Literature DB >> 26809623

Halogen Bonding in Hypervalent Iodine Compounds.

Luca Catalano1, Gabriella Cavallo1, Pierangelo Metrangolo2, Giuseppe Resnati3, Giancarlo Terraneo1.   

Abstract

Halogen bonds occur when electrophilic halogens (Lewis acids) attractively interact with donors of electron density (Lewis bases). This term is commonly used for interactions undertaken by monovalent halogen derivatives. The aim of this chapter is to show that the geometric features of the bonding pattern around iodine in its hypervalent derivatives justify the understanding of some of the longer bonds as halogen bonds. We suggest that interactions directionality in ionic and neutral λ(3)-iodane derivatives is evidence that the electron density distribution around iodine atoms is anisotropic, a region of most positive electrostatic potential exists on the extensions of the covalent bonds formed by iodine, and these positive caps affect, or even determine, the crystal packing of these derivatives. For instance, the short cation-anion contacts in ionic λ(3)-iodane and λ(5)-iodane derivatives fully match the halogen bond definition and geometrical prerequisites. The same holds for the short contacts the cation of ionic λ(3)-iodanes forms with lone-pair donors or the short contacts given by neutral λ(3)-iodanes with incoming nucleophiles. The longer and weaker bonds formed by iodine in hypervalent compounds are usually called secondary bondings and we propose that the term halogen bond can also be used. Compared to the term secondary bond, halogen bond may possibly be more descriptive of some bonding features, e.g., its directionality and the relationships between structure of interacting groups and interaction strength.

Entities:  

Keywords:  Crystal engineering; Halogen bond; Hypervalent iodine; Supramolecular chemistry

Year:  2016        PMID: 26809623     DOI: 10.1007/128_2015_666

Source DB:  PubMed          Journal:  Top Curr Chem        ISSN: 0340-1022


  8 in total

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Journal:  J Am Soc Mass Spectrom       Date:  2017-07-17       Impact factor: 3.109

2.  Zwitterionic iodonium species afford halogen bond-based porous organic frameworks.

Authors:  Natalia S Soldatova; Pavel S Postnikov; Daniil M Ivanov; Oleg V Semyonov; Olga S Kukurina; Olga Guselnikova; Yusuke Yamauchi; Thomas Wirth; Viktor V Zhdankin; Mekhman S Yusubov; Rosa M Gomila; Antonio Frontera; Giuseppe Resnati; Vadim Yu Kukushkin
Journal:  Chem Sci       Date:  2022-04-12       Impact factor: 9.969

3.  Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts.

Authors:  Gabriella Cavallo; Jane S Murray; Peter Politzer; Tullio Pilati; Maurizio Ursini; Giuseppe Resnati
Journal:  IUCrJ       Date:  2017-05-10       Impact factor: 4.769

4.  Substituent Effects in Multivalent Halogen Bonding Complexes: A Combined Theoretical and Crystallographic Study.

Authors:  Antonio Bauzá; David Quiñonero; Antonio Frontera
Journal:  Molecules       Date:  2017-12-22       Impact factor: 4.411

5.  An Expedient Method for the Umpolung Coupling of Enols with Heteronucleophiles.

Authors:  Víctor García-Vázquez; Alba Carretero Cerdán; Amparo Sanz-Marco; Enrique Gómez-Bengoa; Belén Martín-Matute
Journal:  Chemistry       Date:  2022-06-17       Impact factor: 5.020

6.  Substituent Effects on the [N-I-N](+) Halogen Bond.

Authors:  Anna-Carin C Carlsson; Krenare Mehmeti; Martin Uhrbom; Alavi Karim; Michele Bedin; Rakesh Puttreddy; Roland Kleinmaier; Alexei A Neverov; Bijan Nekoueishahraki; Jürgen Gräfenstein; Kari Rissanen; Máté Erdélyi
Journal:  J Am Chem Soc       Date:  2016-06-17       Impact factor: 15.419

7.  Hypervalent Iodine(III) Compounds as Biaxial Halogen Bond Donors.

Authors:  Flemming Heinen; Elric Engelage; Christopher J Cramer; Stefan M Huber
Journal:  J Am Chem Soc       Date:  2020-04-29       Impact factor: 15.419

8.  Halogen Complexes of Anionic N-Heterocyclic Carbenes.

Authors:  Jenni Frosch; Marvin Koneczny; Thomas Bannenberg; Matthias Tamm
Journal:  Chemistry       Date:  2020-12-21       Impact factor: 5.236

  8 in total

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