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Chalcogen Bond versus Halogen Bond: Changing Contributions in Determining the Crystal Packing of Dihalobenzochalcogenadiazoles

Yusuke Ishigaki, Kai Shimomura, Kota Asai, Takuya Shimajiri, Tomoyuki Akutagawa, Takanori Fukushima, Takanori Suzuki

2022Bulletin of the Chemical Society of Japan20 citationsDOI

Abstract

Abstract In the crystals of 4,7-dihalobenzo[c][1,2,5]chalcogenadiazoles, the molecules are connected by two competing secondary bonding interactions: chalcogen bond (ChB) and halogen bond (HaB). Because the strengths of ChB and HaB change according to the kind of chalcogen (E: S, Se, Te) and halogen (X: Cl, Br, I), their relative contributions in determining the crystal packing can also change. Six newly determined crystal structures as well as 3 previously reported structures can be categorized into two groups: ChB-dominant and HaB-dominant structures. HaB in which X = I is strong enough to dictate the crystal packing of compounds with E = S and Se, but not where E = Te, whereas HaB in which X = Cl or Br has little effect on ChB-dominant molecular networks in crystals. The observed changing contributions of ChB and HaB may be useful for designing new supramolecular synthons for crystal engineering.

Topics & Concepts

ChalcogenChemistrySynthonHalogen bondHeteroatomCrystallographyHalogenCrystal (programming language)Crystal engineeringCrystal structureSupramolecular chemistryAtom (system on chip)MoleculeStereochemistryOrganic chemistryRing (chemistry)Embedded systemProgramming languageComputer scienceAlkylCrystallography and molecular interactionsCrystal structures of chemical compoundsStructural and Chemical Analysis of Organic and Inorganic Compounds
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