyl radicals as the only detectable paramagnetic species.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1992, 1469-1474

Structures and fragmentations of organosilicon and organotin radical cations

E. Butcher, C. J. Rhodes, M. Standing, R. S. Davidson and R. Bowser, J. Chem. Soc., Perkin Trans. 2, 1992, 1469 DOI: 10.1039/P29920001469

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.

Spotlight

Advertisements