Literature DB >> 25805141

Halogen bonding in solution.

Anna-Carin C Carlsson1, Alberte X Veiga, Máté Erdélyi.   

Abstract

Because of its expected applicability for modulation of molecular recognition phenomena in chemistry and biology, halogen bonding has lately attracted rapidly increasing interest. As most of these processes proceed in solution, the understanding of the influence of solvents on the interaction is of utmost importance. In addition, solution studies provide fundamental insights into the nature of halogen bonding, including, for example, the relative importance of charge transfer, dispersion, and electrostatics forces. Herein, a selection of halogen bonding literature is reviewed with the discussion focusing on the solvent effect and the electronic characteristics of halogen bonded complexes. Hence, charged and neutral systems together with two- and three-center bonds are presented in separate sub-sections. Solvent polarity is shown to have a slight stabilizing effect on neutral, two-center halogen bonds while strongly destabilizes charged, two-center complexes. It does not greatly influence the geometry of three-center halogen bonds, even though polar solvents facilitate dissociation of the counter-ion of charged three-center bonds. The charged three-center bonds are strengthened by increased environment polarity. Solvents possessing hydrogen bond donor functionalities efficiently destabilize all types of halogen bonds, primarily because of halogen vs hydrogen bond competition. A purely electrostatic model is insufficient for the description of halogen bonds in polar systems whereas it may give reasonable correlation to experimental data obtained in noninteracting, apolar solvents. Whereas dispersion plays a significant role for neutral, two-center halogen bonds, charged halogen bond complexes possess a significant charge transfer characteristic.

Entities:  

Year:  2015        PMID: 25805141     DOI: 10.1007/128_2014_607

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


  4 in total

1.  Benchmarking DFT methods with small basis sets for the calculation of halogen-bond strengths.

Authors:  Antti Siiskonen; Arri Priimagi
Journal:  J Mol Model       Date:  2017-02-04       Impact factor: 1.810

2.  Halogen Bond Asymmetry in Solution.

Authors:  Sofia Lindblad; Krenare Mehmeti; Alberte X Veiga; Bijan Nekoueishahraki; Jürgen Gräfenstein; Máté Erdélyi
Journal:  J Am Chem Soc       Date:  2018-10-04       Impact factor: 15.419

3.  Tunable chiral triazole-based halogen bond donors: assessment of donor strength in solution with nitrogen-containing acceptors.

Authors:  Anna Peterson; Mikk Kaasik; Andrus Metsala; Ivar Järving; Jasper Adamson; Tõnis Kanger
Journal:  RSC Adv       Date:  2019-04-15       Impact factor: 4.036

4.  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

  4 in total

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