Report

Characterization of hydrogen-substituted silylium ions in the condensed phase

See allHide authors and affiliations

Science  12 Jul 2019:
Vol. 365, Issue 6449, pp. 168-172
DOI: 10.1126/science.aax9184

You are currently viewing the editor's summary.

View Full Text

Log in to view the full text

Log in through your institution

Log in through your institution

An acidic route to silicon cations

The simplest silicon cation, with a central Si atom bonded to just three hydrogens, has long eluded bulk synthesis. Wu et al. now report a straightforward route to this molecule by reacting a carborane acid with phenyl silane, producing benzene and the silylium carborane ion pair. A similar protocol offered efficient syntheses of primary and secondary silyl cations through acidic cleavage of Si–phenyl or Si–H bonds. All three products, characterized crystallographically and in solution, manifested weak coordination to bromine substituents of the carboranes.

Science, this issue p. 168