Eight-coordinate fluoride in a silicate double-four-ring

Maarten G. Goesten, Roald Hoffmann, F. Matthias Bickelhaupt, Emiel J.M. Hensen

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Fluoride, nature's smallest anion, is capable of covalently coordinating to eight silicon atoms. The setting is a simple and common motif in zeolite chemistry: the box-shaped silicate double-four-ring (D4R). Fluoride seeks its center. It is the strain of box deformation that keeps fluoride in the middle of the box, and freezes what would be a transition state in its absence. Hypervalent bonding ensues. Fluoride's compactness works to its advantage in stabilizing the cage; chloride, bromide, and iodide do not bring about stabilization due to greater steric repulsion with the box frame. The combination of strain and hypervalent bonding, and the way they work in concert to yield this unusual case of multiple hypervalence, has potential for extension to a broader range of solidstate compounds.

Original languageEnglish
Pages (from-to)828-833
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume114
Issue number5
DOIs
Publication statusPublished - 31 Jan 2017
Externally publishedYes

Keywords

  • Chemical bonding
  • Hypervalence
  • Main-group chemistry
  • Zeolite chemistry

ASJC Scopus subject areas

  • Multidisciplinary

Fingerprint

Dive into the research topics of 'Eight-coordinate fluoride in a silicate double-four-ring'. Together they form a unique fingerprint.

Cite this