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Hypervalent molecules are one of the exceptions to the octet rule. Bonding in most hypervalent molecules is well rationalized by the Rundle-Pimentel model (three-center four-electron bond), and high ionic bonding between the ligands and the central atom is essential for stabilizing hypervalent molecules. Here, we produced one of the simplest hypervalent anions, HF, which is known to deviate from the Rundle-Pimentel model, and identified its ro-vibrational features. High-level ab inito calculations reveal that its bond dissociation energy is comparable to that of dihalides, as supported by secondary photolysis experiments with irradiation at various wavelengths. The charge distribution analysis suggested that the F atom of HF is negative and hypervalent and the bonding is more covalent than ionic.
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http://dx.doi.org/10.1038/s41598-017-02687-z | DOI Listing |
Acc Chem Res
August 2025
Laboratory of Catalysis and Organic Synthesis, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LCSO, BCH 4306, 1015 Lausanne, Switzerland.
ConspectusAlkynes are one of the most fundamental functional groups in organic synthesis due to the versatile chemistry of the triple bond, their unique rigid structure, and their use in bioconjugation. The introduction of alkynes onto organic molecules traditionally relies on nucleophilic activation, often requiring strong bases or metal catalysts. These conditions, however, restrict applications involving biomolecules such as peptides and proteins due to functional group incompatibility.
View Article and Find Full Text PDFRSC Adv
August 2025
Department of Chemistry, Faculty of Science, Umm Al-Qura University Makkah 21955 Saudi Arabia
Interactions of hypervalent IF and XeFO molecules within the square pyramidal geometry σ-hole site with Lewis bases (LB = NH and NCH) and anions (X = F, Cl, Br, and I) were comparatively investigated using methods. The energetic features outlined remarkable interaction ( ) and binding ( ) energies for all complexes aligned from -5.65 to -91.
View Article and Find Full Text PDFOrg Lett
August 2025
Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
We report here a concise and regioselective synthesis of benzofulvene derivatives via an iodine(III)-mediated cyclization cascade of diynes. For 1,2-dialkynylbenzene substrates, the iodanylative cyclization is accompanied by triflation or fluorination, depending on the iodine(III) reagent, affording stereodefined benzofulvene derivatives. In contrast, the reaction of 1,6-diyne substrates is terminated by intramolecular Friedel-Crafts cyclization to deliver fused benzofulvene frameworks.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Electrophilic halogenation is a fundamentally useful transformation, and Lewis basic selenium catalysts together with N-haloimides are known to promote the reaction under mild conditions. Selenourea is a frequently used platform for the Lewis base catalyst design. In literature, it is generally believed that the Lewis basic selenium can form a Lewis adduct with the halogen as the active halogenating species.
View Article and Find Full Text PDFMolecules
July 2025
School of Chemistry and Chemical Engineering, Lanzhou Jiaotong University, Lanzhou 730070, China.
Diaryliodonium salts are an important part of hypervalent iodine chemistry, owing to their highly electrophilic character, non-toxicity, and air and moisture stability, have been identified as an important arylating agent. It has been widely applied in the synthesis of natural products, drugs, and bioactive molecules bearing active α-arylation carbonyl units. Within the domain of α-arylation of carbonyl compounds using diaryliodonium salts, there is a notable absence in the literature of a comprehensive compilation dedicated to exclusive arylation processes involving these compounds.
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