Related Experiment Video
Updated: Mar 26, 2026

Fabrication and Optimization of Type II Silicon Clathrate Films
Published on: October 14, 2025
Isolation and Versatile Derivatization of an Unsaturated Anionic Silicon Cluster (Siliconoid)
Philipp Willmes1, Kinga Leszczyńska1, Yannic Heider1
1Krupp-Chair for General and Inorganic Chemistry, Saarland University, Am Markt, Zeile 1, 66123, Saarbrücken-Dudweiler, Germany.
Abstract:
The characteristic features of bulk silicon surfaces are echoed in the related partially substituted-and thus unsaturated-neutral silicon clusters (siliconoids). The incorporation of siliconoids into more-extended frameworks is promising owing to their unique electronic features, but further developments in this regard are limited by the notable absence of functionalized siliconoid derivatives until now. Herein we report the isolation and full characterization of the lithium salt of an anionic R5 Si6 -siliconoid, thus providing the missing link between silicon-based Zintl anions and siliconoid clusters. Proof-of-principle for the high potential of this species for the efficient transfer of the intact unsaturated R5 Si6 moiety is demonstrated by clean reactions with representative electrophiles of Groups 13, 14, and 15.
Related Concept Videos
α-Halogenation of Carboxylic Acid Derivatives: Overview
Electrophilic Addition to Alkynes: Hydrohalogenation
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Nucleophilic Aromatic Substitution: Elimination–Addition
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement

