Romito, Deborah, Biot, Nicolas, Babudri, Francesco and Bonifazi, Davide ![]() |
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Abstract
In this work, chalcogen functionalized dithiophenes, equipped on both extremities with chalcogen-bonding recognition heterocycles, have been prepared following two synthetic pathways. The insertion of the chalcogenazolo[5,4-β]pyridine allows the control of the organization at the solid state. X-Ray diffraction analysis of the single crystals, showed that the Te-doped derivatives give the most persistant assemblies, with the molecules arranging at solid-state in wire-like polymeric structures through Te⋯N interactions. As expected, the introduction of the Se and Te atoms, dramatically decreases the emission properties, with the Te-bearing congeners being virtually non emissive.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | Royal Society of Chemistry |
ISSN: | 1144-0546 |
Date of First Compliant Deposit: | 12 May 2020 |
Date of Acceptance: | 3 April 2020 |
Last Modified: | 12 Nov 2024 05:00 |
URI: | https://orca.cardiff.ac.uk/id/eprint/131590 |
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