4.7 Article

Carborane-based heteromolecular extended networks driven by directional C-Te⋯N chalcogen bonding interactions

Journal

CHEMICAL COMMUNICATIONS
Volume 59, Issue 92, Pages 13727-13730

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc04338j

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We demonstrate that the presence of linear ditopic neutral Lewis bases can drive the formation of 1D extended supramolecular networks with o-closo-(TeMe)2carborane, through efficient C-TeMIDLINE HORIZONTAL ELLIPSISN chalcogen bonding interactions.
We demonstrate that o-closo-(TeMe)2carborane directs, in the presence of linear ditopic neutral Lewis bases, the formation of co-crystals with 1D extended supramolecular networks. Specifically, the network formation is systematically stabilized by short and quasi-linear C-TeMIDLINE HORIZONTAL ELLIPSISN chalcogen-bonding (ChB) interactions. In sum, we report efficient carborane-based tectons to rationally design high-dimensional neutral heteromolecular networks. Bis(telluromethyl)-o-carborane directs, in the presence of linear ditopic neutral Lewis bases, the formation of 1D extended supramolecular networks driven by efficient C-TeMIDLINE HORIZONTAL ELLIPSISN chalcogen bonding interactions.

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