Halogen bonds of halonium ions
Open Access
- 25 March 2020
- journal article
- review article
- Published by Royal Society of Chemistry (RSC) in Chemical Society Reviews
- Vol. 49 (9) , 2688-2700
Abstract
Due to their electron deficiency, halonium ions act as particularly strong halogen bond donors. By accepting electrons in both lobes of their empty p-orbital, they are capable of simultaneously interacting with two Lewis bases. The interaction presumes the formation of three molecular orbitals and is accordingly typically entitled as a three-center halogen bond. In analogy to the [D–H–D]+ hydrogen bonds, which are at times entitled as short and strong bonds, the [D–X–D]+ halogen bonds of halonium ions show Bondi normalized interatomic distances of 0.6–0.7 and possess both charge transfer and electrostatic characteristics. The three-center halogen bond of halonium ions shows distinct differences in its properties from coordinative bonds of transition metals and is therefore applicable as a complementary synthon in supramolecular chemistry. The three-center halogen bond modulates the reactivity of halonium ions and is hence a useful tool for synthetic organic chemistry. Following the discussion of the nature and properties of halonium ions’ halogen bonds, this tutorial review provides an overview of their current applications to stimulate future developments.Keywords
Funding Information
- Vetenskapsrådet (2016-03602)
- Svenska Forskningsrådet Formas (2017-01173)
This publication has 58 references indexed in Scilit:
- Solvent effects on 15N NMR coordination shiftsMagnetic Resonance in Chemistry, 2012
- Solvent effects on halogen bond symmetryCrystEngComm, 2012
- Halogen bonding in solutionChemical Society Reviews, 2012
- Isotope-Induced Desymmetrization Can Mimic Isotopic Perturbation of Equilibria. On the Symmetry of Bromonium Ions and Hydrogen BondsJournal of the American Chemical Society, 2011
- Soft–Soft Interactions Involving Iodoselenophosphonium Cations: Supramolecular Structures of Iodine Adducts of Bulky Trialkylphosphane SelenidesEuropean Journal of Inorganic Chemistry, 2008
- Bis(pyridine)iodonium Tetrafluoroborate (IPy2BF4): A Versatile Oxidizing ReagentChemistry – A European Journal, 2004
- Coordination and oxidation of phosphine selenides with iodine: from cation pairs [(R3PSe)2I+]2 to (iodoseleno)phosphonium ions [R3PSeI]+ existing as guests in polyiodide matricesChemical Communications, 1999
- Conductivity, FT-Raman spectra, and x-ray crystal structures of two novel [D2I]In (n = 3 and D = N-methylbenzothiazole-2(3H)-selone; n = 7 and D = N-methylbenzothiazole-2(3H)-thione) iodonium salts. First example of I-.3I2 heptaiodideInorganic Chemistry, 1993
- I(py)2BF4, a New Reagent in Organic Synthesis: General Method for the 1,2‐Iodofunctionalization of OlefinsAngewandte Chemie International Edition, 1985
- Crystal and molecular structure of bis(quinoline)bromine perchlorateJ. Chem. Soc., Dalton Trans., 1975