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

M.G. Goesten, R. Hoffmann, F.M. Bickelhaupt, E.J.M. Hensen

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

10 Citaten (Scopus)
2 Downloads (Pure)


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 solid-state compounds.
Originele taal-2Engels
Pagina's (van-tot)828–833
Aantal pagina's6
TijdschriftProceedings of the National Academy of Sciences of the United States of America (PNAS)
Nummer van het tijdschrift5
StatusGepubliceerd - 2017


Duik in de onderzoeksthema's van 'Eight-coordinate fluoride in a silicate double-four-ring'. Samen vormen ze een unieke vingerafdruk.

Citeer dit