| Literature DB >> 35706420 |
Osama El-Zubir1, Pablo Rojas Martinez1, Gema Dura1,2, Lamia L G Al-Mahamad3, Thomas Pope1, Thomas J Penfold1, Lewis E Mackenzie4, Robert Pal4, Jackie Mosely4, Fabio Cucinotta1, Liam F McGarry1, Benjamin R Horrocks1, Andrew Houlton1.
Abstract
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. This journal is © The Royal Society of Chemistry.Entities:
Year: 2022 PMID: 35706420 PMCID: PMC9097859 DOI: 10.1039/d2tc00366j
Source DB: PubMed Journal: J Mater Chem C Mater ISSN: 2050-7526 Impact factor: 8.067