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Clathrate formation and molecular recognition by novel chalcogen-cyano interactions in tetracyanoquinodimethanes fused with thiadiazole and selenadiazole rings

TLDR
In this paper, the intermolecular contacts between chalcogen atoms and cyano lone pairs were found to stabilize the crystalline state by electrostatic interaction, which is one of the sources of the directionality in crystal paccking of organic molecules and causes the formation of various types of inclusion lattices in the charge transfer (CT) crystals of I-3.
Abstract
The intermolecular contacts between chalcogen atoms and cyano lone pairs were found to stabilize the crystalline state by electrostatic interaction. This interaction is one of the sources of the directionality in crystal paccking of organic molecules and causes the formation of various types of inclusion lattices in the charge-transfer (CT) crystals of I-3. By using highly selective formation of CT crystals with substituted aromatic hydrocarbons, particular isomers such as p-xylene or 2,6-dimethylnaphthalene (2,6-DMN) could be separated from the corresponding isomer mixtures

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Supramolekulare Synthone für das Kristall‐Engineering ‐ eine neue organische Synthese

TL;DR: The supramolekulare Beschreibung einer Kristall-strategies as mentioned in this paper is the hochste Form eines Suprabulekuls, and sein von chemischen and geometrischen Faktoren bestimmter Zusammenbau aus Molekulen ist das perfekte Beispiel fur molekular Erkennung im festen Zustand.
Journal ArticleDOI

Chalcogen bonding in synthesis, catalysis and design of materials

TL;DR: This Perspective presents some demonstrative experimental observations in which chalcogen bonding is crucial for synthetic transformations, crystal engineering, catalysis and design of materials as synthons/tectons.
Journal ArticleDOI

The nature of the supramolecular association of 1,2,5-chalcogenadiazoles.

TL;DR: In this paper, the relativistic density functional theory was applied to the 1,2,5-chalcogenadiazoles and showed that tellurium derivatives possess the strongest association energies; these are so large that the binding strength is comparable to some hydrogen bonds.
Journal ArticleDOI

2,1,3‐Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules

TL;DR: The 2,1,3-Benzothiadiazole (BTD) is one of the most important nuclei used in the chemistry of photoluminescent compounds and applicable for light technology as discussed by the authors.
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