Supphachok ChanmungkalakulVuthichai ErvithayasupornPatcharaporn BoonkittiAlisa PhuekphongNicha PrigyaiSumana KladsomboonSuda KiatkamjornwongChulalongkorn UniversityMahidol UniversityFRST2019-08-232019-08-232018-01-01Chemical Science. Vol.9, No.40 (2018), 7753-776520416539204165202-s2.0-85055885283https://repository.li.mahidol.ac.th/handle/20.500.14594/45520© The Royal Society of Chemistry. Anthracene-conjugated octameric silsesquioxane (AnSQ) cages, prepared via Heck coupling between octavinylsilsesquioxane (OVS) and 9-bromoanthracene, thermodynamically display intramolecular excimer emissions. More importantly, these hosts are sensitive to each anionic guest, thereby resulting in change of anthracene excimer formation, displaying the solvent-dependent fluorescence and allowing us to distinguish up to four ions such as F−, OH−, CN− and PO43− by fluorescence spectroscopy. Depending on the solvent polarity, for example, both F− and CN− quenched the fluorescence emission intensity in THF, but only F− could enhance the fluorescence in all other solvents. The presence of PO43− results in fluorescence enhancements in high polarity solvents such as DMSO, DMF, and acetone, while OH− induces enhancements only in low polarity solvents (e.g. DCM and toluene). A picture of the anion recognizing ability of AnSQ was obtained through principal component analysis (PCA) with NMR and FTIR confirming the presence of host-guest interactions. Computational modeling studies demonstrate the conformation of host-guest complexation and also the change of excimer formation. Detection of F−, CN− and OH− by AnSQ hosts in THF is noticeable with the naked eye, as indicated by strong color changes arising from charge transfer complex formation upon anion addition.Mahidol UniversityChemistryArticleSCOPUS10.1039/c8sc02959h