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Journal ArticleDOI

Anion coordination and anion-templated assembly under halogen bonding control

TLDR
In this article, a selected set of halogen-bonded architectures have been discussed, where anions function as halogen bonding acceptors, and their ability to afford a wide variety of supramolecular architectures in a rational and predictable way.
Abstract
This highlight discusses a selected set of halogen-bonded architectures reported in the literature wherein anions function as halogen bonding acceptors. Some of these architectures have been assembled purposefully, others have been obtained serendipitously. This paper is perhaps the first attempt to prove the effectiveness of halogen bonding in anion coordination and anion-templated assembly. A corollary of this attempt is that anions are particularly robust tectons in halogen bonding driven self-assembly processes. The focus here is particularly on halide anions and their ability to afford a wide variety of supramolecular architectures in a rational and predictable way. A brief inventory of other anions and their behaviour in self-assembly processes based on halogen bonding is also given.

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Journal ArticleDOI

The Halogen Bond

TL;DR: The specific advantages brought up by a design based on the use of the halogen bond will be demonstrated in quite different fields spanning from material sciences to biomolecular recognition and drug design.
Journal ArticleDOI

Recent advances in crystal engineering

TL;DR: The 10th edition of CrystEngComm as mentioned in this paper highlighted the state-of-the-art of crystal engineering and new trends and developing areas in crystal engineering, such as intermolecular interactions, metal-organic frameworks or coordination polymers; polymorphism and solvates.
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The halogen bond in the design of functional supramolecular materials: recent advances.

TL;DR: The tunable interaction strengths provide tools for understanding light-induced macroscopic motions in photoresponsive azobenzene-containing polymers, and the directionality renders halogen bonding useful in the design on functional supramolecular liquid crystals and gel-phase materials.
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Halogen Bonding: An Interim Discussion

TL;DR: This discussion addresses the origins of σ holes, the factors that govern the magnitudes of their electrostatic potentials, and the properties of the resulting complexes with negative sites, and points out that σ-hole interactions are not limited to halogens, but can also involve covalently bonded atoms of Groups IV-VI.
References
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Journal ArticleDOI

Halogen bonding: the σ-hole

TL;DR: In this paper, the authors carried out a natural bond order B3LYP analysis of the molecules CF(3)X, with X = F, Cl, Br and I. The results showed that the Cl and Br atoms in these molecules closely approximate the [Formula: see text] configuration, where the z-axis is along the R-X bond.
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Halogen Bonding Based Recognition Processes: A World Parallel to Hydrogen Bonding †

TL;DR: The main features of the interaction are given, and the close similarity with the hydrogen bonding will become apparent, and some heuristic principles are presented to develop a rational crystal engineering based on halogen bonding.
Journal ArticleDOI

Halogen Bonding in Supramolecular Chemistry

TL;DR: In this article, the energy and geometrical features of the interaction are described along with the atomic characteristics that confer molecules with the specific ability to interact through this interaction, and some principles are presented for crystal engineering based on halogen-bonding interactions.
Journal ArticleDOI

An overview of halogen bonding

TL;DR: An explanation for its occurrence in terms of a region of positive electrostatic potential present on the outermost portions of some covalently-bonded halogen atoms is presented.

The halogen bonding in supramolecular chemistry

TL;DR: The energetic and geometrical features of the interaction are described along with the atomic characteristics that confer molecules with the specific ability to interact through this interaction.
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