Abstract
The well-known lanthanide-binding motif, 2,6-pyridinedicarboxamide, has been functionalised with peripheral substituents using copper-catalysed azide alkyne coupling (CuAAC) to develop new symmetrical ‘clicked’ N2,N6-bis((1-(X)-1H-1,2,3,-triazol-4-yl)methyl)pyridine- 2,6-dicarboxamide (where X = ethyl (1) benzyl (2) and 2-naphthyl (3)). These ligands have been successfully coordinated with trivalent lanthanide ions (europium, terbium, and lanthanum) forming [Ln(L)3](CF3SO3)3 complexes. The ligands act as effective antennae for Eu3+ and Tb3+ complexes, which exhibit the characteristic sensitised emission profiles. The ability of 1–3 to assemble into 1:3 M:L systems in solution was investigated using UV-Vis, fluorescence, and NMR. Finally, density functional calculations of the ground state La3+ complexes have been carried out and show similar geometry and coordination parameters to those with available crystallographic data. The facile and modular synthesis of these ‘clicked’ PDC-based ligands makes these compounds excellent candidates for luminescent supramolecular materials development.
Original language | English |
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Pages (from-to) | 160-173 |
Number of pages | 14 |
Journal | Supramolecular Chemistry |
Volume | 33 |
Issue number | 5 |
DOIs | |
Publication status | Published - 18 Aug 2021 |
Bibliographical note
Funding Information:We would like to thank Ian Stewart for collecting Mass Spec., the New Zealand Ministry of Business, Innovation and Employment and the Royal Society Te Apārangi, for a Catalyst: Seeding fund.
Publisher Copyright:
© 2021 Informa UK Limited, trading as Taylor & Francis Group.
Keywords
- 2,6-pyridinedicarboxamide
- Lanthanides
- luminescent materials
- supramolecular architectures
- triazole ‘click’ chemistry and
ASJC Scopus subject areas
- General Chemistry