Özay, ÖzgürYildirim, MehmetOzay, Hava2025-01-272025-01-2720171042-65071563-5325https://doi.org/10.1080/10426507.2016.1237950https://hdl.handle.net/20.500.12428/22453Three novel fully substituted urea derivative cyclotriphosphazene compounds 5-7 were synthesized by alkyne-azide 1,3-dipolar cycloaddition reaction of propargyl substituted ureas 2-4 with hexaazide substituted cyclotriphosphazene 1 in the presence of Cu(I) catalyst. All compounds were characterized with spectroscopic techniques such as FT-IR, H-1, C-13, and P-31 nuclear magnetic resonance and mass spectroscopy. Also, the usefulness of compounds 5-7 as anion carriers was investigated by H-1 NMR spectroscopy. For this purpose, H-1 NMR spectra of compounds 5-7 were recorded in the presence of tetrabutylammonium fluoride in DMSO-d(6). It was determined, that the urea protons in the compounds interact with fluoride.eninfo:eu-repo/semantics/closedAccessAzide-alkyne cycloadditioncyclotriphosphazeneureaclick reactionhexapodal compoundArticle192330731510.1080/10426507.2016.1237950Q4WOS:0003951288000102-s2.0-85007377531Q3