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Circularly polarised luminescence in an RNA-based homochiral, self-repairing, coordination polymer hydrogel
The aqueous equimolar reaction of Ag(i) ions with the thionucleoside enantiomer (−)6-thioguanosine, ((−)6tGH), yields a one-dimensional coordination polymer {Ag(−)tG}(n), the self-assembly of which generates left-handed helical chains. The resulting helicity induces an enhanced chiro-optical respons...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097859/ https://www.ncbi.nlm.nih.gov/pubmed/35706420 http://dx.doi.org/10.1039/d2tc00366j |
Sumario: | The aqueous equimolar reaction of Ag(i) ions with the thionucleoside enantiomer (−)6-thioguanosine, ((−)6tGH), yields a one-dimensional coordination polymer {Ag(−)tG}(n), the self-assembly of which generates left-handed helical chains. The resulting helicity induces an enhanced chiro-optical response compared to the parent ligand. DFT calculations indicate that this enhancement is due to delocalisation of the excited state along the helical chains, with 7 units being required to converge the calculated CD spectra. At concentrations ≥15 mmol l(−1) reactions form a sample-spanning hydrogel which shows self-repair capabilities with instantaneous recovery in which the dynamic reversibility of the coordination chains appears to play a role. The resulting gel exhibits circularly polarised luminescence (CPL) with a large dissymmetry factor of −0.07 ± 0.01 at 735 nm, a phenomenon not previously observed for this class of coordination polymer. |
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