4.7 Article

Facile two-step synthesis of para-dithienopyrazines

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 10, Issue 15, Pages 3726-3731

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3qo00684k

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This work describes a convenient route for the synthesis of para-dithienopyrazines from readily available starting materials. A cascade of nucleophilic aromatic substitution and subsequent bidirectional hydrothiolation of alkynes was used as a key step. In total, seven new target compounds were synthesized and investigated regarding their photophysical properties. In solution, these molecules act as blue emitters, which turn to green upon addition of an acid, demonstrating their potential use as proton sensors.
N-Heteropolycyclic compounds are valuable building blocks in organic electronic devices. In this work, a convenient route for the synthesis of para-dithienopyrazines from readily available starting materials is described. A cascade of nucleophilic aromatic substitution and subsequent bidirectional hydrothiolation of alkynes was used as a key step. In total, seven new target compounds were synthesized and investigated regarding their photophysical properties. In solution, these molecules act as blue emitters, which turn to green upon addition of an acid, which demonstrates their potential use as proton sensors.

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